BACKGROUND OF THE INVENTION The herpesviruses comprise a large family of double stranded DNA viruses. They are also a source of the most common viral illnesses in man. Eight of the herpes viruses, herpes simplex virus types 1 and 2 (HSV-1 and HSV-2), varicella zoster virus (VZV), human cytomegalovirus (HCMV), epstein-Barr virus (EBV), and human herpes viruses 6, 7, and 8 (HHV-6, HHV-7, and (HHV-8), have been shown to infect humans.

HSV-1 and HSV-2 cause herpetic lesions on the lips and genitals, respectively.

They also occasionally cause infections of the eye and encephalitis. HCMV causes birth defects in infants and a variety of diseases in immunocompromised patients such as retinitis, pneumonia, and gastrointestinal disease. VZV is the causitive agent of chicken pox and shingles. EBV causes infectious mononucleosis. It can also cause lymphomas in immunocompromised patients and has been associated with Burkitt's lymphoma, nasopharyngeal carcinoma, and Hodgkins disease. HHV-6 is the causitive agent of roseola and may be associated with multiple sclerosis and chronic fatigue syndrome. HHV-7 disease association is unclear, but it may be involved in some cases of roseola. HHV-8 has been associated with Karposi's sarcoma, body cavity based lymphomas, and multiple myeloma.

Due to the unique position of the para-substitutent on the N-phenylmethyl of formula I described herein below, compounds of the present invention demonstrate unexpected activity against the above reference herpesviral infections, particularly, human cytomegaloviral infection.

INFORMATION DISCLOSURE US Patent 5,792,774 discloses oxazino 1, 4-dihydro-4-oxoquinolines useful for the treatment of a large number of diseases modulated by tissue necrosis factor (TNF) or phosphodiesterase IV, includng cytomegalovirus (CMV) infections.

US Patent 4,847,375 discloses 1,8-bridged 4-quinoline-3-carboxylic acids useful as antibacterial agents.

US Patent 5,583,135 discloses heterotricyclic derivatives having a strong immunomodulating activity, anti-inflammatory activity and anti-cancer activity.

The abstract of Japanese Patent JP 10324631-A discloses IgE antibody production inhibitor comprise a pyrido (1, 2,3-del, 4-benzoxazine or a pyrido (1, 2,3,-de)-1,4- benzothiazine derivative.

PCT patent application, PCT/US00/21985 discloses oxazinoquinolones useful for the treatment of viral infections.

SUMMARY OF THE INVENTION The present, invention provides a compound of formula I, I or a pharmaceutically acceptable salt, racemate, solvate, tautomer, optical isomer or prodrug derivative thereof wherein: each X is independently O or S; Y is Cl, F, Br, CN or NO2 ; Rl, R2, R3 and R4 are independently a) hydrogen, b) N3, c) CN, d) fluoro, e) trifluoromethyl, f) aryl, g) het, h) Cl_8 alkyl, optionally substituted with R6 or OR7, or i) Rl and R2 or R3 and R4 together with the carbon to which they are attached form C3 8cycloalkyl or het;

R5 is C1-8alkyl, which may be partially unsaturated and optionally substituted with one to three N3, halo, CN, R6 or R7 ; R6is a) aryl, b) het, c) SOiR8, d) OR8, e) C (=O) ORs, f) C(=O)R8, or g) NR8R9; R7 is a) P (=O) (OR10) 2, b) CO (CH2) jCON (CH3) (CH2) kSO3-M+, c) an amino acid, d) C (=O) C1-6alkyl, optionally substituted by NR10R10, or e) CO (CH2) nCO2H ; R8 and Rg are independently a) hydrogen, b) C3-8cycloalkyl, c) aryl, d) het, or e) C1-8alkyl which is further optionally substituted with one or more aryl, het, halo, CN, CO2R10, SOiR10, OR10, NR10R10, CF3, or C3-8cycloalkyl ; Rio is a) Hor b) C1-8alkyl, optionally substituted with OH or OC1-4alkyl ; Rll and R12 are independently a) hydrogen, b) halo, c) NO2, d) CN, SO iNR8R9, or

g) Cl 8alkyl, which may be partially unsaturated and optionally substituted with one to three N3, halo, CN, R6 or OR7 ; aryl is a phenyl radical, optionally fused with a saturated or unsaturated carbocyclic or heterocyclic ring; at each occurrence, aryl may be substituted with one or more halo, CN, C02Ro, SO ; Rio, ORio, NRloRio, CF3, C3-acycloalkyl, or Cl 4alkyl wherein C1-4alkyl is optionally substituted with ORIO ; het is a four- (4), five- (5), six- (6), or seven- (7) membered saturated or unsaturated heterocyclic ring having 1,2, or 3 heteroatoms selected from the group consisting of O, S, and NW, wherein W is hydrogen, C1-4alkyl C (=O) OC1-4alkyl or absent, wherein het is optionally fused with a benzene ring, a carbcyclic or a heterocyclic ring; at each occurrence, het may be substituted with one or more halo, CN, CO2Rlo, SOiRlo, ORIo, NRloRio, Cl-4alkyl, CF3, C3 gcycloalkyl, oxo or oxine; at each occurrence, a cycloalkyl group may be substituted with C1-4alkyl, OR10, oxo, oxine, or a spiro fused het; i is 0, 1 or 2 ; j is 1,2,3,4,5, or 6 ; k is 1,2,3,4,5, or 6 ; nis 1,2,3,4,5, or6 ; M is sodium, potassium, or lithium; and with the following provisos: a) at least one of Rl, R2, R3 and R4 is other than hydrogen; b) where Rl, R2, R3 and R4 are independently Cl-8 alkyl, at least one of the alkyl groups is substituted with R6 or OR7.

The present invention further provides a pharmaceutical composition comprising a compound of formula I, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier (the composition preferably comprises an effective antiviral amount of the compound or salt).

The present invention further provides a method of treating or preventing a herpesviral infection, comprising administering to a mammal in need of such treatment, a compound of formula (I) or a pharmaceutically acceptable salt thereof.

The present invention further provides a method of treating or preventing a herpesviral infection comprising administering orally, parenterally, topically, rectally, nasally, sublingually or transdermally an effective amount of a compound of claim 1.

The present invention further provides a compound of formula (I) or a pharmaceutically acceptable salt thereof for use in medical treatment.

The present invention further provides the use of a compound of formula (I) or a pharmaceutically acceptable salt thereof to prepare a medicament for treating or preventing a herpesviral infection in a mammal.

The present invention further provides a method for inhibiting a viral DNA polymerase, comprising contacting (in vitro or in vivo) the polymerase with an effective inhibitory amount of a compound of formula I, or a pharmaceutically acceptable salt thereof.

The invention also provides novel intermediates and processes disclosed herein that are useful for preparing compounds of formula I.

DETAILED DESCRIPTION OF THE INVENTION The following definitions are used, unless otherwise described. Halo denotes fluoro, chloro, bromo, or iodo. Alkyl, alkoxy, etc. denote both straight and branched groups; but reference to an individual radical such as"propyl"embraces only the straight chain radical, a branched chain isomer such as"isopropyl"being specifically referred to.

When alkyl can be partially unsaturated, the alkyl chain may comprise one or more (e. g. 1, 2,3, or 4) double or triple bonds in the chain.

The carbon atom content of various hydrocarbon-containing moieties is indicated by a prefix designating the minimum and maximum number of carbon atoms in the moiety, i. e., the prefix Cij indicates a moiety of the integer"i"to the integer"j"carbon atoms, inclusive. Thus, for example, (Cl 3) alkyl refers to alkyl of one to three carbon atoms, inclusive, or methyl, ethyl, propyl and isopropyl, straight and branched forms thereof.

Aryl is a phenyl radical, optionally fused with a saturated or unsaturated carbocyclic or heterocyclic ring. At each occurrence, aryl may be substituted with one or more halo, CN, C02Ro, SOiRio, OR, NRzoRloX CF3, C38cycloalkyl, or Cl 4alkyl wherein Cl 4alkyl is optionally substituted with ORIO.

Het is a four- (4), five- (5), six- (6), or seven- (7) membered saturated or unsaturated heterocyclic ring having 1,2, or 3 heteroatoms selected from the group consisting of O, S,

and NW, wherein W is hydrogen, Cl 4alkyl, C (=O) Oc 4alkyl or absent, wherein het is optionally fused with a benzene ring, a carbcyclic or a heterocyclic ring. At each occurrence, het may be substituted with one or more halo, CN, C02Rlo, SO ; Rlo, ORIO ; NRloRio, C1-4alkYl, CF3, C3-8cycloalkyl, oxo or oxine; The term"het"also includes piperidinyl, morpholinyl, thiomorpholinyl, piperazinyl, N-CI 4alky substituted piperazinyl such as 4-methyl piperazinyl, pyrrolidinyl, pyridyl, imidazolyl, N-Cs 4alky substituted imidazol such as 1-methyl-lH-imidazol, azetidyl, tetrahydrofuranyl, dioxolanyl, imidazolidinyl, oxathiolanyl, oxazolidinyl, pyran, thiopyran, tetrahydropyran or tetrahydrothiopyran, thiophene, furan, pyrazoline, pyrimidine, 2-pyridyl, 3-pyridyl, 4-pyridyl, 2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl, 3-pyridazinyl, 4- pyridazinyl, 3-pyrazinyl, 2-quinolyl, 3-quinolyl, 1-isoquinolyl, 3-isoquinolyl, 4-isoquinolyl, 2-quinazolinyl, 4-quinazolinyl, 2-quinoxalinyl, 1-phthalazinyl, 4-oxo-2-imidazolyl, 2- imidazolyl, 4-imidazolyl, 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 3-pyrazolyl, 4-pyrazolyl, 5-pyrazolyl, 2-oxazolyl, 4-oxazolyl, 4-oxo-2-oxazolyl, 5-oxazolyl, 4,5,-dihydrooxazole, 1,2,3-oxathiole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,2,5-oxadiazole, 1,3,4-oxadiazole, 2- thiazolyl, 4-thiazolyl, 5-thiazolyl, 3-isothiazole, 4-isothiazole, 5-isothiazole, 2-indolyl, 3- indolyl, 3-indazolyl, 2-benzoxazolyl, 2-benzothiazolyl, 2-benzimidazolyl, 2-benzofuranyl, 3-benzofuranyl, benzoisothiazole, benzisoxazole, 2-furanyl, 3-furanyl, 2-thienyl, 3-thienyl, 2-pyrrolyl, 3-pyrrolyl, 3-isopyrrolyl, 4-isopyrrolyl, 5-isopyrrolyl, 1,2,3,-oxathiazole-1-oxide, 1, 2,4-oxadiazol-3-yl, 1, 2, 4-oxadiazol-5-yl, 5-oxo-1, 2,4-oxadiazol-3-yl, 1, 2,4-thiadiazol-3- yl, 1, 2,4-thiadiazol-5-yl, 3-oxo-1, 2,4-thiadiazol-5-yl, 1, 3,4-thiadiazol-5-yl, 2-oxo-1,3,4- thiadiazol-5-yl, 1, 2,4-triazol-3-yl, 1, 2,4-triazol-5-yl, 1, 2,3,4-tetrazol-5-yl, 5-oxazolyl, 1- pyrrolyl, 1-pyrazolyl, 1,2,3-triazol-1-yl, 1,2,4-triazol-1-yl, 1-tetrazolyl, 1-indolyl, 1- indazolyl, 2-isoindolyl, 7-oxo-2-isoindolyl, l-purinyl, 3-isothiazolyl, 4-isothiazolyl and 5- isothiazolyl, 1,3,4,-oxadiazole, 4-oxo-2-thiazolinyl, or 5-methyl-1, 3,4-thiadiazol-2-yl, thiazoledione, 1,2,3,4-thiatriazole, 1,2,4-dithiazolone. Each of these moieties may be substituted as appropriate.

"Amino acid,"includes a residue of natural amino acid (e. g. Ala, Arg, Asn, Asp, Cys, Glu, Gln, Gly, His, Hyl, Hyp, Ile, Leu, Lys, Met, Phe, Pro, Ser, Thr, Trp, Tyr, and Val) in D or L form, as well as unnatural amino acids (e. g. phosphoserine, phosphothreonine, phosphotyrosine, hydroxyproline, gamma-carboxyglutamate ; hippuric acid, octahydroindole-2-carboxylic acid, statine, 1, 2,3,4,-tetrahydroisoquinoline-3-carboxylic acid, penicillamine, ornithine, citruline,-methyl-alanine, para-benzoylphenylalanine,

phenylglycine, propargylglycine, sarcosine, and tert-butylglycine). An amino acid can conveniently be linked to the remainder of a compound of formula I through the carboxy terminus, the amino terminus, or through any other convenient point of attachment, such as, for example, through the sulfur of cysteine. In particular, an amino acid can conveniently be linked to the remainder of a compound of formula I through the carboxy terminus.

Mammal denotes human and animals, specifically including food animals and companion animals.

It will be appreciated by those skilled in the art that compounds of the invention have one or more achiral center and be isolated in optically active and racemic forms.

Some compounds may exhibit polymorphism. It is to be understood that the present invention encompasses any racemic, optically-active, polymorphic, tautomeric, or stereoisomeric form, or mixture thereof, of a compound of the invention, which possesses the useful properties described herein, it being well known in the art how to prepare optically active forms (for example, by resolution of the racemic form by recrystallization techniques, by synthesis from optically-active starting materials, by chiral synthesis, or by chromatographic separation using a chiral stationary phase) and how to determine antiviral activity using the standard tests described herein, or using other similar tests which are well known in the art.

The compounds of the present invention are generally named according to the IUPAC or CAS nomenclature system. Other nomenclature systems may also be used.

Abbreviations which are well known to one of ordinary skill in the art may be used (e. g.

"Ph"for phenyl,'Me"for methyl,"Et"for ethyl,"h"for hour or hours and"rt"for room temperature).

Specific and preferred values listed below for radicals, substituents, and ranges, are for illustration only; they do not exclude other defined values or other values within defined ranges for the radicals and substituents.

Specifically, the term"Cl 8alkyl,"or"Cs 4alkyl"refers to an alkyl group having one to eight or one to four carbon atoms such as, for example, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, and their isomeric forms thereof.

Specifically, a 5-or 6-membered heterocyclic ring includes piperidinyl, morpholinyl, thiomorpholinyl, piperazinyl, N-Cl 4alky substituted piperazinyl such as 4- methyl piperazinyl, or pyrrolidinyl.

Specifically, a 5-or 6-membered heterocyclic ring includes pyridyl, imidazolyl, N- C1-4alkyl substituted imidazol such as 1-methyl-lH-imidazol.

Specifically, R5 is C1-8alkyl substituted with OR7 or het.

Specifically, R5 is C1-4alkyl substituted with OH.

Specifically, R5 is C1-4alkyl substituted with het.

Specifically, het is morpholinyl or thiomorpholinyl.

Specifically, R5 is 4-morpholiliylmethyl.

Specifically, R5 is CI-8alkyl, optionally substituted with OR9.

Specifically, R5 is C1-8alkyl which is partially unsaturated and optionally substituted with OR9.

Specifically, R5 is propynyl substituted with OH.

Specifically, R5 is 3-hydroxypropyl.

Specifically, R3 and R4 are independently hydrogen.

Specifically, Rl and R2 are independently hydrogen, fluoro, or C1-8 alkyl substituted with R6 or OR7.

Specifically, Rl and R2 are independently hydrogen, fluoro, C1-8 alkyl substituted with R6 or OR7 ; aryl, het, or R1 and R2 together with the carbon to which they are attached form a six- (6) membered cycloalkyl or a het; wherein R6 is het, SOiR8, OR8 or NR8R9 ; wherein R7 is P (=O) (ORIO) 2, CO (CH2) nCON (CH3) (CH2)nSO3- M+, or C (=O) C1-6alkyl, wherein R8 and R9 are independently hydrogen, aryl, het, or C1-8alkyl which is further optionally substituted with one or more aryl, het, halo, C02Rlo, SOiRio, or ORIO ; wherein Rlo is H or C1-4alkyl, optionally substituted with OH.

Specifically, Rl and R2 are indepandetly H, C1-4alkylsubstituted with OR8 wherein R8 is H, or C1-4alkylsubstituted with ORzo.

Specifically, Ri is H; R2 is aryl wherein aryl is optinoally substituted with one or two halo, CN, ORIO, or C1-4alkylsubstituted with OR10.

Specifically, Rl is H; R2 is aryl wherein aryl is fused with a heterocyclic ring.

Specifically, R2 is 1,3-benzodioxolyl or 1,4-benxodioxinyl.

Specifically, Ri is H; R2 is het.

Specifically, het is a five- (5) or six- (6) membered saturated or unsaturated heterocyclic ring having 1,2, or 3 heteroatoms selected from the group consisting of O, S, and NW, wherein W is hydrogen, C1-4alkyl, C (=O) OC1-4alkyl or absent, wherein het may be substituted with one or more halo, C1-4alkyl, CF3, oxo or oxine.

Specifically, het is pyridinyl.

Specifically, het is a five- (5) membered heterocyclic ring.

Specifically, Rl and R2 together with the carbon to which they are attached form a het, wherein het is a five- (5) or six- (6) membered heterocyclic ring having 1,2, or 3 heteroatoms selected from the group consisting of O, S, and NW, wherein W is hydrogen, C1-4alkyl, or C (=O) OC1-4alkyl, wherein het may be substituted with one or more halo, ORIO, C1-4alkyl, CF3, oxo or oxine; more specifically, het is a (6) membered heterocyclic ring; even more specifically, het is pyran, piperdine, or thiopyran.

Specifically, Ri and R2 together with the carbon to which they are attached form a six- (6) membered cycloalkyl ; more specifically, cycloalkyl is optionally substituted with oxo, or ORio.

Specifically, R6 is het, SOiR8, OR8 or NR8R9.

Specifically, R7 is P=O)(OH)2, (P=O)(C1-4akloxy)2, C (=O) C1-6alkyl, or CO (CH2) nCON (CH3) (CH2)nSO2- M+.

Specifically, R8 and R9 are independently hydrogen, aryl, het, or C1-8alkyl which is further optionally substituted with one or more aryl, het, halo, CO2RIO, SOiRio, or OR10 ; Specifically, Rio is H or C1-4alkyl, optionally substituted with OH.

Specifically, R2 is hydrogen, and R1 is C1-8 alkyl substituted with R6 or OR7 ; where R6 is het, Surs, ORs or NR8R9 ; wherein R7 is (P=O) (OCH3) 2, CO (CH2) nCON (CH3) (CH2) nSO3-M+, or C (=O) CH3, Rs and R9 are independently hydrogen, het, or C1-8alkyl, which is optionally substituted with one or two het, CO2R10, SOR10, or OR10 ; Rio is H or C1-4alkyl, optionally substituted with OH.

Specifically, RI, is H, halo, or C1-4alkyl optionally substituted with one to three halo.

Specifically, R12 is H, SOiR8, ORg, C (=O) OR8, C (=O) R8, NR8R9 ; or C1-8alkyl, which may be partially unsaturated and optionally substituted with one to three N3, halo, CN, or R6.

Specifically, RI, and Rl2 are hydrogen.

Specifically, het is piperidinyl, morpholinyl, thiomorpholinyl, piperazinyl, N-Cl 4alky substituted piperazinyl, pyrrolidinyl, pyridyl, imidazolyl, or N-Cl4alky substituted imidazol.

Specifically, Ri, R2, R3 and R4 are independently hydrogen, hydroxymethyl, morpholinylmethyl, (pyridinylmethyl) aminomethyl, (dimethylamino) methyl,

(hydroxyethyl) sulfanylmethyl, (1-methyl-lH-imidazol-2-yl) sulfanylmethyl,- CH20CO (CH2) 6CON (CH3) (CH2) 2S03-M+,-CH20C (=O) CH3, (4-methyl-1- piperazinyl) methyl, 1-pyrrolidinylmethyl, (2,3-dihydroxypropyl) aminomethyl, (2- hydroxyethyl) aminomethyl, l-piperidinylmethyl, bis (2-hydroxyethyl) aminomethyl, 1H- imidazol-1-ylmethyl, (methylsulfanyl) methyl, (tert-butylsulfanyl) methyl, methylsulfanyl acetate, (2,3-dihydroxypropyl) sulfanylmethyl, phenyl, or fluoro. or CH20P (=O) (OCH3) 2.

Specifically, RI, R2, R3 and R4 are independently hydrogen, hydroxymethyl, morpholinylmethyl, (2-pyridinylmethyl) aminomethyl, (3-pyridinylmethyl) aminomethyl, (dimethylamino) methyl, (2-hydroxyethyl) sulfanylmethyl, (1-methyl-1H-imidazol-2- yl) sulfanylmethyl,-CH20CO (CH2) 6CON (CH3) (CH2) 2SO3-M+,-CH20C (=O) CH3, or CH20P (=O) (OCH3) 2.

Specifically, Ri and R2 are independently hydrogen, R3 and R4 are independently fluoro, phenyl, or C1-8 alkyl substituted with het or OH.

Specifically, Ri is hydrogen and R2 is het.

Specifically, Rl is hydrogen and R2 is 2-pyridinyl, 3-pyridinyl, or 4-pyridinyl.

Specifically, R3 and R4 are independently fluoro or hydroxymethyl.

Specifically, R3 is hydrogen and R4 is phenyl, morpholinylmethyl, or hydroxymethyl.

Specifically, R3 is morpholinylmethyl.

Specifically, a compound of formula I is the following structure I-A ; Specifically, a compound of formula I is the following structure I-B ; Specifically, a compound of formula I is the following structure I-C ;

Specifically, a compound of formula I is the following structure I-D ; Specifically, a compound of formula I is the following structure I-E ; Specifically, a compound of formula I is the following structure I-F ; Specifically, a compound of formula I is the following structure I-G ; Specifically, a compound of formula I is the following structure 1-H ;

Specifically, a compound of formula I is the following structure I-I ; Specifically, a compound of formula I is the following structure I-J ; Specifically, a compound of formula I is the following structure I-K ; Specifically, a compound of formula I is the following structure I-L ; Specifically, a compound of formula I is the following structure I-M ; Specifically, a compound of formula I is the following structure I-N ;

Specifically, a compound of formula I is the following structure 1-0 ; Specifically, a compound of formula I is the following structure I-P ; More specifically, Y is Cl in the formulas I-A to I-P.

Examples of the compounds of the present invention are: a) N- (4-Chlorobenzyl)-2- (hydroxymethyl)-9- (morpholin-4-ylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, b) N- (4-Chlorobenzyl)-2- (R or S)- (hydroxymethyl)-9- (morpholin-4-ylmethyl)-7-oxo- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, c) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2-pyridin-3-yl-2, 3-dihydro- 7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, d) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2-pyridin-4-yl-2, 3-dihydro- 7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide,

e) N- (4-Chlorobenzyl)-9- (mbrpholin-4-ylmethyl)-7-oxo-2-pyridin-2-yl-2, 3-dihydro- 7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, f) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2- (R or S)-pyridin-3-yl-2, 3- dihydro-7H- [1, 4] oxazino [2,3, 4-ij]quinoline-6-carboxamide, g) N- (4-Chlorobenzyl)-2, 9-bis (morpholin-4-ylmethyl)-7-oxo-2,3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, h) 2-[(tert-ButylSulfanyl) methyl]-N-(4-chlorobenzyl)-9-(morpholin-4-ylmethyl)-7-oXo- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, i) N-(4-Chlorobenzyl)-2-{[(2-hdyroxyethyl) sulfanyl] methyl}-9- (morpholin-4- ylmethyl)-7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, j) N- (4-Chlorobenzyl)-2- { [ (1-methyl-1H-imidazol-2-yl) sulfanyl] methyl}-9- (morpholin-4-ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide, k) N-(4-Chlorobenzyl)-9-(morpholin-4-ylmethyl)-7-oxo-2-{[(3- pyridinylmethyl) amino] methyl}-2, 3-dihydro-7H-[1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide, 1) [6- { [ (4-Chlorobenzyl) amino] carbonyl}-9- (morpholin-4-ylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinolin-2-yl] methyl acetate, m) N-(4-Chlorobenzyl)-9-(morpholin-4-ylmethyl)-7-oxo-2-(R or S)-{[(3- pyridinylmethyl) amino] methyl}-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide, n) N- (4-Chlorobenzyl)-2- (3-hydroxyphenyl)-9- (morpholin-4-ylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, o) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2- (R or S)-pyridin-2-yl-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, <BR> <BR> <BR> <BR> p) N- (4-Chlorobenzyl)-2- [3- (hydroxymethyl) phenyl]-9- (morpholin-4-ylmethyl)-7-oxo- 2,3-dihydro-7H- [ 1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, q) N- (4-Chlorobenzyl)-2- [2- (hydroxymethyl) phenyl]-9- (morpholin-4-ylmethyl)-7-oxo- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, r) N- (4-Chlorobenzyl)-2- (1-methyl-lH-imidazol-2-yl)-9- (morpholin-4-ylmethyl)-7- oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, s) N- (4-Chlorobenzyl)-2- (2-furyl)-9- (morpholin-4-ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide,

t) N- (4-Chlorobenzyl)-2- (3-cyanophenyl)-9- (morpholin-4-ylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, <BR> <BR> <BR> u) N- (4-Chlorobenzyl)-2- (3-furyl)-9- (morpholin-4-ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, v) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2-thien-2-yl-2, 3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, w) N- (4-Chlorobenzyl)-2- (3, 5-difluorophenyl)-9- (morpholin-4-ylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, x) 2- (1, 3-Benzodioxol-5-yl)-N- (4-chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2, 3- dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, y) N- (4-Chlorobenzyl)-2- (2, 3-dihydro-1,4-benzodioxin-6-yl)-9- (morpholin-4- ylmethyl)-7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, z) 2- (1, 3-Benzodioxol-4-yl)-N- (4-chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, aa) 2- [3, 5-bis (Methoxymethoxy) phenyl]-N- (4-chlorobenzyl)-9- (morpholin-4-ylmethyl)- 7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, bb) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2-thien-3-yl-2, 3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, cc) N- (4-Chlorobenzyl)-2, 2-bis [(methoxymethoxy) methyl]-9-(morpholin-4-ylmethyl)- 7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, dd) N- [ (4-Chlorophenyl) methyl]-9'- (4-morpholinylmethyl)-4, 7'- dioxospiro [cyclohexane-1,2' (3'H)- [7H] pyrido [1, 2,3-de] [1,4] benzoxazine]-6'- carboxamide, ee) N- [ (4-Chlorophenyl) methyl]-4-hydroxy-9'- (4-morpholinylmethyl)-7'- oxospiro [cyclohexane-1,2' (3'H)- [7H] pyrido [1, 2,3-de] [1,4] benzoxazine]-6'- carboxamide, ff) N- (4-Chlorobenzyl)-3, 9-bis (morpholin-4-ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, gg) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2-phenyl-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, hh) N- (4-Chlorobenzyl)-2, 2-difluoro-9- (morpholin-4-ylmethyl)-7-oxo-2, 3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide,

ii) N-(4-Chlorobenzyl)-2-[(methylsulfanyl) methyl]-9-(morpholin-4-ylmethyl)-7-oxo- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, jj) N-(4-Chlorobenzyl)-2-[(dimethylamino)methyl]-9-(morpholin-4- ylmethyl)-7-oxo- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, kk) N- (4-Chlorobenzyl)-2- [ (4-methyl-l-piperazinyl) methyl]-9- (morpholin-4-ylmethyl)- 7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, 11) Methyl ({[6-{[(4-chlorobenzyl)amino]carbonyl}-9-(morpholin-4-ylmeth yl)-7-oxo- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinolin-2-yl] methyl} thio) acetate, mm) N-(4-Chlorobenzyl)-9-(morpholin-4-ylmethyl)-7-oxo-2-(1-pyrro lidinylmethyl)-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, nn) N-(4-chlorobenzyl)-2-{[(2, 3-dihydroxypropyl) sulfanyl] methyl}-9- (morpholin-4- ylmethyl)-7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, oo) N- (4-Chlorobenzyl)-2- ( [ (2, 3-dihydroxypropyl) amino] methyl}-9- (morpholin-4- ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, pp) N- (4-Chlorobenzyl)-2- { [ (2-hydroxyethyl) amino] methyl}-9-(morpholin-4-ylemthyl)- 7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, qq) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2- (1-piperidinylmethyl)-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, rr) 2- { [bis (2-Hydroxyethyl) amino] methyl}-N- (4-chlorobenzyl)-9- (morpholin-4- ylmethyl)-7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ijlquinoline-6-carboxamide, ss) N-(4-Chlorobenzyl)-9-[(morpholin-4-ylmethyl)-7-oxo-2-{[(2- pyridinylmethyl) amino] methyl}-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide, tt) 2- [ (8-1 [6-1 [ (4-Chlorobenzyl) amino] carbonyl}-9-(morpholin-4-ylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinolin-2-yl] methoxy}-8- oxooctanoyl) (methyl) amino] ethanesulfonic acid sodium salt, uu) [6-{[(4-Chlorobenzyl) amino] carbonyl}-9- (morpholin-4-ylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinolin-2-yl] methyl dimethyl phosphate, vv) N-(4-Chlorobenzyl)-9-(morpholin-4-ylmethyl)-7-oxo-2-{[(4- pyridinylmethyl) amino] methyl}-2, 3-dihydro-7H- [ 1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide, ww) N- (4-Chlorobenzyl)-2- (lH-imidazol-1-ylmethyl)-9- (morpholin-4-ylmethyl)-7-oxo- 2,3-dihydro-7H- [ 1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide,

xx) N-(4-Chlorobenzyl)-2-{[(4-chlorobenzyl) amino] methyl}-9- (morpholin-4-ylmethyl)- 7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, yy) N- (4-Chlorobenzyl)-3- (hydroxymethyl)-9- (morpholin-4-ylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, zz) N- (4-Chlorobenzyl)-2- (4-hydroxyphenyl)-9- (morpholin-4-ylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, aaa) N- (4-Chlorobenzyl)-2- {3- [ (methoxymethoxy) methyl] phenyl}-9- (morpholin-4- ylmethyl)-7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, bbb) N- (4-Chlorobenzyl)-2- {2- [ (methoxymethoxy) methyl] phenyl}-9- (morpholin-4- ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, ccc) N- (4-Chlorobenzyl)-2- (2-hydroxyphenyl)-9- (morpholin-4-ylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, ddd) N- [ (4-Chlorophenyl) methyl]-2,3,5,6-tetrahydro-9'- (4-morpholinylmethyl)-7'- oxospiro [4H-pyran-4, 2' (3'I)- [7H] pyrido [1, 2,3-de] [1,4] benzoxazine]-6'- carboxamide, eee) 1,1-Dimethylethyl 6- [ (4-chlorophenyl) methyl] amino] carbonyl]-9'- (4- morpholinylmethyl)-7'-oxospiro [piperidine-4,2' (3'H)- [7H] pyrido [1, 2,3-de] [1,4]benzoxazine]-1-carboxylate, fff) N- [ (4-Chlorophenyl) methyl]-9'- (4-morpholinylmethyl)-7'-oxospiro [piperidine- 4,2' (3'H)- [7H] pyrido [1, 2,3-de] [1,4] benzoxazine]-6'-carboxamide, ggg) N- (4-Chlorobenzyl)-2, 2-bis (hydroxymethyl)-9- (morpholin-4-ylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, hhh) N- [ (4-Chlorophenyl) methyl]-2', 3', 5', 6'-tetrahydro-9- (4-morpholinylmethyl)-7- oxospiro [7H-pyrido [1, 2,3-de]-1, 4-benzoxazine-2 (3H), 4'- [4H] thiopyran]-6- carboxamide, iii) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-3-phenyl-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, jjj) N- (4-Chlorobenzyl)-3, 3-bis (hydroxymethyl)-9- (3-hydroxy-l-propynyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, kkk) N- (4-Chlorobenzyl)-3, 3-bis (hydroxymethyl)-9- (3-hydroxypropyl)-7-oxo-2, 3- dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, 111) N- (4-Chlorobenzyl)-2- [2- (methoxymethoxy) phenyl]-9- (morpholin-4-ylmethyl)-7- oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide,

mmm) N- (4-Chlorobenzyl)-2- {4- [ (methoxymethoxy) methyl] phenyl}-9- (morpholin-4- ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, nnn) 2- [2, 3-bis (Methoxymethoxy) phenyl]-N- (4-chlorobenzyl)-9- (morpholin-4-yhnethyl)- 7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, ooo) N- [ (4-Chlorophenyl) methyl]-l-methyl-9'- (4-morpholinylmethyl)-7'- oxospiro [piperidine-4,2' (3'H)-[7H]pyrido[1, 2,3-de] [1,4] benzoxazine]-6'- carboxamide, or ppp) N- [ (4-Chlorophenyl) methyl]-9"- (4-morpholinylmethyl) dispiro [1, 3-dioxolane-2,1'- cyclohexane-4', 2" (3"H)- [7H] pyrido [1, 2,3-de] [1,4] benzoxazine]-6"-carboxamide.

Additional examples of the compounds of the present invention are: a) N- (4-Chlorobenzyl)-2- (hydroxymethyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, b) N- (4-Chlorobenzyl)-2- (R or S)- (hydroxymethyl)-9- (morpholin-4-ylmethyl)-7- thioxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, c) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2-pyridin-3-yl-2, 3-dihydro- 7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, d) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2-pyridin-4-yl-2, 3-dihydro- 7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, e) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2-pyridin-2-yl-2, 3-dihydro- 7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2- (R or S)-pyridin-3-yl-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, g) N- (4-Chlorobenzyl)-2, 9-bis (morpholin-4-ylmethyl)-7-thioxo-2, 3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide,. h) 2- [ (tert-Butylsulfanyl) methyl]-N- (4-chlorobenzyl)-9- (morpholin-4-ylmethyl)-7- thioxo-2, 3-dihydrio-7H-[1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, i) N-(4-Chlorobenzyl)-2-{[(2-hydroxyethyl) sulfanyl] methyl}-9- (morpholin-4- ylmethyl)-7-thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, j) N-(4-Chlorobenzyl)-2-{ [(l-methyi-lH-imidazol-2-yl) sulfanyl] methyl}-9- (morpholin-4-ylmethyl)-7-thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6- carboxamide,

k) N-(4-Chlorobenzyl)-9-(morpholin-4-ylmethyl)-7-thioxo-2-{ [(3- pyridinylmethyl) amino] methyl}-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide, 1) [6-{[(4-Chlorobenzyl) amino] carbonyl}-9-(morpholin-4-ylmethyl)-7-thioxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinolin-2-yl] methyl acetate, m) N-(4-Chlorobenzyl)-9-(morpholin-4-ylmethyl)-7-thioxo-2-(R or S)-{[(3- pyridinylmethyl) amino] methyl}-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide, n) N- (4-Chlorobenzyl)-2- (3-hydroxyphenyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, o) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2- (R or S)-pyridin-2-yl-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, p) N- (4-Chlorobenzyl)-2- [3- (hydroxymethyl) phenyl]-9- (morpholin-4-ylmethyl)-7- thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, q) N- (4-Chlorobenzyl)-2- [2- (hydroxymethyl) phenyl]-9- (morpholin-4-ylmethyl)-7- thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, r) N- (4-Chlorobenzyl)-2- (l-methyl-lH-imidazol-2-yl)-9- (morpholin-4-ylmethyl)-7- thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, s) N- (4-Chlorobenzyl)-2- (2-furyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, t) N- (4-Chlorobenzyl)-2- (3-cyanophenyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, u) N- (4-Chlorobenzyl)-2- (3-furyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2, 3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, v) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2-thien-2-yl-2, 3-dihydro- 7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, w) N- (4-Chlorobenzyl)-2- (3, 5-difluorophenyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, <BR> <BR> <BR> <BR> x) 2- (1, 3-Benzodioxol-5-yl)-N- (4-chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo- 2,3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, y) N- (4-Chlorobenzyl)-2- (2, 3-dihydro-1,4-benzodioxin-6-yl)-9- (morpholin-4- ylmethyl)-7-thioxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide,

z) 2- (1, 3-Benzodioxol-4-yl)-N- (4-chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, aa) 2- [3, 5-bis (Methoxymethoxy) phenyl]-N- (4-chlorobenzyl)-9- (morpholin-4-ylmethyl)- 7-thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, bb) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2-thien-3-yl-2, 3-dihydro- 7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, cc) N- (4-Chlorobenzyl)-2, 2-bis [(methoxymethoxy) methyl]-9-(morpholin-4-ylmethyl)- 7-thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, dd) N- [ (4-Chlorophenyl) methyl]-9'- (4-morpholinylmethyl)-4-oxo-7'- thioxospiro [cyclohexane-1,2' (3'H)- [7H] pyrido [1, 2,3-de] [1, 4] benzoxazine]-6'- carboxamide, ee) N- [ (4-Chlorophenyl) methyl]-4-hydroxy-9'- (4-morpholinylmethyl)-7'- thioxospiro [cyclohexane-1, 2' (3'H)-[7H]pyrido[1, 2,3-de] [1, 4] benzoxazine]-6'- carboxamide, ff) N- (4-Chlorobenzyl)-3, 9-bis (morpholin-4-ylmethyl)-7-thioxo-2, 3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, gg) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2-phenyl-2, 3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, hh) N- (4-Chlorobenzyl)-2, 2-difluoro-9- (morpholin-4-ylmethyl)-7-thioxo-2, 3-dihydro- 7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, ii) N- (4-Chlorobenzyl)-2- [ (methylsulfanyl) methyl]-9- (morpholin-4-ylmethyl)-7- thioxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, jj) N-(4-Chlorobenzyl)-2-[(dimethylamino)methyl]-9-(morpholin-4- ylmethyl)-7- thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, kk) N- (4-Chlorobenzyl)-2- [ (4-methyl-l-piperazinyl) methyl]-9- (morpholin-4-ylmethyl)- 7-thioxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, 11) Methyl ({ [6-{ [(4-chlorobenzyl) amino] carbonyl}-9-(morpholin-4-ylmethyl)-7- thioxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinolin-2-yl] methyl} thio) acetate, mm) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2- (1-pyrrolidinylmethyl)- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, nn) N- (4-Chlorobenzyl)-2- { [ (2, 3-dihydroxypropyl) sulfanyl] methyl}-9- (morpholin-4- ylmethyl)-7-thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3, 4-ij][quinoline-6-carboxamide,

oo) N-(4-Chlorobenzyl)-2-{[(2, 3-dihydroxypropyl) amino] methyl}-9- (morpholin-4- ylmethyl)-7-thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3, 4-ij]quinoline-6-carboxamide, pp) N-(4-Chlorobenzyl)-2-{[(2-hydroxymethyl)amino]methyl}-9-(mor pholin-4-ylmethyl)- 7-thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, qq) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2- (1-piperidinylmethyl)- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, rr) 2- { [bis (2-Hydroxyethyl) amino] methyl}-N- (4-chlorobenzyl)-9- (morpholin-4- ylmethyl)-7-thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, ss) N-(4-Chlorobenzyl)-9-(morpholin-4-ylmethyl)-7-thioxo-2-[[(2- pyridinylmethyl) amino] methyl}-2, 3-dihydro-7H- [ 1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide, tt) 2- [(8-{[6-{[(4-Chlorobenzyl) amino] carbonyl}-9-(morpholin-4-ylmethyl)-7-thioxo- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinolin-2-yl] methoxy}-8- oxooctanoyl) (methyl) amino] ethanesulfonic acid sodium salt, uu) [6-{[(4-Chlorobenzyl) amino] carbonyl}-9- (morpholin-4-ylmethyl)-7-thioxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinolin-2-yl] methyl dimethyl phosphate, vv) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2- { [ (4- pyridinylmethyl) amino] methyl}-2, 3-dihydro-7H- [ 1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide, ww) N- (4-Chlorobenzyl)-2- (lH-imidazol-1-ylmethyl)-9- (morpholin-4-ylmethyl)-7- thioxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, xx) N-(4-Chlorobenzyl)-2-{ [(4-chlorobenzyl) amino] methyl}-9-(morpholin-4-ylmethyl)- 7-thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, yy) N- (4-Chlorobenzyl)-3- (hydroxymethyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, zz) N- (4-Chlorobenzyl)-2- (4-hydroxyphenyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, aaa) N-(4-Chlorobenzyl)-2-{3-[(methoxymethoxy)methyl]phenyl}-9-(m orpholin-4- ylmethyl)-7-thioxo-2, 3-dihydro-7H-[1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, bbb) N- (4-Chlorobenzyl)-2- {2- [ (methoxymethoxy) methyl] phenyl}-9- (morpholin-4- ylmethyl)-7-thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, ccc) N- (4-Chlorobenzyl)-2- (2-hydroxyphenyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide,

ddd) N- [ (4-Chlorophenyl) methyl]-2,3,5,6-tetrahydro-9'- (4-morpholinylmethyl)-7'- thioxospiro [4H-pyran-4, 2' (3'H)- [7H] pyrido [1, 2,3-de] [1, 4] benzoxazine]-6'- carboxamide, eee) l, 1-Dimethylethyl 6-[[[(4-chylorophenyl) methyl] amino] carbonyl]-9'- (4- morpholinylmethyl)-7'-thioxospiro [piperidine-4,2' (3'H)-[7H]pyrido[1, 2,3-de] [1,4] benzoxazine]-1-carboxylate, fff) N-[(4-Chlorophenyl)methyl]-9'-(4-morpholinylmethyl)-7'-thiox ospiro [piperidine- 4,2' (3'H)- [7H] pyrido [1, 2,3-de] [1,4] benzoxazine]-6'-carboxamide, ggg) N- (4-Chlorobenzyl)-2, 2-bis (hydroxymethyl)-9- (morpholin-4-ylmethyl)-7-thioxo- 2, 3-dihydro-7H-[1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, hhh) N- [ (4-Chlorophenyl) methyl]-2', 3', 5', 6'-tetrahydro-9- (4-morpholinylmethyl)-7- thioxospiro [7H-pyrido[1, 2,3-de]-1,4-benzoxazine-2 (3H), 4'- [4H] thiopyran]-6- carboxamide, iii) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-3-phenyl-2, 3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, jjj) N- (4-Chlorobenzyl)-3, 3-bis (hydroxymethyl)-9- (3-hydroxy-l-propynyl)-7-thioxo- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, kkk) N- (4-Chlorobenzyl)-3, 3-bis (hydroxymethyl)-9- (3-hydroxypropyl)-7-thioxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, 111) N- (4-Chlorobenzyl)-2- [2- (methoxymethoxy) phenyl]-9- (morpholin-4-ylmethyl)-7- thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, mmm) N-(4-Chlorobenzyl)-2-{4-[(methoxymethoxy) methyl] phenyl}-9-(morpholin-4- ylmethyl)-7-thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide, nnn) 2- [2, 3-bis (Methoxymethoxy) phenyl]-N- (4-chlorobenzyl)-9- (morpholin-4-ylmethyl)- 7-thioxo-2,3-dihydro-7H- [1,4] oxazino [2, 3,4-ij] quinoline-6-carboxamide, ooo) N- [ (4-Chlorophenyl) methyl]-l-methyl-9'- (4-morpholinylmethyl)-7'- thioxospiro [piperidine-4, 2' (3'H)- [7H] pyrido [1,2,3-de] [1,4] benzoxazine]-6'- carboxamide, or a pharmaceutically acceptable salt.

Additional examples of the compounds of the present invention are: a) N- (4-Chlorobenzyl)-2- (hydroxymethyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxthioamide,

b) N- (4-Chlorobenzyl)-2- (R or S)- (hydroxymethyl)-9- (morpholin-4-ylmethyl)-7- thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxthioamide, <BR> <BR> <BR> c) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2-pyridin-3-yl-2, 3-dihydro- 7 H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxthioamide, d) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2-pyridin-4-yl-2, 3-dihydro- 7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxthioamide, e) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2-pyridin-2-yl-2, 3-dihydro- 7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxthioamide, N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2- (R or S)-pyridin-3-yl-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxthioamide, g) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-thioxo-2- (R or S)-pyridin-2-yl-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxthioamide, or a pharmaceutically acceptable salt.

Additional examples of the compounds of the present invention are: a) N- (4-Chlorobenzyl)-2- (hydroxymethyl)-9- (morpholin-4-ylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxthioamide, b) N- (4-Chlorobenzyl)-2- (R or S)- (hydroxymethyl)-9- (morpholin-4-ylmethyl)-7-oxo- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxthioamide, c) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2-pyridin-3-yl-2, 3-dihydro- 7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxthioamide, d) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2-pyridin-4-yl-2, 3-dihydro- 7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxthioamide, e) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2-pyridin-2-yl-2, 3-dihydro- 7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxthioamide, 0 N-(4-Chlorobenzyl)-9-(morpholin-4-ylmethyl)-7-oxo-2-(R or S)-pyridin-3-yl-2,3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxthioamide, g) N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2- (R or S)-pyridin-2-yl-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxthioamide, or a pharmaceutically acceptable salt.

The following Charts A-N describe the preparation of the compounds of formula I of the present invention. All of the starting materials are prepared by procedures described in these charts, by procedures well known to one of ordinary skill in organic chemistry or

can be obtained commercially. All of the final compounds of the present invention are prepared by procedures described in these charts or by procedures analogous thereto, which would be well known to one of ordinary skill in organic chemistry. All of the variables used in the charts are as defined below or as in the formula I above.

As shown in CHART A, acid A-1, which is 3-hydroxy-4-nitrobenzoic acid, is reacted with thionyl chloride to give the corresponding acid chloride, which is treated with morpholine to provide amide A-2. Reduction of the nitro group using hydrogen gas and palladium catalyst gives aminophenol A-3, which is alkylated using sodium hydride and diethyl chloromalonate in dimethylformamide to give lactam A-4. Simultaneous reduction of the three carbonyl groups using borane-methyl sulfide in tetrahydrofuran affords amine A-5. Treatment of the amine with diethyl ethoxymethylenemalonate provides A-6, which is derivatized to acetate A-7 using acetic anhydride and pyridine. Cyclization to A-8 is effected by phosphorus pentoxide in methanesulfonic acid. Treatment of A-8 with p- chlorobenzylamine at 150°C cleaves the acetate and aminolyzes the ester, giving amide A- 9. The alcohol is reacted with methanesulfonyl chloride and 2,4,6-collidine to give the intermediate mesylate A-10, which is subsequently reacted with a nucleophile of formula- RgRgNH, R8SH or R80H (wherein R8 and Rg are defined previously), or anions thereof, to provide compounds of formula A-11 wherein R6 is SOiR8, OR8, NR8R9, aryl, or het.

CHART A

As shown in CHART B, compound A-8, which is a racemic mixture, is resolved into its component enantiomers B-la and B-lb by preparative chiral HPLC. The individual isomers are carried forth separately through Formulae B-2 and B-3, according to the protocol described for Chart A.

CHART B

As shown in CHART C, alcohol of Formula A-9 is reacted with acetic anhydride to provide acetate C-1. Alternately, the alcohol can be coupled with a salt of suleptanic acid, which is 8- [Methyl (2-sulfoethyl) amino]-8-oxooctanoic acid, using diisopropylcarbodiimide to afford C-2. Alternately, C-9 can be reacted sequentially with phosphorus oxychoride and then methanol to provide phosphate C-3.

CHART C

As shown in CHART D, aminophenol of Formula A-3 is treated with methyl ot- bromophenylacetate and potassium carbonate in refluxing acetone to afford D-1. Reduction of the carbonyl groups using lithium aluminum hydride provides amine D-2, which is reacted with diethyl ethoxymethylenemalonate to furnish D-3. Cyclization to D-4 is effected with polyphosphoric acid, and aminolysis of the ester using p-chlorobenzylamine at 150 °C affords compound D-5.

CHART D

As shown in CHART E, aminophenol of Formula A-3 is treated with ethyl bromodifluoroacetate and sodium hydride in dimethylformamide to afford E-1. Reduction of the carbonyl groups using lithium aluminum hydride provides amine E-2, which is reacted with diethyl ethoxymethylenemalonate to furnish E-3. Cyclization to E-4 is effected with polyphosphoric acid, and aminolysis of the ester using p-chlorobenzylamine at 150 °C affords compound E-5.

CHART E As shown in CHART F, nitrophenol of Formula A-2 is alkylated using phenacyl bromide and tetrabutylammonium bisulfate as a phase transfer catalyst, giving compound F-1. Reduction of the nitro group with tin (IT) chloride is followed by spontaneous cyclization to enamine F-2. Reduction of the enamine with sodium borohydride furnishes F-3, which is further reduced using lithium aluminum hydride to afford amine F-4.

Reaction with diethyl ethoxymethylenemalonate provides F-5, which is cyclized using polyphosphoric acid to give F-6. Aminolysis of the ester using p-chlorobenzylamine at 150 °C affords compound F-7.

CHART F

As shown in CHART G, nitro ketone of Formula A-2 is reacted with epichlorohydrin in the presence of sodium hydroxide to give epoxide G-1. Reaction of the epoxide with morpholine in refluxing methanol provides amino alcohol G-2. The alcohol is oxidized with dimethyl sulfoxide and trifluoroacetic anhydride, and the resulting ketone is immediately hydrogenated using hydrogen gas and Raney nickel catalyst to give G-3.

Reduction of the remaining keto group is accomplished with lithium aluminum hydride, affording amine G-4. Treatment of the amine with diethyl ethoxymethylenemalonate, followed by polyphosphoric acid mediated cyclization of the intermediate enamine, provides compound G-5. Aminolysis of the ester using p-chlorobenzylamine at 150 °C provides compound G-6.

CHART G

As shown in CHART H, iodination of commercially available 2,3-difluorobenzoic acid H-1 using N-iodosuccinimide in trifluoromethanesulfonic acid provides trihalo-acid H- 2. The acid is reacted with carbonyldiimidazole to form the intermediate acyl imidazolide, which is treated with ethyl trimethylsilyl malonate and 1, 8-diazabicyclo [5.4.0] undec-7-ene to provide p-ketoester H-3. Compound H-3 is reacted with triethyl orthoformate and acetic acid, followed by tris (hydroxymethyl) methylamine to afford triol H-4. Cyclization is effected using potassium carbonate in DMF, giving tricycle H-5, and aminolysis using p- chlorobenzylamine at 150 °C affords H-6. The hydroxyl groups are masked as tert- butyldimethylsilyl ethers by reaction of the diol with tert-butyldimethylsilyl chloride and imidazole in dimethylformamide, giving H-7. Coupling of the iodide with propargyl alcohol using catalytic bis (triphenylphosphine) palladium (In dichloride and copper (1) iodide provides H-8. Removal of the silyl ethers using hydrochloric acid in ethanol affords compound H-9. Alternately, the triple bond in H-8 is reduced with hydrogen gas and catalytic platinum on carbon to afford H-10, which is desilylated using hydrochloric acid in ethanol to provide compound H-ll.

CHART H

As shown in CHART I, treatment of p-ketoester H-3 (Chart H) with triethyl orthoformate in refluxing acetic anhydride forms intermediate enol 1-1, which then reacts with amino alcohols I-7 to provide enamines 1-2. In Chart I, substitutent T refers to either a het or an aryl group. In some cases, groups T in Chart I may contain functional groups which are protected by suitable protective groups, such as methoxymethyl or tert- butyldimethylsilyl during the course of the synthesis. The protective groups are installed and then removed at the end of the synthesis using methods known to those skilled the art.

Cyclization of the enamines to tricycles I-3 is accomplished using cesium carbonate in DMF. Aminolysis of the ethyl ester using neat p-chlorobenzylamine affords amides 1-4.

The iodide is converted to the aldehyde I-5 using carbon monoxide and tri-n-butylstannane under palladium catalysis. Finally, reductive amination of the aldehyde provides 1-6.

Amino alcohols I-7 required for the sequence are prepared in two steps from the corresponding aldehydes I-8, by treatment of the aldehyde with trimethylsilyl cyanide and subsequent reduction of the TMS cyanohydrin with lithium aluminum hydride.

CHART I

CHART J illustrates a method for converting oxazinoquinolones to thioxazinoquinolones.

CHART J A morpholino substituted 7-thioxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline- 6-carboxamide, A-11, in a suitable solvent such as toluene and dichloroethane can be reacted with Lawesson's reagent in the presence of KHMDS. The mixture is then reacted at a suitable temperature range providing the desired thioketone J-1.

CHART K provides an alternative method to convert oxazinoquinolones to thioxazinoquinolones when they are substituted with one or more alkyl hydroxy groups.

For example, reacting compound H-ll in DMF with TIPSCl in the presence of imidiazole provides K-1 (See Wuts, P. G. Protecting Groups in Organic Chemistry 1999,123). Next, ketone K-1 is reacted with Lawesson's reagent in the presence of KHMDS in refluxing toluene and dichloroethane provides the thioketone K-2. The protected alcohol K-2 is then

treated with Bu4Nt in THF affording the hydroxyl compound K-3 (In Wuts, P. G.

Protecting Groups in Organic Chemistry 1999,124).

CHART K

CHART L illustrates a method for converting oxazinoquinolones to thioxazinoquinolone thioamides. A morpholino substituted 7-thioxo-2,3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide, A-ll, in a suitable solvent such as toluene and dichloroethane can be reacted with excess Lawesson's reagent. The mixture is then reacted at a suitable temperature range providing the desired thioketone L-1.

CHART L

As shown in CHART M, commercially available 2-fluoro-4-iodoaniline of Formula M-1 is reacted with diethyl ethoxymethylenemalnoate under thermal conditions to give the substituted 4-hydroxyquinoline of Formula M-2. Aminolysis of the ethyl ester using p- chlorobenzylamine under thermal conditions provides amide M-3. Palladium catalyzed formylation of the iodide affords aldehyde M-4, which is treated with morpholine and

sodium triacetoxyborohydride to furnish amine M-5. Compound M-5 is reacted with various epoxides M-7, using cesium carbonate or calcium ethoxide as base, to provide compounds M-8 or M-9. Where not commercially available, epoxides M-7 may be prepared by treatment of the corresponding carbonyl compounds M-6 with trimethylsulfonium methylsulfate and sodium hydroxide. Epoxides M-7 may also be prepared by other routes familiar to those skilled in the art; for example, by epoxidation of the corresponding olefins. If epoxides M-7 are prepared in optically enriched form, either by synthesis or resolution, the resulting products M-8 and M-9 will also be obtained in optically enriched form. This method for the preparation of the compounds of the present invention is further illustrated in the Preparation 46 and Examples 36-54.

CHART M In CHART N, hydroxyalkylbenzyl alcohols N-1 are protected with an appropriate blocking group, such as methoxymethyl or tert-butyldimethylsilyl, giving monoprotected alcohols N-2. Oxidation of the remaining hydroxyl group provides aldehydes N-3. Where hydroxyalkylbenzaldehydes N-4 are commercially available, they may be converted to compounds N-3 using similar protection chemistry. Addition of trimethylsilyl cyanide provides amino alcohols N-5, which are carried forth through the sequence N-6, N-7, N-8, N-9, and N-10 as described for Chart I. Finally, the protecting group is removed from compounds N-10 using standard conditions familiar to those proficient in the art, for example, by treatment with acid in ethanol, to give compounds N-11.

CHART N

It will be apparent to those skilled in the art that the described synthetic procedures are merely representative in nature and alternative synthetic processes are known to one of ordinary skill in organic chemistry.

The inventive compounds may be used in their native form or as salts. In cases where compounds are sufficiently basic or acidic to form stable nontoxic acid or base salts, administration of the compounds as salts may be appropriate. Examples of pharmaceutically acceptable salts are organic acid addition salts formed with acids which form a physiological acceptable anion, for example, tosylate, methanesulfonate, acetate, citrate, malonate, tartarate, succinate, benzoate, ascorbate, etoglutarate, and glycerophosphate. Suitable inorganic salts may also be formed, including hydrochloride, hydrobromide, sulfate, nitrate, bicarbonate, and carbonate salts.

Pharmaceutically acceptable salts may be obtained using standard procedures well known in the art, for example by reacting a sufficiently basic compound such as an amine with a suitable acid affording a physiologically acceptable anion. Alkali metal (for

example, sodium, potassium or lithium) or alkaline earth metal (for example calcium) salts of carboxylic acids can also be made.

"Pharmaceutically acceptable salts"refers to those salts which possess the biological effectiveness and properties of the parent compound and which are not biologically or otherwise undesirable.

Compounds of the present invention can conveniently be administered in a pharma- ceutical composition containing the compound in combination with a suitable excipient, the composition being useful in combating viral infections. Pharmaceutical compositions containing a compound appropriate for antiviral use are prepared by methods and contain excipients which are well known in the art. A generally recognized compendium of such methods and ingredients is Remington's Pharmaceutical Sciences by E. W. Martin (Mark Publ. Co., 15th Ed., 1975).

The compounds and compositions of the present invention can be administered parenterally (for example, by intravenous, intraperitoneal or intramuscular injection), topically, orally, or rectally, depending on whether the preparation is used to treat internal or external viral infections.

For oral therapeutic administration, the active compound may be combined with one or more excipients and used in the form of ingestible tablets, buccal tablets, troches, capsules, elixirs, suspensions, syrups, wafers, and the like. Such compositions and preparations should contain at least 0.1 % of active compound. The percentage of the compositions and preparations may, of course, be varied and may conveniently be between about 2 to about 60% of the weight of a given unit dosage form. The amount of active compound in such therapeutically useful compositions is such that an effective dosage level will be obtained.

The tablets, troches, pills, capsules, and the like may also contain the following: binders such as gum tragacanth, acacia, corn starch or gelatin; excipients such as dicalcium phosphate; a disintegrating agent such as corn starch, potato starch, alginic acid and the like; a lubricant such as magnesium stearate; and a sweetening agent such as sucrose, fructose, lactose or aspartame or a flavoring agent such as peppermint, oil of wintergreen, or cherry flavoring may be added. When the unit dosage form is a capsule, it may contain, in addition to materials of the above type, a liquid carrier, such as a vegetable oil or a polyethylene glycol. Various other materials may be present as coatings or to otherwise modify the physical form of the solid unit dosage form. For instance, tablets, pills, or

capsules may be coated with gelatin, wax, shellac or sugar and the like. A syrup or elixir may contain the active compound, sucrose or fructose as a sweetening agent, methyl and propylparabens as preservatives, a dye and flavoring such as cherry or orange flavor. Of course, any material used in preparing any unit dosage form should be pharmaceutically acceptable and substantially non-toxic in the amounts employed. In addition, the active compound may be incorporated into sustained-release preparations and devices.

The compounds or compositions can also be administered intravenously or intraperitoneally by infusion or injection. Solutions of the active compound or its salts can be prepared in water, optionally mixed with a nontoxic surfactant. Dispersions can also be prepared in glycerol, liquid polyethylene glycols, triacetin, and mixtures thereof and in oils.

Under ordinary conditions of storage and use, these preparations contain a preservative to prevent the growth of microorganisms.

Pharmaceutical dosage forms suitable for injection or infusion can include sterile aqueous solutions or dispersions or sterile powders comprising the active ingredient which are adapted for the extemporaneous preparation of sterile injectable or infusible solutions or dispersions, optionally encapsulated in liposomes. In all cases, the ultimate dosage form should be sterile, fluid and stable under the conditions of manufacture and storage. The liquid carrier or vehicle can be a solvent or liquid dispersion medium comprising, for example, water, ethanol, a polyol (for example, glycerol, propylene glycol, liquid polyethylene glycols, and the like), vegetable oils, nontoxic glyceryl esters, and suitable mixtures thereof. The proper fluidity can be maintained, for example, by the formation of liposomes, by the maintenance of the required particle size in the case of dispersions or by the use of surfactants. The prevention of the action of microorganisms can be brought about by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars, buffers or sodium chloride. Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminum monostearate and gelatin.

Sterile injectable solutions can be prepared by incorporating the active compound in the required amount in the appropriate solvent with various of the other ingredients enumerated above, as required, followed by filter sterilization. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum drying and the freeze drying techniques, which yield a powder of

the active ingredient plus any additional desired ingredient present in the previously sterile- filtered solutions.

For topical administration, the present compounds may be applied in pure form, i. e., when they are liquids. However, it will generally be desirable to administer them to the skin as compositions or formulations, in combination with a dermatologically acceptable carrier, which may be a solid or a liquid.

Useful solid carriers include finely divided solids such as talc, clay, microcrystalline cellulose, silica, alumina and the like. Useful liquid carriers include water, alcohols or glycols or water-alcohol/glycol blends, in which the present compounds can be dissolved or dispersed at effective levels, optionally with the aid of non-toxic surfactants. Adjuvants such as fragrances and additional antimicrobial agents can be added to optimize the properties for a given use. The resultant liquid compositions can be applied from absorbent pads, used to impregnate bandages and other dressings, or sprayed onto the affected area using pump-type or aerosol sprayers. Thickeners such as synthetic polymers, fatty acids, fatty acid salts and esters, fatty alcohols, modified celluloses or modified mineral materials can also be employed with liquid carriers to form spreadable pastes, gels, ointments, soaps, and the like, for application directly to the skin of the user.

Examples of useful dermatological compositions which can be used to deliver the compounds of formula I to the skin are known to the art; for example, see Jacquet et al.

(U. S. Pat. No. 4,608,392), Geria (U. S. Pat. No. 4,992,478), Smith et al. (U. S. Pat.

No. 4,559,157) and Wortzman (U. S. Pat. No. 4,820,508).

Useful dosages of the compounds of formula I can be determined by comparing their in vitro activity, and in vivo activity in animal models. Methods for the extrapolation of effective dosages in mice, and other animals, to humans are known to the art; for example, see U. S. Pat. No. 4,938,949.

The compound is conveniently administered in unit dosage form; for example, containing 5 to 1000 mg, conveniently 10 to 750 mg, most conveniently, 50 to 500 mg of active ingredient per unit dosage form. The desired dose may conveniently be presented in a single dose or as divided doses administered at appropriate intervals, for example, as two, three, four or more sub-doses per day. The sub-dose itself may be further divided, e. g., into a number of discrete loosely spaced administrations; such as multiple inhalations from an insufflator or by application of a plurality of drops into the eye.

For internal infections, the compositions can be administered orally or parenterally at dose levels, calculated as the free base, of about 0.1 to 300 mg/kg, preferably 1.0 to 30 mg/kg of mammal body weight, and can be used in man in a unit dosage form, administered one to four times daily in the amount of 1 to 1000 mg per unit dose.

For parenteral administration or for administration as drops, as for eye infections, the compounds are presented in aqueous solution in a concentration of from about 0.1 to about 10%, more preferably about 0.1 to about 7%. The solution may contain other ingredients, such as emulsifiers, antioxidants or buffers.

Generally, the concentration of the compound (s) of formula I in a liquid composition, such as a lotion, will be from about 0.1-25 wt-%, preferably from about 0.5-10 wt-%. The concentration in a semi-solid or solid composition such as a gel or a powder will be about 0.1-5 wt-%, preferably about 0.5-2.5 wt-%.

The exact regimen for administration of the compounds and compositions disclosed herein will necessarily be dependent upon the needs of the individual subject being treated, the type of treatment and, of course, the judgment of the attending practitioner.

The exact regimen for administration of the compounds and compositions disclosed herein will necessarily be dependent upon the needs of the individual subject being treated, the type of treatment and, of course, the judgment of the attending practitioner. The compounds of the present invention can be administered to an animal in need of treatment.

In most instances, this will be a human being, but the treatment of livestock and companion animals is also specifically contemplated as falling within the scope of the instant invention.

The antiviral activity of a compound of the invention can be determined using pharmacological models which are well known to the art, or using Test A described below.

The compounds of formula (I) and pharmaceutically acceptable salts thereof are useful as antiviral agents. Thus, they are useful to combat viral infections in animals, including man. The compounds are generally active against herpes viruses, and are particularly useful against the varicella zoster virus, the Epstein-Barr virus, the herpes simplex virus, the human herpes virus type 8 (HHV-8) and the cytomegalovirus (CMV).

While many of the compounds of the present invention have shown activity against the CMV polymerase, these compounds may be active against the cytomegalovirus by this or other mechanisms of action. Thus, the description below of these compounds'activity against the CMV polymerase is not meant to limit the present invention to a specific mechanism of action.

The HCMV polymerase assay is performed using a scintillation proximity assay (SPA) as described in several references, such as N. D. Cook, et al., Pharmaceutical Manufacturing International, pages 49-53 (1992); K. Takeuchi, Laboratory Practice, September issue (1992); US Patent No. 4,568,649 (1986); which are incorporated by reference herein. Reactions are performed in 96-well plates. The assay is conducted in 100 ul volume with 5.4 mM HEPES (pH 7.5), 11.7 mM KC1, 4.5 mM MgCl2, 0.36 mg/ml BSA, and 90 nM 3H-dTTP. Assays are run with and without CHAPS, (3- [ (3-Cholamidopropyl)- dimethylammonio]-l-propane-sulfonate) at a final concentration of 2 mM. HCMV polymerase is diluted in enzyme dilution buffer containing 50% glycerol, 250 mM NaCl, 10 mM HEPES (pH 7.5), 100 ug/ml BSA, and 0.01% sodium azide. The HCMV polymerase, which is expressed in recombinant baculovirus-infected SF-9 cells and purified according to literature procedures, is added at 10% (or 10 ul) of the final reaction volume, i. e., 100 plL Compounds are diluted in 50% DMSO and 10 p1 are added to each well. Control wells contain an equivalent concentration of DMSO. Unless noted otherwise, reactions are initiated via the addition of 6 nM biotinylated poly (dA)-oligo (dT) template/primer to reaction mixtures containing the enzyme, substrate, and compounds of interest. Plates are incubated in a 25 C or 37 C Ha0 bath and terminated via the addition of 40 pl/reaction of 0.5 M EDTA (pH 8) per well. Reactions are terminated within the time-frame during which substrate incorporation is linear and varied depending upon the enzyme and conditions used, i. e., 30 min. for HCMV polymerase. Ten ul of streptavidin-SPA beads (20 mg/ml in PBS/10% glycerol) are added following termination of the reaction. Plates are incubated 10 min. at 37 C, then equilibrated to room temperature, and counted on a Packard Topcount.

Linear regressions are performed and IC50s are calculated using computer software.

A modified version of the above HCMV polymerase assay is performed as described above, but with the following changes: Compounds are diluted in 100% DMSO until final dilution into assay buffer. In the previous assay, compounds are diluted in 50% DMSO. 4.5 mM dithiotherotol (DTT) is added to the polymerase buffer. Also, a different lot of CMV polymerase is used, which appears to be more active resulting in a more rapid polymerase reaction. Results of the testing of representative compounds of formula I in this assay are shown in Table 1 below.

Table 1. Biological Data B1, :, 1 , I'', e 4 : (Aw 10. 61 2 0. 76 w sM : 5 3 0. 76 4 1. 30 5 1. 10 6 0. 66 7 0. 67 8 1. 50 9 0. 59 10 0. 62 11 0. 54 12 0. 59 13 0. 59 14 0. 55 15 0. 42 16 0. 42 17 0. 27 18 0. 58 19 0. 57 20 0. 35 21 0. 67 22 0. 30 23 1. 10 24 0. 74 25 1. 30 26 0. 53 27 0. 92 28 0. 60 29 1. 00 30 0. 97 31 5. 00 32 3. 00 33 0. 52 34 0. 48 35 0. 61 36 0. 42 37 0. 38 38 0. 46 39 0. 33 40 0. 33 41 0. 44 42 0. 20 43 0. 40 44 1. 04 45 0. 41 46 0. 53 47 0. 83 48 2. 15 -polym. ea eic 49 2. 33 50 1. 17 51 0. 75 52 0. 81 53 0. 53 54 0. 60 55 0. 41 56 0. 66 57 0. 68 57 0. 32 58 0. 57 58 0. 27 59 0. 48 60 0. 46 61 0. 54 62 0. 38 63 0. 29 64 1. OS 65 0. 45 66 0. 59 67 1. 69 68 0. 82 69 0. 33

The symbol"--"refers to the data are not determined.

The compounds and their preparation of the present invention will be better understood in connection with the following Examples, which are intended as an illustration of and not a limitation upon the scope of the invention.

EXAMPLES Preparation 1: (3-Hydroxy-4-nitrophenyl) (4-morpholinyl) methanone (Formula A-2 of Chart A) To a stirred mixture of 55.0 g of 3-hydroxy-4-nitrobenzoic acid in 600 mL of dichloromethane is added 35 mL of thionyl chloride and 5.0 mL of DMF. The mixture is stirred and refluxed with exclusion of moisture for 1-2 h, when it suddenly becomes a clear solution. Refluxing is continued for another hour, then volatiles are removed under reduced pressure. The residual amber oil is dissolved in dichloromethane (200 mL), toluene (200 mL) is added, and the solution again concentrated under reduced pressure. The resulting amber oil is dissolved in 300 mL of dichloromethane, and to this solution, stirred and cooled to 0 °C, is added dropwise 65 mL of morpholine in 200 mL of dichloromethane.

The resulting mixture is stirred overnight, then washed with water containing sufficient 6N HC1 to render the aqueous phase acidic. The aqueous phase is extracted with one additional portion (100 mL) of dichloromethane, and the combined extracts dried (Na2S04) and concentrated under reduced pressure, affording an orange solid. Recrystallization from 1: 3 ethyl acetate in heptane provides 70. 34 g of the amide as a solid, mp 105.5-106.5 °C.

'H NMR (CDC13) 8 3.40,3.64,3.79,7.01,7.18,8.18,10.63 ppm HRMS (FAB) calcd for CnHNzOs +Hi 253.0824, found 253.0832.

Anal. Calcd for CllHl2N205 : C, 52.38, H, 4.80, N, 11.11, Found: C, 52.46; H, 4.85; N, 11.11.

Preparation 2: 2-Amino-5- (4-morpholinylcarbonyl) phenol (Formula A-3 of Chart A) A mixture of 15.36 g of the product of Preparation 1 and 1.25 g of 5% palladium on carbon in 450 mL of methanol is shaken under 30 psi of hydrogen gas for 3 h, then filtered through Celite. The solid is washed thoroughly with chloroform and methanol, and the combined filtrates concentrated under reduced pressure. The solid residue is suspended in ether, and the resulting solid filtered, washed with ether, and dried in vacuo to provide 13.34 g of the aminophenol as a solid.

'H NMR (DMSO-d6) 8 3.48,3.57,6.57,6.68,6.76,9.28 ppm.

Preparation 3: Ethyl 7- (4-morpholinylcarbonyl)-3-oxo-3, 4-dihydro-2H-1, 4- benzoxazine-2-carboxylate (Formula A-4 of Chart A) To a stirred, cooled (0 °C) mixture of 13.24 g the product of Preparation 2 in 60 mL of dry DMF, under argon, is added in portions 2.4 g of sodium hydride (60% dispersion in mineral oil). The mixture is stirred at 0 °C for 45 m, then 10.7 mL of diethyl chloromalonate is added, and the mixture allowed to warm to ambient temperature. After 18 h, the mixture is partitioned between dichloromethane and water containing sufficient dil. aq. HC1 to bring the pH of the aqueous phase to ca. 4. The aqueous phase is extracted with two additional portions of dichloromethane, and the combined extracts dried (MgS04) and concentrated under reduced pressure to a DMF solution of an intermediate amino ester.

This solution is heated at 80 °C under argon for 5 h, and the DMF is then distilled off under reduced pressure. Flash chromatography of the residue on silica using 3% methanol in dichloromethane affords 15.66 g of the title compound as a solid.

'H NMR (CDC13) 8 1.27,3.7,4.26,5.22,6.89,7.08,7.15,9.15.

Preparation 4: [7- (4-Morpholinylmethyl)-3, 4-dihydro-2H-1, 4-benzoxazin-2- yl] methanol (Formula A-5 of Chart A) To a stirred, cold (0 °C) solution of 15.59 g of the product of Preparation 3 in 90 mL of dry THF, under argon, is added 34 mL of borane-dimethyl sulfide complex. Following the addition, the ice bath is removed, whereupon the reaction warms spontaneously nearly to reflux. After the initial exothermic reaction, heat is supplied from an oil bath, and the temperature of the reaction maintained at 50 °C for 18 h. The solution is then cooled to 0 °C and quenched cautiously with methanol. Additional methanol (200 mL) is added, and the solution distilled through a Vigreux column at atmospheric pressure. Methanol is added at intervals until a total of 650 mL has distilled. Flash chromatography of the residual oil on silica using 5-6% methanol in dichloromethane provides 8.07 g of the title comopound as a solid.

1H NMR (CDC13) 8 2.4,3.3,3.70,3.8,4.34,6.56,6.72,6.80.

Preparation 5: Diethyl 2- { [2- (hydroxymethyl)-7- (4-morpholinylmethyl)-2, 3-dihydro- 4H-1, 4-benzoxazin-4-yl] methylene} malonate (Formula A-6 of Chart A) A mixture of 8.05 g of the product of Preparation 4 and 7.3 g of diethyl ethoxymethylenemalonate is heated at 130 °C under a slow stream of argon for 2 h, then

held under vacuum at 130 °C to remove volatile components. Flash chromatography of the residual amber oil on silica using 3% methanol in dichloromethane affords 11.51 g of the title compound as a solid.

'H NMR (CDC13) 8 1. 30, 1.33,2.43,3.42,3.58,3.71,3.82,4.19,4.24,4.28,6.9,8.01.

MS (ES+) m/z 435. 3.

Preparation 6: Diethyl 2-{[2-[(acetyloxy) methyl]-7-(4-morpholinylmethyl)-2, 3- dihydro-4H-1, 4-benzoxazin-4-yl] methylene} malonate (Formula A-7 of Chart A) A solution of 11.48 g of the product of Preparation 5,11 mL of pyridine, and 5.0 mL of acetic anhydride in 25 mL of dichloromethane is stirred at room temperature for 18 h, then concentrated under reduced pressure with toluene azeotrope to remove pyridine and acetic acid. Flash chromatography of the residual oil on silica using 2% methanol in dichloromethane provides 13.08 g of the title compound as a solid.

'H NMR (CDC13) 8 1.31,1.33,2.11,2.42,3.42,3.48,3.58,3.71,4.28,6.95,7.99.

TLC Rf 0. 35 (3% methanol in dichloromethane).

HRMS (FAB) calcd for C24H32N208 +Hl 477.2237, found 477.2236.

Preparation 7: Ethyl 2- [ (acetyloxy) methyl]-9- (4-morpholinylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxylate (Formula A-8 of Chart A) To 7.1 g of phosphorus pentoxide is added 50 mL of methanesulfonic acid, and the mixture is stirred under argon at 80-100 °C until a clear solution is obtained. The solution is cooled to 10 °C, and into this is cannulated a solution of 13.08 g of the product of Preparation 6 in 10 mL of dichloromethane. The resulting solution is stirred at 50 °C for 18 h, then cooled, diluted with dichloromethane (100 mL), and cautiously added to a stirred slurry of 72 g of sodium bicarbonate in 200 mL of water. Phases are separated and the aqueous extracted with four additional portions of dichloromethane, and the combined organic phases dried (Na2SO4) and concentrated under reduced pressure. Flash chromatography of the residue on silica gel using 3.5-4.5% methanol in dichloromethane affords 5.58 g of the title compound as a solid.

'H NMR (CDC13) 8 1.39,2.16,2.44,3.54,3.70,4.17,4.29,4.34,4.45,4.50,4.59,7.31, 7.91,8.28.

TLC Rf 0. 30 (5% methanol in dichloromethane).

MS (ES+) m/z 431. 2.

Example 1: N- (4-Chlorobenzyl)-2- (hydroxymethyl)-9- (4-morpholinylmethyl)-7-oxo- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula A-9 of Chart A)

A mixture of 5.17 g of the product of Preparation 7 and 10.2 g of p- chlorobenzylamine is stirred and heated at 145 °C under argon for 18 h, after which the bulk of excess amine is distilled off under reduced pressure. The residual solid is triturated well with ether, filtered and washed with ether, and dried under vacuum to provide 5.91 g of cream colored solid. This is triturated with boiling acetonitrile, filtered and washed with acetonitrile, and dried under vacuum to afford 5.76 g of the title compound as a solid.

'H NMR (DMSO-d6) 8 2.38,3.34,3.58,3.75,4.24,4.42,4.56,4.62,5.27,7.27,7.39,7.77, 8.75,10.43.

TLC Rf 0. 38 (10% methanol in dichloromethane) IR (mull) 1656,1611,1572,1556,1539,1504,1492,1417,1347,1286,1123,1112, 1105, 1090,806 cm''.

UV max 225 (32600,95% ethanol).

Preparation 8 : [6-1 [ (4-Chlorobenzyl) amino] carbonyl}-9- (4-morpholinylmethyl)-7-oxo- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinolin-2-yl] methyl methanesulfonate (Formula A-10 of Chart A) A solution of 726 mg of the product of Example 1 and 0.80 mL of 2,4,6-collidine is prepared with the aid of heat in 12 mL of DMF, and the solution is cooled to 10 °C for the addition of 0.35 mL of methanesulfonyl chloride. The mixture is allowed to warm to ambient temperature and stirred overnight, then partitioned between dichloromethane and water containing 25 mL of saturated aqueous NaHCO3. The aqueous phase is extracted with two additional portions of dichloromethane, and the combined organic phases dried (MgS04) and concentrated under high vacuum to remove DMF. Flash chromatography of the residue on silica gel using 3% methanol in dichloromethane provides 692 mg of the title compound as a solid.

'H NMR (CDC13 + CD30D) 8 2.45,3.14,3.57,3.70,4.26,4.41,4.57,7.28,7.38,7.94, 8.67,10. 36.

TLC Rf 0. 29 (5% methanol in dichloromethane).

MS (ES+) m/z 561.9.

Example 2: General procedure for mesylate displacement using nitrogen nucleophiles: N- (4-Chlorobenzyl)-2, 9-bis (4-morpholinylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula A-11 of Chart A) A solution of 91 mg of the product of Preparation 8 and 0.17 mL of morpholine in 1.0 mL of N-methylpyrrolidinone is heated at 80 °C for 6 h, then cooled and partitioned between water and dichloromethane or ethyl acetate. The aqueous phase is extracted with sufficient dichloromethane or ethyl acetate to remove product, and the organic phase is dried (MgS04). Volatiles are removed under high vacuum, and the residue purified by flash chromatography on silica using 2-5% methanol in dichloromethane to afford 45.2 mg of the title compound as a white solid. Further purification may be effected by recrystallization from acetonitrile or ethyl acetate-hexane.

Mp 178-180 °C. 1H NMR (CDC13) 8 2.46,2.60,2.72,2.86,3.59,3.77,4.18,4.37,4.47, 4.64,7.30,7.93,8.66,10.44.

TLC Rf 0. 22 (5% methanol in dichloromethane).

HRMS (FAB) calcd for C29H33CLN4O5 +H1 553.2217, found 553.2228.

Anal. Calcd for C29H33C1N405 : C, 62.98; H, 6.01; N, 10.13; Cl, 6.41; found: C, 62.85; H, 6.10; N, 9.97.

Example 3: N- (4-Chlorobenzyl)-2- [ (dimethylamino) methyl]-9- (4-morpholinylmethyl)- 7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula A-11 of Chart A)

Following the procedure in Example 2, the titled compound is obtained as a solid, mp 168-170 °C.

'H NMR (CDC13) S 2.35,2.45,2.64,2.77,3.57,3.70,4.13,4.35,4.44,4.63,7.30,7.37, 7.93,8.65,10.46.

TLC Rf 0. 47 (5% methanolic ammonia in dichloromethane).

HRMS (FAB) calcd for C27h31CLN4O4 +H1 511.2112, found 511. 2111.

Anal. Calcd for C27H31ClN404 : C, 63.46; H, 6.11; N, 10.96; Cl, 6.94; found: C, 63.22; H, 6.24; N, 10.63.

Example 4: N-(4-Chlorobenzyl)-2-[(4-methyl-1-piperazinyl)methyl]-9-(4- morpholinylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide (Formula A-11 of Chart A) Following the procedure in Example 2, the titled compound is obtained as a solid, mp 201-208 (d).

'H NMR (CDC13) b 2.33,2.4-2.7,2.72,2.86,3.57,3.70,4.15,4.36,4.48,4.64,7.29,7. 35, 7.92,8.65,10.46.

TLC Rf 0. 37 (7% methanolic ammonia in dichloromethane).

HRMS (FAB) calcd for C30H36CLN5O4 +Hl 566.2534, found 566.2547.

Anal. Calcd for C3oH36ClNs04 : C, 63.65; H, 6.41; N, 12.37; Cl, 6.26; found (av): C, 63.00; H, 6.37; N, 11.95.

Example 5 : N- (4-Chlorobenzyl)-9- (4-morpholinylmethyl)-7-oxo-2- (1- pyrrolidinylmethyl)-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula A-11 of Chart A)

Following the procedure in Example 2, the titled compound is obtained as a solid, mp 209.5-212.0 °C.

'H NMR (CDC13) 8 1.82,2.45,2.63,2.89,3.58,3.70,4.16,4.38,4.45,4.64,7. 30,7.37, 7.93,8.65,10.47.

TLC Rf 0. 31 (3% methanolic ammonia in dichloromethane).

IR (drift) 2960,2799,1655,1627,1608,1553,1501,1412,1348,1330,1319,1281, 1221, 1117, 808 cm-1 HRMS (FAB) calcd for C29H33CLN404 +Hl 537.2268, found 537.2259 Anal. Calcd for C29H33ClN404 : C, 64.86; H, 6.19; N, 10.43; Cl, 6.60; found: C, 64.89; H, 6.25; N, 10.38.

Example 6: N-(4-Chlorobenzyl)-2-{[(2, 3-dihydroxypropyl) amino] methyl}-9- (4- morpholinylmethyl)-7-oXo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide (Formula A-11 of Chart A) Following the procedure in Example 2, the titled compound is obtained.

'H NMR (CDC13 + CD30D) 8 2.47,2.79,3.53,3.65,3.74,4.15,4.39,4.63,7.30,7.37,7.92, 8.63,10.58.

TLC Rf0. 22 (12% methanolic ammonia in dichloromethane).

IR (drift) 1654,1626,1608,1555,1503,1414,1349,1330,1282,1223,1114,1094, 1014, 869,807 cm-1 HRMS (FAB) calcd for C28H33CLN406 +Hl 557.2167, found 557.2153 Anal. Calcd for C28H33ClN406 : C, 60.37; H, 5.97; N, 10.06; Cl, 6. 36 ; found (av): C, 59.87; H, 5.99; N, 9.94.

Example 7: N-(4-Chlorobenzyl)-2-{[(2-hydroxyethyl) amino] methyl}-9- (4- morpholinylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide (Formula A-11 of Chart A)

Following the procedure in Example 2, the titled compound is obtained.

'H NMR (CDC13 + CD30D) 8 2.47,2.85,3.07,3.60,3.71,4.24,4.45,4.63,7. 31,7.38,7.92, 8.63,10.59.

TLC Rf 0. 15 (6% methanolic ammonia in dichloromethane).

IR (drift) 1653,1626,1607,1580,1557,1502,1414,1348,1293,1281,1273,1224, 1116, 869, 807 cm-1 HRMS (FAB) calcd for C27H31CLN405 +Hl 527.2061, found 527.2067 Anal. Calcd for C27H31ClN4O5 : C, 61.53; H, 5.93; N, 10.63; Cl, 6.73; found (av): C, 61.15; H, 5.98; N, 10.64.

Example 8: N-(4-Chlorobenzyl)-9-(4-morpholinylmethyl)-7-oxo-2-(1-piperi dinylmethyl)- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula A-11 of Chart A) Following the procedure in Example 2, the titled compound is obtained as a solid, mp 213-215°C. 1H NMR (CDCl3) # 1,.46,1.60,2.5,2.63,2.81,3.57,3.70,4.13,4.39,4.46, 4.64,7.30,7.34,7.92,8.66,10.46.

TLC Rf0. 25 (5% methanol in dichloromethane).

IR (drift) 2931, 1653,1607,1572,1552,1500,1411,1349,1330,1284,1225,1113,1087, 810,800 cm-1 HRMS (FAB) calcd for C3oH3sCLN404 +Hl 551.2425, found 551.2435

Anal. Calcd for C30H35ClN4O4 : C, 65.39; H, 6.40; N, 10.17; Cl, 6.43; found: C, 65. 34 ; H, 6.46; N, 10.12.

Example 9: 2-{[bis (2-Hydroxyethyl) amino] methyl}-N-(4-chlorobenzyl)-9-(4- morpholinylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide (Formula A-11 of Chart A)

Following the procedure in Example 2, the titled compound is obtained. lH NMR (CDC13) 8 2.44,2.7,2.97,3.54,3.58,3.69,4.24,4.3,4.5,4.55,7.27,7.28,7.8 6, 8.59,10.51.

TLC Rf 0. 28 (10% methanol in dichloromethane).

IR (drift) 2953,2843,2810,1660,1608,1552,1500,1411,1355,1329,1284,1113, 1085, 808,799 cm~l HRMS (FAB) calcd for C29H35 CLN4O6 +H1 571.2323, found 571.2328 Anal. Calcd for C29H35C1N406 : C, 60.99; H, 6.18; N, 9.81; Cl, 6.21; found: C, 60.67; H, 6.24; N, 9.68.

Example 10: N-(4-Chlorobenzyl)-9-(4-morpholinylmethyl)-7y-oxo-2{[(2- pyridinylmethyl) amino] methyl}-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide (Formula A-11 of Chart A)

Following the procedure in Example 2, the titled compound is obtained.

'H NMR (CDC13) b 2.48,3.13,3.60,3.72,4.02,4.30,4.48,4.63,7.21,7.29,7.33,7.40, 7.68,7.93,8.58,8.64,10.44.

TLC Rf 0. 51 (7% methanolic ammonia in dichloromethane).

IR (drift) 1654,1626,1607,1554,1500,1453,1412,1348,1330,1282,1223,1113, 810, 801, 760 cm-1 HRMS (FAB) calcd for C3lH32CLN504 +Hl 574.2221, found 574.2233 Anal. Calcd for C3lH32ClN504 : C, 64.86; H, 5.62; N, 12.20; Cl, 6.18; found: C, 64.66; H, 5.62; N, 12.05.

Example 11: N-(4-Chlorobeznyl)-9-(4-morpholinylmethyl)-7-oxo-2-{[(3- pyridinylmethyl) amino] methyl}-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide (Formula A-11 of Chart A) Following the procedure in Example 2, the titled compound is obtained.

'H NMR (CDC13) 8 2.46,3.06,3.08,3.59,3.71,3.91,4.27,4.43,4.63,7.30,7.36,7.71, 7.93,8.54,8.60,8.64,10.44.

TLC Rf 0. 36 (6% methanolic ammonia in dichloromethane).

HRMS (FAB) calcd for C31H32CKLn5O4 +Hl 574.2221, found 574.2221 Anal. Calcd for C3lH32ClN504 : C, 64.86; H, 5.62; N, 12.20; Cl, 6.18; found: C, 64.65; H, 5.68; N, 12.07.

Example 12: N-(4-Chlorobenzyl)-9-(4-morphiolinylmethyl)-7-oxo-2-{[(4- pyridinylmethyl) amino] methyl}-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide (Formula A-11 of Chart A) Following the procedure in Example 2, the titled compound is obtained as a solid, mp 164-167 °C.

1H NMR (CDC13) 8 2.47,3.04,3.10,3.59,3.71,3.92,4.3,4.44,4.63,7.30,7.37,7.94,8 .57, 8.65,10.44.

TLC Rf0. 40 (6% methanolic ammonia in dichloromethane).

HRMS (FAB) calcd for C3lH32CLN504 +Hl 574.2221, found 574.2216 Anal. Calcd for C3iH32ClN504 : C, 64.86; H, 5.62; N, 12.20; Cl, 6.18; found: C, 64.17 ; H, 5.70; N, 12.07.

Example 13: N-(4-Chlorobenzyl)-2-(1H-imidazol-1-ylmethyl)-9-(4- morpholinylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2, 3,4-ij] quinoline-6- carboxamide (Formula A-11 of Chart A)

Following the procedure in Example 2, the titled compound is obtained as a solid, mp 217-219 °C (d).

'H NMR (CDCl3 + CD30D) 8 2.49,3.62,3.73,3.97,4.29,4.40,4.44,4.58,4.61,7.10,7.15, 7.30,7.42,7.72,7.94,8.59,10.44.

TLC Rf 0. 30 (5% methanol in dichloromethane).

IR (drift) 2916,2804,1656,1608,1570,1550,1500,1411,1347,1295,1280,1231, 1223, 1110, 800 cm-1 HRMS (FAB) calcd for C28H28CLN504 +Hl 534.1908, found 534.1907 Anal. Calcd for C28H28C1N504 : C, 62.98; H, 5.28; N, 13.11; Cl, 6.64; found: C, 62. 65; H, 5.30; N, 13.21.

Example 14: N-(4-Chlorobenzyl)-2-[(methylsulfanyl)methyl]-9-(4-morpholin ylmethyl)- 7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula A-11 of Chart A)

A mixture of 112 mg of the product of Preparation 8 and 112 mg of sodium methanethiolate in 0.5 mL of DMF is stirred at ambient temperature for 18 h, then partitioned

between water and chloroform. The aqueous layer is extracted with two additional portions of chloroform, and the combined organic phases dried (MgS04) and concentrated under reduced pressure. Flash chromatography of the residue on silica using 1-2% methanol in dichloromethane provides 72.5 mg of the title compound as a yellow solid. Recrystallization from acetonitrile gives a white solid, mp 190-191 °C.

'H NMR (CDC13) 8 2.26,2.46,2.83,3.01,3.58,3.70,4.21,4.48,4.64,7.29,7.36,7.94, 8.66,10.43.

TLC Rf 0. 45 (5% methanol in dichloromethane).

HRMS (FAB) calcd for C26H28CLN304S +Hl 514.1567, found 514.1568.

Anal. Calcd for C26H28C1N304S : C, 60.75; H, 5.49; N, 8.17; Cl, 6.90; S, 6.24; found: C, 60.60; H, 5.52; N, 8.12; Cl, 6.85; S, 6.15.

Example 15: 2-[(tert-Butylsulfonyl)methyl]-N-(4-chlorobenzyl)-9-(4- morpholinylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide (Formula A-11 of Chart A) Following the procedure in Example 14, the titled compound is obtained as a solid, mp 198-201 °C. 1H NMR (CDC13) 8 1.37,2.45,2.81,3.06,3.57,3.69,4.13,4.43,4.63, 7.29,7.35,7.92,8.64,10.42.

TLC Rf 0. 33 (3% methanol in dichloromethane).

HRMS (FAB) calcd for C29H34CLN304S +Hl 556.2037, found 556.2052 Anal. Calcd for C29H34CIN304S : C, 62.63; H, 6.16; N, 7.56; Cl, 6.38; S, 5.76; found: C, 62.46; H, 6.24; N, 7.50; Cl, 6.34; S, 5.74.

Example 16: N-(4-Chlorbenzyl)-2-{[(2-hydroxyethyl)sulfanyl]methyl}-9-(4- morpholinylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide (Formula A-11 of Chart A)

Following the procedure in Example 14, the titled compound is obtained.

'H NMR (CDC13 + CD30D) 8 2.48,2.85,2.93,3.04,3.60,3.72,3.80,4.24,4.55,4.63,7. 31, 7.38,7.92,8.63,10.51.

TLC Rf 0. 40 (10% methanol in dichloromethane).

IR (drift) 1651,1607,1578,1555,1500,1413,1347,1329,1281,1272,1232,1113, 1014, 869,807 cm-1 HRMS (FAB) calcd for C27H30CLN305S +Hl 544.1673, found 544.1672 Anal. Calcd for C27H3oClN305S : C, 59.60; H, 5.56; N, 7.72; Cl, 6.52; S, 5.89; found (av): C, 59.15; H, 5.55; N, 7.55.

Example 17: N-(4-Chlorobenzyl)-2-{[(1-methyl-1H-imidazol-2-yl)sulfanyl]m ethyl}-9-(4- morpholinylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide (Formula A-11 of Chart A) Following the procedure in Example 14, the titled compound is obtained as a solid, 'H NMR (CDC13) 8 2.45,3.39,3.55,3.56,3.63,3.69,4.27,4.50,4.63,4.72,6.92,6.95, 7.29,7.35,7.92,8.64,10.42.

TLC Rf 0. 22 (5% methanol in dichloromethane).

IR (drift) 1655,1626,1607,1578,1560,1499,1457,1414,1357,1347,1280,1273, 1117, 869,807 cm-1 HRMS (FAB) calcd for C29H30CLN5O4S +Hl 580.1785, found 580.1776 Anal. Calcd for C29H30ClN504S : C, 60. 04; H, 5.21; N, 12.07; Cl, 6.11; S, 5.53; found: C, 59.93; H, 5.15; N, 12.03. Example 18: Methyl ({[6-{[(4-chlorobenzyl) amino] carbonyl}-9- (4-morpholinylmethyl)-7- oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinolin-2-yl] methyl} sulfanyl) acetate (Formula A-11 of Chart A)

Following the procedure described in Example 14, the titled compound is obtained as a solid, mp 182.5-183.0 °C.

'H NMR (CDC13) 8 2.45,3.03,3.16,3.40,3.58,3.70,3.75,4.25,4.41,4.56,4.63,7.30, 7.36,7.94,8.66,10.42.

TLC Rf 0. 42 (5% methanol in dichloromethane).

IR (drift) 1735,1653,1607,1553,1501,1411,1352,1329,1281,1226,1141,1113, 1008, 810, 802 cm-1 HRMS (FAB) calcd for C28H30CLN306S +Hl 572.1622, found 572.1624 Anal. Calcd for C2gH30CIN306S : C, 58.79; H, 5.28; N, 7.34; Cl, 6.20; S, 5.60; found: C, 58.67; H, 5.26; N, 7. 33.

Example 19: N-(4-Chlorobenzyl)-2-{[(2, 3-dihydroxypropyl) sulfanyl] methyl}-9- (4- morpholinylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide (Formula A-11 of Chart A) Following the procedure described in Example 14, the titled compound is obtained.

'H NMR (CDCl3) 8 2.45,2.8,3.06,3.54,3.58,3.68,3.83,4.16,4.46,4.58,7.27,7.32,7 .90, 8.62,10.52.

TLC Rf 0. 32 (10% methanol in dichloromethane).

MS (ES+) m/z 574.4

Preparation 9: Ethyl 2- (R or S)- [ (acetyloxy) methyl]-9- (4-morpholinylmethyl)-7-oxo- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxylate (Formula B-1 of Chart B) Racemic acetate (3.2 g of the product of Preparation 7) is resolved using a 5x50 cm Chiralcel OD column at 30 °C with absolute ethanol as the mobile phase at a flow rate of 75 mL/min with UV detection at 326 nm. 1 g injections are made in 35 mL of 1: 4 CHCl3/EtOH. Following HPLC resolution, the compounds are purified by silica gel chromatography using 4% methanol in dichloromethane. Of the first eluting isomer, there is obtained 1.228 g; of the second peak, there is obtained 1.47 g. Analytical samples are prepared by recrystallization from ethyl acetate-hexane.

For Isomer 1: mp 142.5-144.0 °C.

'H NMR (CDC13) 8 1. 39,2.16,2.44,3.54,3.70,4.17,4.27,4.35,4.45,4.49,4.59,7.32, 7.91,8.29.

TLC Rf 0. 38 (8% methanol in dichloromethane).

IR (drift) 1745,1682,1637,1609,1556,1505,1324,1292,1273,1237,1222,1181, 1113, 879, 799 cni 1 HRMS (FAB) calcd for C22H26N207 +Hl 431.1818, found 431.1821 Anal. Calcd for C22H26N207 : C, 61.39 ; H, 6.09; N, 6.51; found: C, 61.24 ; H, 6.13; N, 6.49.

For Isomer 2: Mp 143.0-144.5 °C.

'H NMR (CDC13) 8 1.39,2.16,2.44,3.54,3.70,4.17,4.27,4.35,4.45,4.49,4.59,7.31, 7.91,8.28.

TLC Rf 0. 38 (8% methanol in dichloromethane).

IR (drift) 1745,1726,1682,1637,1609,1556,1505,1324,1291,1273,1237,1223, 1181, 1113, 799 cm-1 HRMS (FAB) calcd for C22H26N207 +Hl 431.1818, found 431.1831 Anal. Calcd for C22H26N207 : C, 61.39; H, 6.09; N, 6.51; found: C, 61.29; H, 6.12; N, 6.50.

Example 20: N- (4-Chlorobenzyl)-2- (R or S)- (hydroxymethyl)-9- (4-morpholinylmethyl)- 7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula B-2 of Chart B, isomer 1) 0 0 I I H i N CI O J o*J * Isomer1 OH

A mixture of 1.20 g of the product of Preparation 9 (isomer 1) and 2.4 g of p- chlorobenzylamine is heated under argon at 150 °C for 18 h, then excess amine is distilled off in vacuo. Flash chromatography of the residue on silica using 5-8% methanol in dichloromethane provides 1.27 g of the title amide as a tan solid. The solid is triturated well with ether, filtered, washed well with ether, and dried under vacuum to afford 1.22 g of the title compound as a solid.

'H NMR (CDC13 + CD30D) õ 2.49,3.62,3.73,3.95,4.4,4.64,7.31,7.40,7.91,8.65,10.63.

TLC Rf 0. 30 (10% methanol in dichloromethane).

Example 21: N- (4-Chlorobenzyl)-2- (R or S)- (hydroxymethyl)-9- (4-morpholinylmethyl)- 7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula B-2 of Chart B, isomer 2) 0 0 rl"-I I H N CI 0,,) *isomer2 OH According to the procedure described for isomer 1 in Example 20,1.41 g of the product of Preparation 9 (isomer 2) is converted to 1.43 g of the corresponding amide.

'H NMR (CDC13 + CD30D) 8 2.48,3.61,3.72,3.95,4.4,4.64,7.31,7.38,7., 8.64 (s, 1H), 10.62.

TLC Rf 0. 30 (10% methanol in dichloromethane).

Example 22: N- (4-chlorobenzyl)-9- (4-morpholinylmethyl)-7-oxo-2- (R or S)-{[(3- pyridinylmethyl) amino] methyl}-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide Isomer 1 (Formula B-3 of Chart B, where Rl=3-pyridinylmethyl, R2=H, and X=N) 0 0 I I H I N CI O J * LH I Isomer 1 N N

The compound is prepared using the procedures described in Preparation 8 and Example 2, using resolved isomer 1 of Example 20 and proceeding through the mesylate.

'H NMR (CDC13) § 2.45,3.05,3.09,3.57,3.70,3.91,4.27,4.43,4.63,7.29,7.35,7.70, 7.93,8.54,8.60,8.64,10.44.

TLC Rf 0. 40 (6% methanolic ammonia in dichloromethane).

MS (ES+) m/z 574.2.

Example 23: N- (4-Chlorobenzyl)-9- (4-morpholinylmethyl)-7-oxo-2- (R or S)-I [ (3- pyridinylmethyl) amino] methyl}-2,3-dihydro-7H- [1,4] oxazino [2,3, 4-ij]quinoline-6- carboxamide Isomer 2 (Formula B-3 of Chart B, where Rl=3-pyridinylmethyl, R2=H, and X=N) o o CN I H I N CI N J *Isomer 2 H N The compound is prepared using the procedures described in Preparation 8 and Example 2, using resolved isomer 2 of Example 21 and proceeding through the mesylate.

1H NMR (CDC13) 8 2.45,3.05,3.09,3.57,3.70,3.91,4.27,4.43,4.63,7.29,7.35,7.70, 7.93,8.54,8.60,8.64,10.44.

TLC Rf 0. 40 (6% methanolic ammonia in dichloromethane).

MS (ES+) m/z 574.3.

Example 24: [6-{[(4-Chlorobenzyl)amino]carbonyl}-9-(4-morpholinylmethyl) -7-oxo- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinolin-2-yl] methyl acetate (Formula C-1 of Chart C)

A mixture of 97 mg of the product of Example 1,0.19 mL of acetic anhydride, and 1 mL of chloroform is stirred for 18 h, then concentrated under reduced pressure with toluene azeotrope to remove acetic acid. Flash chromatography of the residue on silica using 2-3% methanol in dichloromethane provides 106.5 mg of the title compound as a white solid. An analytical sample is recrystallized from acetonitrile, giving white solid, mp 215-218 °C. tH NMR (CDC13) 8 2.16,2.46,3.59,3.71,4.22,4.33,4.4,4.56,4.63,7.30,7.40,7.95,8 .65, 10.41.

TLC Rf 0. 39 (5% methanol in dichloromethane).

IR (drift) 1745,1652,1626,1607,1558,1502,1413,1347,1280,1274,1223,1119, 1094, 1043,808 cni 1 HRMS (FAB) calcd for C27H28CLN306 +Hl 526.1744, found 526.1741 Anal. Calcd for C27H2sClN306 : C, 61.65; H, 5.36; N, 7.99; Cl, 6.74; found: C, 61.56; H, 5.44; N, 7.96.

Example 25: 2- [ (8-1 [6-1 [ (4-Chlorobenzyl) amino] carbonyl}-9- (4-morpholinylmethyl)-7- oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinolin-2-yl] methoxy}-8- oxooctanoyl) (methyl) amino] ethanesulfonic acid sodium salt (Formula C2 of Chart C) To a mixture of 97 mg of the product of Example 1 and 27 mg of DMAP in 0.5 mL of dry DMF is added 0.46 mL of a 0.65 M solution of suleptanic acid triethylammonium salt, which is 8- [methyl (2-sulfoethyl) amino]-8-oxooctanoic acid triethylammonium salt, in acetonitrile, followed by 38 uL of diisopropylcarbodiimide. After 5 days, volatile components are removed under vacuum, and the residue chromatographed on silica using 3- 6% methanolic ammonia in dichloromethane to afford the triethylammonium salt of the product. This is dissolved in n-butanol and chloroform, and the solution stirred with an

equal volume of saturated aqueous sodium sulfate solution. The aqueous phase is extracted with two additional portions of chloroform, and the combined organic phases filtered through anhydrous sodium sulfate and concentrated under reduced pressure to provide 92.5 mg of the title compound as a solid.

'H NMR (CDC13) 8 1. 3,1.6,2.4,3.1,3.6,3.7,4.2-4.7,7.3,7.9,8.68,10.45 ppm.

TLC Rf 0. 21 (10% methanol and 5% methanolic ammonia in dichloromethane).

MS (ES+) m/z 761.3.

MS (FAB) ? z/Z 761 (MH+), 97,95,85,83,81,69,67,55,43,23 HRMS (FAB) calcd for C36H45CLN4OIoS +Hl 761.2623, found 761.2643.

Example 26: [6- { [ (4-Chlorobenzyl) amino] carbonyl}-9- (4-morpholinylmethyl)-7-oxo- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinolin-2-yl] methyl dimethyl phosphate (Formula C-3 of Chart C) To a stirred mixture of 97 mg of the product of Example 1 in 1 mL of chloroform is added 0.19 rnL of phosphorus oxychloride. After the mixture is stirred for 18 h, 15 mL of methanol is added, and the solution is allowed to stand for 3 days. The solution is then concentrated under reduced pressure, and the residue partitioned between chloroform and aqueous NaHCO3. The aqueous phase is extracted with additional chloroform, and the combined organic phases are dried (Na2SO4) and concentrated under reduced pressure.

Flash chromatography of the residue on silica using 4% methanol in dichloromethane provides 56.0 mg of the title compound as a solid. in NMR (CDC13) 8 2.46,3.58,3.71,3.82,3.86,4.4,4.58,4.63,7.29,7.38,7.95,8.67, 10.38.

TLC Rf0. 25 (5% methanol in dichloromethane).

MS (ES+) m/z 592.2.

Preparation 10: 7- (4-Morpholinylcarbonyl)-2-phenyl-2H-1, 4-benzoxazin-3 (4H)-one (Formula D-1 of Chart D)

A mixture of 1.11 g of the product of Preparation 2,760 mg of potassium carbonate, and 0.86 mL of methyl a-bromophenylacetate in 10 mL of acetone is refluxed for 18 h, then cooled and partitioned between water and dichloromethane. The aqueous phase is extracted with additional dichloromethane, and the combined organic phases dried (Na2S04) and concentrated under reduced pressure. Flash chromatography of the residue on silica using 1.5-3% methanol in dichloromethane provides 1.27 g of the title compound as a solid.

'H NMR (CDC13) 8 3.68,5.70,6.85,7.01,7.09,7.33,7.43,9.82.

TLC Rf 0. 20 (3% methanol in dichloromethane).

MS (ES+) m/z 339.2 Preparation 11: 7- (4-Morpholinylmethyl)-2-phenyl-3, 4-dihydro-2H-1, 4-benzoxazine (Formula D-2 of Chart D) To a stirred, cooled (0 °C) solution of 1.27 g of the product of Preparation 10 in 15 mL of dry THF under argon is added in portions 290 mg of LAH. The mixture is allowed to warm to room temperature, stirred for 18 h, and then quenched with 0.29 mL of water, 0.29 mL of 3N NaOH, and 0.85 rnL of water. The mixture is filtered and the solid washed well with dichloromethane, and the filtrate is concentrated under reduced pressure. Flash chromatography of the residue on silica using 3% methanol in dichloromethane provides 1.00 g of the title compound as a slolid 'H NMR (CDC13) 8 2.43,3.32,3.37,3.46,3.69,3.92,5.05,6.60,6.75,6.89,7.4.

TLC Rf 0. 33 (5% methanol in dichloromethane).

Preparation 12: Diethyl 2-{[7-(4-morpholinylmethyl)-2-phenyl-2, 3-dihydro-4H-1, 4- benzoxazin-4-yl] methylene} malonate (Formula D-3 of Chart D) A mixture of 1.00 g of the product of Preparation 11 and 0.80 g of diethyl ethoxymethylenemalonate is heated under argon at 140 °C for 1 h, then under vacuum for 20 m. The mixture is cooled and chromatographed on silica gel using 2-3% methanol in dichloromethane to provide 1.32 g of the title compound as a solid.

'H NMR (CDC13) 8 1.19,1.31,2.46,3.46,3.56,3.64,3.72,4.16,4.25,5.05,6.97,7.04, 7.07,7.4,8.04.

TLC Rf 0. 38 (5% methanol in dichloromethane).

MS (ES+) m/z 481.3.

Preparation 13: Ethyl 9- (4-morpholinylmethyl)-7-oxo-2-phenyl-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxylate (Formula D-4 of Chart D) An intimate mixture of 1.32 g of the product of Preparation 12,7.0 g of polyphosphoric acid, and 4 mL of toluene is heated at 90 °C for 18 h, then transferred using a spatula to a stirred slurry of 8 g of NaHCO3 in 100 mL of water. The mixture is extracted with three portions of dichloromethane, and the combined organic phases dried (Na2S04) and concentrated under reduced pressure. Flash chromatography of the residue on silica using 3% methanol in dichloromethane affords 960 mg of the title compound as an orange solid. An analytical sample is recrystallized from acetonitrile, giving white solid, mp 213- 215 °C.

'H NMR (CDC13) b 1.40,2.47,3.59,3.70,4.24,4.30,4.37,5.31,7.4-7.5,7.98,8.31.

TLC Rf 0. 27 (5% methanol in dichloromethane).

HRMS (FAB) calcd for C25H26N2O5 +Hl 435.1920, found 435.1923 Anal. Calcd for C25H26N205 : C, 69. 11; H, 6.03; N, 6.45; found: C, 69.06; H, 6.13; N, 6.54.

Example 27: N- (4-Chlorobenzyl)-9- (4-morpholinylmethyl)-7-oxo-2-phenyl-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula D-5 of Chart D) A mixture of 219 mg of the product of Preparation 13 and 0.5 g of p- chlorobenzylamine is heated at 150 °C under nitrogen for 18 h, after which time excess amine is removed in vacuo. Flash chromatography of the residue on silica using 1.5-3% methanol in dichloromethane provides 251 mg of the title compound.

'H NMR (CDC13) 8 2.48,3.62,3.71,4.30,4.40,4.61,5.30,7.29,7.49,7.98,8.68,10.45 .

TLC Rf 0. 28 (3% methanol in dichloromethane).

MS (ES+) rn/z 530.3.

Preparation 14: 2,2-Difluoro-7- (4-morpholinylcarbonyl)-2H-1,4-benzoxazin-3 (4H)-one (Formula E-1 of Chart E)

To a cold (0 °C), stirred slurry of 1.11 g of the product of Preparation 2 in 5 mL of dry DMF under argon is added in portions 200 mg of sodium hydride (60% oil dispersion).

The mixture is stirred for 20 m at 0 °C, then 0.63 mL of ethyl bromodifluoroacetate is added dropwise. After 15 m, the mixture is allowed to warm to room temperature, and after 1 h is heated to 90 °C. After 3 h, the mixture is cooled and partitioned between ethyl acetate and water, and the aqueous phase is extracted with two additional portions of ethyl acetate. The combined organic phases are washed with water and brine, dried (MgS04), and concentrated under reduced pressure. Flash chromatography of the residue on silica using 2.5-3.5% methanol in dichloromethane affords 1.05 g of yellow solid. This is triturated well with 10 mL of 1: 1 ethyl acetate-hexane and the solid filtered, washed with 1: 1 ethyl acetate-hexane, and dried under vacuum to provide 824 mg of the title compound as an off-white solid. The solid is further purified by recrystallization from ethyl acetate- hexane, mp 214-217 °C.

1H NMR (CDC13 + CD30D) 8 3.74,7.09,7.22,7.25.

TLC Rf 0. 27 (5% methanol in dichloromethane).

IR (drift) 1739,1617,1586,1464,1433,1288,1265,1256,1228,1217,1117,1111, 1070, 824, 758 cm~l HRMS (FAB) calcd for Cl3Hl2F2N204 +Hl 299.0843, found 299.0836 Anal. Calcd for Cl3Hl2F2N204 : C, 52.35; H, 4.05; N, 9.39; found: C, 52.09; H, 4.07; N, 9.47.

Preparation 15: 2,2-Difluoro-7- (4-morpholinylmethyl)-3, 4-dihydro-2H-1,4- benzoxazine (Formula E-2 of Chart E) To a cold (0 °C), stirred solution of 805 mg of the product of Preparation 14 in 15 mL of dry THF, under argon, is added in portions 205 mg of LAH. The mixture is allowed to warm to room temperature and stirred overnight, then quenched cautiously with 0.2 mL of water, 0.2 mL of 3N NaOH, and 0.6 mL of water. Dichloromethane and Na2S04 are added, and the mixture is filtered and the solid washed with dichloromethane. The filtrate is concentrated under reduced pressure, and the residue chromatographed on silica using 2% methanol in dichloromethane to afford 423 mg of the title compound as a solid.

'H NMR (CDC13) 8 2.41,3.38,3.50,3.69,4.02,6.69,6.88,6.94.

TLC Rf 0. 34 (5% methanol in dichloromethane).

IR (drift) 3309,1526,1354,1320,1312,1266,1250,1216,1188,1108,999,964,88 5,856, 793 cm-1 HRMS (FAB) calcd for C13Hl6F2N202 +HI 271.1258, found 271.1264.

Preparation 16: Diethyl 2- { [2, 2-difluoro-7- (4-morpholinylmethyl)-2, 3-dihydro-4H-1, 4- benzoxazin-4-yl] methylene} malonate (Formula E-3 of Chart E) A mixture of 414 mg of the product of Preparation 15 and 870 mg of diethyl ethoxymethylenemalonate is heated under argon at 150 °C for 90 m, then cooled and chromatographed on silica using 2% methanol in dichloromethane to provide 739 mg of the title compound as a thick yellow oil.

1H NMNR (CDCl3) # 1.31,1.34,2.44,3.47,3.71,3.78,4.26,4.30,7.1,7.91.

TLC Rf 0. 31 (3% methanol in dichloromethane).

HRMS (FAB) calcd for C2lH26F2N206 +Hl 441.1837, found 441.1844.

Preparation 17: Ethyl 2,2-difluoro-9- (4-morpholinylmethyl)-7-oxo-2,3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxylate (Formula E-4 of Chart E) An intimate mixture of 675 mg of the product of Preparation 15 and 4.0 g of polyphosphoric acid is heated at 90 °C under argon, with occasional mechanical stirring, for 90 m, then cooled and added to a stirred slurry of 5 g of NaHCO3 in 50 mL of water. The mixture is extracted three times with dichloromethane, and the combined organic phases dried (MgS04) and concentrated under reduced pressure. Flash chromatography of the residue on silica using 2-3% methanol in dichloromethane provides 477 mg of the title compound. An analytical sample is recrystallized from ethyl acetate-hexane, giving the titled compound as crystals, mpl76-177 °C.

1H NMR (CDC13) § 1.37,2.45,3.58,3.71,4.32,4.56,7.46,8.02,8.35.

TLC Rf 0. 34 (5% methanol in dichloromethane).

IR (drift) 1678,1614,1560,1510,1325,1285,1261,1242,1228,1201,1191,1112, 943, 847,809 cm~l HRMS (FAB) calcd for CIsH20F2N205 +Hl 395.1418, found 395.1421.

Anal. Calcd for Cl9H2oF2N205 : C, 57.87; H, 5.11; N, 7.10; found: C, 57.67; H, 5.16; N, 7.10.

Example 28: N- (4-Chlorobenzyl)-2, 2-difluoro-9- (4-morpholinylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula E-5 of Chart 5)

A mixture of 118 mg of the product of Preparation 17 and 0.21 g of p- chlorobenzylamine is heated at 160 °C for 18 h, then placed under vacuum to remove excess amine. Chromatography of the residue on silica using 2-3% methanol in dichloromethane affords 135.8 mg of product as a yellow solid. Recrystallization from acetonitrile provides 111 mg of the title compound as white needles, mp 213.5-216.5 °C.

1H NMR (CDC13) b 2.46,3.61,3.72,4.57,4.63,7.29,7.54,8.08,8.76,10.26.

TLC Rf 0. 25 (3% methanol in dichloromethane).

IR (drift) 1658,1611,1582,1562,1508,1493,1327,1285,1258,1243,1229,1192, 1126, 1116,808cm' HRMS (FAB) calcd for C24H22CLF2N304 +Hl 490.1345, found 490.1343 Anal. Calcd for C24H22C1F2N304 : C, 58.84; H, 4.53; N, 8. 58; Cl, 7.24; found: C, 58.78; H, 4.56; N, 8.52.

Preparation 18: 2- [5- (4-Morpholinylcarbonyl)-2-nitrophenoxy]-1-phenylethanone (Formula F-1 of Chart F) A mixture of 1.01 g of the product of Preparation 1,800 mg of phenacyl bromide, 1.11 g of potassium carbonate, and 20 mg of tetrabutylammonium bisulfate in 4.0 mL of dichloromethane and 3 mL of water is stirred vigorously at room temperature for 18 h. The phases are then separated, and the aqueous phase extracted with one additional portion of dichloromethane. The combined organic phases are dried (Na2S04) and concentrated under reduced pressure. Flash chromatography of the residue on silica using 50% ethyl acetate in dichloromethane affords 1.465 g of the title compound as a white solid. An analytical sample is prepared by recrystallization from ethyl acetate-hexane, giving white crystals, mp 171.5-173 °C.

1H NMR (CDC13) 8 3.35,3.6,5.52,6.97,7.08,7.53,7.66,7.90,7.96.

TLC Rf 0. 30 (50% ethyl acetate in dichloromethane).

HRMS (FAB) calcd for Cl9Hl8N206 +HI 371.1243, found 371.1241

Anal. Calcd for ClgHl8N206 : C, 61.62; H, 4.90; N, 7.56; found: C, 61.52; H, 4.90; N, 7.51.

Preparation 19: 7- (4-morpholinylcarbonyl)-3-phenyl-2H-1, 4-benzoxazine (Formula F-2 of Chart F) To a solution of 3.13 g of stannous chloride dihydrate. in 12 mL of ethanol is added 1.026 g of the product of Preparation 18, and the mixture is stirred and heated at 60 °C for 30 m. Dilute aqueous NaOH is added in sufficient quantity to dissolve the precipitate which initially forms, and the mixture is extracted thrice with dichloromethane. The combined organic phases are dried (Na2S04) and concentrated under reduced pressure, and the residue chromatographed on silica using 50-75% ethyl acetate in dichloromethane to provide 622 mg of the title compound as a pale yellow crystalline solid. Recrystallization from ethyl acetate-hexane gives white needles, mp 175-177 °C.

1H NMR (CDC13) 8 3.7,5.09,6.98,7.05,7.5,7.94.

TLC Rf 0. 32 (50% ethyl acetate in dichloromethane).

IR 2856, 1633,1568,1458,1432,1280,1244,1114,1025,732,691 cm''.

HRMS (FAB) calcd for C9Hz8N203 +NAl 345.1215, found 345.1212 Anal. Calcd for Cl9Hl8N203 : C, 70.79; H, 5.63; N, 8.69; found: C, 70.63; H, 5.77; N, 8. 57.

Preparation 20: 7- (4-Morpholinylcarbonyl)-3-phenyl-3, 4-dihydro-2H-1, 4-benzoxazine (Formula F-3 of Chart F) A mixture of 586 mg of the product of Preparation 19 and 138 mg of sodium borohydride in 10 mL of ethanol is stirred at room temperature for 18 h, then added to 100 mL of stirred water. The-resulting solid is filtered, washed with water, and dried under vacuum to give 401 mg of white solid. The aqueous phases are extracted thrice with dichloromethane, and the combined organic phases dried (Na2S04) and concentrated under reduced pressure to provide an additional 203 mg of solid. The combined solids are chromatographed on silica using 50-75% ethyl acetate in dichloromethane to afford 510 mg of the title compound as a solid.

'H NMR (CDCl3) 8 3.68,3.98,4.30,4.52,6.66,6.93,6.94,7.4.

TLC Rf 0. 32 (50% ethyl acetate in dichloromethane).

IR 3306,2856,1612,1456,1430,1303,1284,1243,1114,1022,730,701 cm-1.

MS (ES+) m/z 325.2.

Preparation 21: 7- (4-Morpholinylmethyl)-3-phenyl-3, 4-dihydro-2H-1, 4-benzoxazine (Formula F-4 of Chart F) To a cold (0 °C), stirred solution of 576 mg of the product of Preparation 20 iii 5.0 mL of dry THF is added in portions 135 mg of LAH. The mixture is allowed to warm to room temperature and stirred for 3 h, then quenched cautiously with 0.16 mL of water, 0.16 mL of 3N NaOH, and 0.48 mL of water. Dichloromethane and NaSO4 are added, the mixture is filtered, and the solid washed with additional dichloromethane. The filtrates are concentrated under reduced pressure, and the residue flash chromatographed on silica using ethyl acetate and 3% methanol in ethyl acetate to afford 389 mg of white crystalline solid.

An analytical sample is recrystallized from ethyl acetate-hexane to give the title compound as white crystals, mp 135.5-136.5 °C.

1H NMR (CDC13) 8 2.44,3. 38,3.70,3.98,4.0,4.27,4.49,6.61,6.75,6.82,7.4.

TLC Rf 0. 28 (ethyl acetate).

IR 3348,2806,1516,1454,1292,1116,1006,701 cni 1.

HRMS (FAB) calcd for Cl9H22N202 +Hl 311.1759, found 311. 1761 Anal. Calcd for CigH22N2O2 : C, 73.52; H, 7.14; N, 9.02; found: C, 73.38; H, 7.19; N, 8.93.

Preparation 22: Diethyl 2-1 [7- (4-morpholinylmethyl)-3-phenyl-2, 3-dihydro-4H-l, 4- benzoxazin-4-yl] methylene} malonate (Formula F-5 of Chart F) A mixture of 378 mg of the product of Preparation 21 and 350 mg of diethyl ethoxymethylenemalonate is heated at 140 °C under argon for 2 h. Additional malonate (ca. 150 mg) is added, and the mixture heated at 120 °C for 18 h. Flash chromatography of the residue on silica using ethyl acetate provides 509 mg of the title compound as a solid.

1H NMR (CDC13) 8 0. 90, 1.26,2.42,3.43,3.70,3.9-4.2,4.32,4.50,5.27,6.83,6.99,7.1- 7.3,8.11.

IR 2980,2808,1708,1598,1509,1249,1219,1196,1117,1071 crri 1.

HRMS (FAB) calcd for C27H32N206 +Hl 481.2338, found 481.2344.

Preparation 23: Ethyl 9- (4-morpholinylmethyl)-7-oxo-3-phenyl-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxylate (Formula F-6 of Chart 6) An intimate mixture of 509 mg of the product of Preparation 22 and 2.4 g of polyphosphoric acid is heated at 90 °C, with occasional mechanical stirring, for 18 h. The resulting gum is added to a stirred slurry of 2.5 g of Na2HC03 in 50 mL of water, and the

mixture is extracted with three portions of dichloromethane. The combined organic phases are dried (MgSO4) and concentrated under reduced pressure. Flash chromatography of the residue on silica using 3-5% methanol in dichloromethane affords 375 mg of solid.

Recrystallization from acetonitrile-water provides 184 mg of white crystals, mp >190 °C.

'H NMR (CDC13) 8 1. 35, 2.47,3.59,3.71,4.33,4.56,5.30,7.15,7.33,7.4,8.03,8.23..

TLC Rf 0. 25 (5% methanol in dichloromethane).

IR 2809, 1723,1691,1608,1556,1500,1315,1226,1116,1073,808, 730 cm-1.

HRMS (FAB) calcd for C25H26N205 +Hi 435.1920, found 435.1920 Anal. Calcd for C25H26N205 : C, 69.11; H, 6.03; N, 6.45; found: C, 68.87; H, 6.19; N, 6.32.

Example 29: N- (4-Chlorobenzyl)-9- (4-morpholinylmethyl)-7-oxo-3-phenyl-2, 3- dihydro-7H- [1, 4loxazino [2,3,4-ij] quinoline-6-carboxamide (Formula F-7 of Chart F) A mixture of 103 mg of the product of Preparation 23 and 200 mg of p- chlorobenzylamine is heated at 150 °C for 18 h, then placed under vacuum to remove excess amine. Flash chromatography of the residue on silica using 2% methanol in dichloromethane affords 125. 3 mg of the title compound as a white solid. An analytical sample is recrystallized from toluene to give the title compound as white crystals.

1H NMR (CDC13) 8 2.48,3.61,3.72,4.58,4.59,5.37,7.13,7.28,7.40,8.02,8.59,10.44 .

TLC Rf 0. 28 (3% methanol in dichloromethane).

HRMS (FAB) calcd for C3oH28CLN304 +Hl 530.1846, found 530.1841 Anal. Calcd for C30H28ClN304 : C, 67.98; H, 5.32; N, 7.93; Cl, 6.69; found: C, 68.12; H, 5.38; N, 7.71.

Preparation 24: 5- (4-Morpholinylcarbonyl)-2-nitrophenyl 2-oxiranylmethyl ether (Formula G-1 of Chart G) A mixture of 504 mg of the product of Preparation 1 and 120 mg of powdered NaOH in 2 mL of epichlorohydrin is heated at 120 °C for 18 h, then cooled and partitioned between dil aqueous HC1 and ethyl acetate. The organic phase is washed with brine, dried (MgS04) and concentrated under reduced pressure. Flash chromatography of the residue on

silica using 2% methanol in dichloromethane provides 496 mg of the title compound.

Recrystallization from ethyl acetate-hexane gives the title compound as solid, mp 156.5- 158.0 °C.

'H NMR (CDC13) 8 2.85,2.93,3.39,3.7,4.13,4.49,7.06,7.21,7.87 TLC Rf 0. 47 (5% methanol in dichloromethane).

IR 2859, 1637,1607,1522,1437,1288,1240,1114,1016,842cm''.

HRMS (FAB) calcd for Cl4Hl6N206 +NAl 331.0906, found 331.0893 Anal. Calcd for C14Hl6N206 : C, 54.54; H, 5.23; N, 9.09; found: C, 54.16; H, 5.25; N, 8.92.

Preparation 25: 1- (4-Morpholinyl)-3- [5- (4-morpholinylcarbonyl)-2-nitrophenoxy]-2- propanol (Formula G-2 of Chart G) A solution of 442 mg of the product of Preparation 24 and 0.25 mL of morpholine in 2 mL of methanol is refluxed for 18 h, then concentrated under reduced pressure. Flash chromatography of the residue on silica using 2-5% methanol in dichloromethane provides 546 mg of the title compound as a solid.

'H NMR (CDC13) 8 2.6,3.41,3.7,4.15,4.23,7.05,7.21,7.89.

TLC Rf 0. 19 (5% methanol in dichloromethane).

IR 3425,2856,1637,1607,1523,1437,1288,1242,1115,1031,842 cni I.

MS (ES+) m/z 396.3.

Preparation 26: 7- (4-Morpholinylcarbonyl)-3- (4-morpholinylmethyl)-3, 4-dihydro-2H- 1,4-benzoxazine (Formula G-3 of Chart G) To a cold (-78 °C), stirred solution of 0.17 mL of DMSO in 2 mL of dichloromethane, under argon, is added dropwise 0.29 mL of trifluoroacetic anhydride. The solution is stirred 15 m, then a solution of 546 mg of the product of Preparation 25 in 1 mL of dichloromethane is added via cannula. The solution is warmed to-30 °C and stirred at that temperature for 30 m, then 0.96 mL of diisopropylethylamine is added. The solution is warmed to room temperature and partitioned between dichloromethane and water containing 2.0 mL of 1N HC1. The aqueous phase is extracted with two additional portions of dichloromethane, and the combined organic phases dried (Na2SO4), diluted with 40 mL of ethanol, and concentrated under reduced pressure to ca. 5 mL volume. To this solution is added Raney 2800 nickel catalyst, which is isolated from 3 mL of commercially available aqueous slurry by filtration and washing with ethanol with minimal exposure to air. The

mixture is shaken under 50 psi hydrogen gas for 18 h, then filtered through Celite with dichloromethane and methanol rinses. The filtrate is concentrated under reduced pressure, and the residue chromatographed on silica using 2-4% methanol in dichloromethane to provide 264 mg of the title compound as a white crystalline solid. Recrystallization from ethyl acetate in hexane gives the title compound as white crystals, mp 125-126 °C.

'H NMR (CDC13) 8 2.37,2.60,3.5-3.9,3.84,4.21,4.72,6.59,6.88.

TLC Rf 0.36 (5% methanol in dichloromethane).

HRMS (FAB) calcd for C18H25N304 +Hl 348.1923, found 348.1921 Anal. Calcd for C18H25N304 : C, 62.23; H, 7.25; N, 12.10; found: C, 62.21; H, 7.22; N, 11.97.

Preparation 27: 3,7-bis (4-Morpholinylmethyl)-3, 4-dihydro-2H-1, 4-benzoxazine (Formula G-4 of Chart G) To a cold (0 °C), stirred solution of 237 mg of the product of Preparation 26 in 2.0 mL of dry THF, under argon, is added 52 mg of LAH. The mixture is allowed to warm to room temperature and stirred for 30 m, then quenched cautiously with 50 pL of water, 50 pL of 3N NaOH, and 0.15 mL of water. Dichloromethane and Na2S04 are added, and the mixture filtered through Celite. The filtrate is concentrated under reduced pressure, and the residue flash chromatographed on silica using 2-6% methanol in dichloromethane to afford 211 mg of the title compound as a solid.

'H NMR (CDC13) 8 2.40,2.59,3.36,3.55,3.72,3.86,4.21,4.4,6.58,6.76.

TLC Rf 0. 31 (5% methanol in dichloromethane).

IR 3355,2808,1517,1290,1116,1005,865 crri'.

MS (ES+) m/z 334.3.

Preparation 28: Ethyl 3,9-bis (4-morpholinylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxylate (Formula G-5 of Chart G) A mixture of 211 mg of the product of Preparation 27 and 274 mg of diethyl ethoxymethylenemalonate is heated under argon at 140 °C for 2 h, then cooled and chromatographed on silica using 2-4% methanol in dichloromethane to provide 230 mg of the intermediate enamide, which is diethyl 2- { [3,7-bis (4-morpholinylmethyl)-2,3-dihydro- 4H-1, 4-benzoxazin-4-yl] methylene} malonate, as an orange foam. This is mixed thoroughly with 1.5 g of polyphosphoric acid, and the mixture is heated at 90 °C for 18 h, then cooled

and added to excess aqueous NaHCO3. The mixture is extracted thrice with dichloromethane, and the organic phases dried (Na2SO4) and concentrated under reduced pressure. Flash chromatography of the residue on silica using 2-5% methanol in dichloromethane affords 117 mg of the title compound.

'H NMR (CDC13) 8 1. 41,2.44,2.67,3.55,3.69,4.22,4.40,4.57,7.27,7.95,8. 37.

TLC Rf 0. 25 (5% methanol in dichloromethane).

IR 2811, 1722,1600,1555,1502,1319,1292,1227,1116,912,867,731 cm-1.

MS (ES+) m/z 458.3.

Example 30: N- (4-Chlorobenzyl)-3, 9-bis (4-morpholinylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula G-6 of Chart G) A mixture of 117 mg of the product of Preparation 28 and 0.20 g of p- chlorobenzylamine is heated at 150 °C for 18 h, then excess amine is removed under vacuum. Flash chromatography of the residue on silica using 2-4% methanol in dichloromethane affords 11.6 mg of the title compound.

'H NMR (CDC13) 8 2.41,2.63,2.77,3.57,3.69,4.31,4.66,7.30,7.33,7.96,8.68 (s, 1H), 10.46.

TLC Rf 0. 31 (5% methanol in dichloromethane).

IR 2812, 1658,1608,1551,1500,1286,1116,867,809,730 clip.

HRMS (FAB) calcd for Ca9H33CLN4O5-I-Hl 553.2217, found 553.2213.

Preparation 29: 2,3-Difluoro-5-iodobenzoic acid (Formula H-2 of Chart H) To a cold (0 °C), stirred solution of 4.74 g of 2, 3-difluorobenzoic acid in 15.0 mL of trifluoromethanesulfonic acid is added in portions 8.1 g of powdered N-iodosuccinimide.

Following the addition, the mixture is allowed to warm to room temperature, stirred for 5 h, then poured onto 200 mL of cracked ice containing 5 g of sodium bisulfite. The mixture is stirred well for 15 m, then filtered, and the solid washed well with water and dried under vacuum to provide 6.78 g of the title compound as a solid.

'H NMR (CDC13) 8 7.81,8.09.

IR 3082, 1713,1473,1280 caf'.

MS (ES-) n>/z 282.8.

Preparation 30 : Ethyl 3- (2, 3-difluoro-5-iodophenyl)-3-oxopropanoate (Formula H-3 of Chart H) To a stirred solution of 2.02 g of the product of Preparation 29 in 10 mL of dry THF, under argon, is added 1.42 g of carbonyldiimidazole and 20 mg of DMAP. In a separate flask, 1.49 g of ethyl potassium malonate is suspended in 10 mL of CH3CN at 0 °C under argon, and to the slurry is added 1.0 mL of chlorotrimethylsilane. The mixture is stirred at ambient temperature for 18 h, then re-cooled to 0 °C. To the mixture is added 2.3 mL of DBU, and after 30 min the acyl imidazolide solution prepared above is added via cannula.

The mixture is stirred for 4 h at room temperature, then partitioned between ether and excess dilute HCI. The aqueous phase is back extracted with one additional portion of ether, and the combined organic phases washed with 0.1 N HC1 and brine, dried (MgS04), and concentrated under reduced pressure. Flash chromatography of the residue on silica using 5% EtOAc in heptane provides 2.13 g of the title compound as a white solid.

'NMR (CDC13) S 1.34,4.26,5.81,7.57,7.95.

TLC Rf 0. 44 (10% EtOAc in hexane).

IR 1622,1490,1420,1213,1036, 958,800 cm-1.

MS (ES-) m/z 352.9.

Preparation 31: Ethyl (2-E and Z)-2-(2, 3-difluoro-5-iodobenzoyl)-3-{[2-hydroxy-1, 1- bis (hydroxymethyl) ethyl] amino}-2-propenoate (Formula H-4 of Chart H) A solution of 2.12 g of the product of Preparation 30 and 1.5 mL of triethyl orthoformate in 6 mL of acetic anhydride is refluxed under nitrogen for 2 h, then concentrated under reduced pressure to a viscous oil. This is dissolved in 6 mL of ethanol, and 1.45 g of tris (hydroxymethyl) aminomethane is added. The solution is stirred at room temperature for 18 h, then concentrated under reduced pressure. Flash chromatography of the residue on silica using 5-7% methanol in dichloromethane affords 2.77 g of the title compound as a tan foam.

'NMR (CDC13) (E/Z mixture of isomers) 8 0.87,0.93,3.78,3.98,4.23,7.35,7.49,8.46, 10.09,11.33.

TLC Rf 0. 32 (10% methanol in dichloromethane).

IR 3400, 1670,1622,1481,1430,1323,1296,1274,1256,1222,1056,912,733 cm-1.

HRMS (FAB) calcd for Cl6Hl8F2INO6 +Hl 486.0227, found 486.0240.

Preparation 32: Ethyl 3,3-bis (hydroxymethyl)-9-iodo-7-oxo-2,3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxylate (Formula H-5 of Chart H) A mixture of 2.77 g of the product of Preparation 31 and 1. 74 g of potassium carbonate in 20 mL of DMF is heated at 130 °C under argon for 2 days, after which DMF is distilled off under reduced pressure. To the brown residue is added water, and the mixture is stirred for 20 m then filtered. The solid is washed with water, ethyl acetate, and ether, and dried under vacuum to provide 1.76 g of the title compound as a solid.

'NMR (CDC13 + TFA) 81. 48,4.24,4.42,4.60,4.63,8.03,8.62,9.49.

HRMS (FAB) calcd for Cl6Hl6INO6 +Hl 446.0102, found 446.0100.

Preparation 33: N- (4-Chlorobenzyl)-3, 3-bis (hydroxymethyl)-9-iodo-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula H-6 of Chart H) A mixture of 1.69 g of the product of Preparation 32 and 3.2 g of p- chlorobenzylamine is heated under argon at 160 °C for 18 h, then cooled and triturated with dichloromethane. The resulting solid is filtered, washed with dichloromethane, and dried under vacuum to provide 1.50 g of the title compound as a solid.

1NMR (CDC13 + TFA) 8 4.12,4.35,4.56,4.64,7.3,7.91,8.54,9.25,9.4.

MS (ES+) m/z 541.0.

Preparation 34: 3,3-bis (f [tert-Butyl (dimethyl) silyl] oxy} methyl)-N- (4-chlorobenzyl)-9- iodo-7-oxo-2,3-dihydro-7H- [1,4] oxazino [2, 3,4-ij] quinoline-6-carboxamide (Formula H- 7 of Chart H) A mixture of 1.49 g of the product of Preparation 33,661 mg of imidazole, and 1.25 g of tert-butyldimethylsilyl chloride in 6 mL of DMF is stirred at room temperature for 18 h, then partitioned between ethyl acetate and aqueous NaHCO3. The organic phase is washed with water and brine, dried (Na2SO4), and concentrated under reduced pressure.

Flash chromatography of the residue on silica using 20% ethyl acetate in heptane affords 1.72 g of the title compound as a white solid. An analytical sample is recrystallized from methanol to give the title compound as a solid, mp 157.5-159.0 °C.

'NMR (CDC13) 8 0.00 (used as reference peak), 0.03,0.82,3.94,4.02,4.37,4.92,7.26, 7.53,8. 39,8.81,10.27.

TLC Rf 0. 38 (20% ethyl acetate in hexane).

IR (drift) 2953,2930,2856,1670,1572,1543,1483,1467,1252,1122,1088,841,8 37, 800, 776 cm-1 HRMS (FAB) calcd for C33H46CLIN205Si2 +Hl 769.1758, found 769.1748 Anal. Calcd for C33H46ClE205Si2 : C, 51.52; H, 6.03; N, 3.64; Cl, 4.61; found (av): C, 51.14; H, 6.06; N, 3.59.

Preparation 35: 3,3-bis (Iftert-Butyl (dimethyl) silyl] oxy} methyl)-N-(4-chlorobenzyl)-9- (3-hydroxy-1-propynyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3, 4-ij]quinoline-6- carboxamide (Formula H-8 of Chart H) To a mixture of 385 mg of the product of Preparation 34,70 mg of copper (I) iodide, and 18 mg of bis (triphenylphosphine) palladium (II) dichloride is added 40 pL of propargyl alcohol in 4 mL of diethylamine. The mixture is stirred overnight at room temperature, becoming a clear red solution. Volatile components are removed under reduced pressure and the residue flash chromatographed on silica using 10-15% ethyl acetate in dichloromethane to provide 333 mg of the title compound as a solid.

'NMR (CDC13) 8 0.00 (used as reference peak), 0.03,0.82,4.02,4.38,4.43,4.63,7.02,7.3, 7.78,8.73,10.34.

TLC Rf 0. 35 (10% ethyl acetate in dichloromethane).

MS (ES+) m/z 697.3.

Example 31: N- (4-Chlorobenzyl)-3, 3-bis (hydroxymethyl)-9- (3-hydroxy-l-propynyl)-7- oxo-2,3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula H-9 of Chart H) A mixture of 52 mg of the product of Preparation 35,0.5 mL of concentrated hydrochloric acid, and 1 mL of ethanol is stirred at room temperature for 3 days, then added to 10 mL of rapidly stirred water. The resulting solid is filtered, washed with water, and

dried under vacuum to provide 34 mg of buff solid. Chromatography of this material on silica using 5-10% methanol in dichloromethane affords 29.4 mg of the title compound as a solid.

'NMR (CDC13 +CD30D) 8 3.88,4.09,4.45,4.63,7.28,7. 31,8.03,8.92.

TLC Rf 0. 38 (10% methanol in dichloromethane).

MS (ES+) m/z 469.0.

Preparation 36: 3,3-bis ({[tert-Butyl (dimethyl) silyl] oxy} methyl)-N- (4-chlorobenzyl)-9- (3-hydroxypropyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide (Formula H-10 of Chart H) A mixture of 175 mg of the product of Preparation 35 and 70 mg of 5% platinum on carbon in 6 mL of ethyl acetate is shaken under 40 psi H2 for 5 h, then filtered through Celite. The filtrate is concentrated under reduced pressure and the residue chromatographed on silica using 30% ethyl acetate in dichloromethane to provide 142 mg of the title compound as a pale yellow solid. An analytical sample is recrystallized from ethanol to give the title compound as white needles.

Physical properties are as follows: 1NMR (CDC13) 8 0.00 (used as reference peak), 0.03,0.83,1.94,2.82,3.68,3.97,4.02, 4.37,4.63,7.11,7.3,7.90,8.80,10.43.

TLC Rf 0. 32 (30% ethyl acetate in dichloromethane).

IR (drift) 2951,2930,2858,1662,1604,1572,1554,1491,1253,1115,1092,1064, 840, 802, 780 cm' HRMS (FAB) calcd for C36H53CLN206Si2 +Hl 701.3209, found 701.3202 Anal. Calcd for C36H53ClN206Si2 : C, 61.64; H, 7.61; N, 3.99; Cl, 5.05; found: C, 61.35; H, 7.74; N, 3.97.

Example 32: N- (4-Chlorobenzyl)-3, 3-bis (hydroxymethyl)-9- (3-hydroxypropyl)-7-oxo- 2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula H-11 of Chart H)

A solution of 132 mg of the product of Preparation 36 in 2.0 mL of ethanol and 1.0 mL of concentrated hydrochloric acid is stirred at room temperature for 18 h, then concentrated under reduced pressure. Flash chromatography of the residue on silica using 5-8% methanol in dichloromethane provides 85.3 mg of the title compound as a white solid. An analytical sample is recrystallized from methanol to give the title compound as white crystals, mp 173.0-174.5 °C.

1NMR (CDC13 + CD30D) 8 1.90,2.81,3.61,3.88,4.10,4.43,4.64,7.16,7.31,7.84,8.90.

TLC Rf 0. 35 (10% methanol in dichloromethane).

IR (drift) 3363,1654,1628,1605,1552,1492,1367,1348,1338,1301,1291,1266, 1090, 1061,801 cm~l HRMS (FAB) calcd for C24H25CLN206 +Hl 473.1479, found 473.1471 Anal. Calcd for C24H25C1N206 : C, 60.95; H, 5.33; N, 5.92; Cl, 7.50; found: C, 59.00; H, 5.63; N, 5.70.

Preparation 37: 2-Amino-1-(2-pyridinyl) ethanol (I-7 of Chart I, T=2-pyridyl) To 2.68 g of 2-pyridylcarboxaldehyde, stirred under argon at 0 °C, is added 3.7 mL of trimethylsilyl cyanide. After 10 min the ice bath is removed and the yellow liquid stirred for 30 min at ambient temperature. The resulting TMS cyanohydrin is dissolved in 10 mL of dry ether. In a three-necked flask fitted with argon inlet and overhead mechanical stirrer is placed 1.05 g of LAH and 50 mL of dry ether. The slurry is cooled to 0 °C under argon and stirred vigorously while the cyanohydrin solution is added dropwise via cannula.

Following the addition, the reaction is stirred at room temperature for 2 h, then recooled to 0 °C and cautiously quenched with 1.0 mL of water (dissolved in 10 mL of THF), 1.0 mL of 3NNaOH, and 3. 0 mL of water, added sequentially. CH2Cl2 (30 mL) and Na2S04 are added, and the mixture is well stirred for 30 min and then filtered. The filter cake is washed well with 1: 1 CH2Cl2 : ether, and the combined filtrates concentrated under reduced pressure to provide 5.02 g of crude title compound as a deep red oil. The crude material is used directly in the subsequent reaction.

'H NMR (CDC13) 8 2.87,3.12,4.71,7.20,7.35,7.69,8.55.

Preparation 38: Ethyl 2-(2, 3-difluoro-5-iodobenzoyl)-3-{[2-hydroxy-2-(2- pyridinyl) ethyl] amino}-2-propenoate (I-2 of Chart I, T=2-pyridyl)

A solution of 1.79 g of ß-ketoester H-3 of Preparation 30 and 1. 3 mL of triethyl orthoformate in 5 mL of acetic anhydride is refluxed for 2 h, then concentrated under reduced pressure. The residual oil is stirred at 70 °C under 0.1 mmHg for 20 min to remove volatile components, providing the crude enol ether. This is dissolved in 2 mL of ethanol, and a solution of approximately 25 mmol of amino alcohol I-7 of Preparation 37 in 10 mL of ethanol is added. The resulting deep red solution is stirred at room temperature for 15 h, then concentrated under reduced pressure. The residual oil is partitioned between EtOAc and water, and the organic phase is washed with two additional portions of water, once with brine, dried (MgS04), and concentrated under reduced pressure. Flash chromatography of the crude material on silica using EtOAc provides 2.14 g of the title compound as an orange gum. The NMR spectrum is complex due to E/Z isomerism.

TLC Rf 0. 36 (EtOAc).

Preparation of 39: Ethyl 9-iodo-7-oxo-2- (2-pyridinyl)-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxylate (I-3 of Chart I, T=2-pyridyl) A stirred mixture of 2.13 g of I-2 of Preparation 38 and 3.04 g of cesium carbonate in 8 mL of DMF is heated at 100 °C under argon for 18 h, then cooled and diluted with 100 mL of water. The resulting solid is filtered, washed well with water, and dried under vacuum. Flash chromatography of the solid on silica using 3% MeOH in CH2C12 affords 2.06 g of the title compound as a peach-colored solid. A sample recrystallized from acetonitrile provides white crystals, mp 224-225 °C.

'NMR (CDC13) 8 1.38,4.34,4.53,4.64,5.54,7.33,7.62,7.64,7.81,8.27,8.30,8.61.

TLC Rf 0. 45 (5% MeOH in CH2C12.) IR 1682, 1637,1611,1589,1550,1491,1399,1367,1316,1267,1248,1235,1183, 800, 770 cm~l OAMS supporting ions at: ESI+ 463.0 HRMS (FAB) 463.0150 Anal. found: C, 49.36; H, 3.30; N, 6.09.

Preparation 40: N- (4-Chlorobenzyl)-9-iodo-7-oxo-2- (2-pyridinyl)-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (I-4 of Chart I, T=2-pyridyl) A mixture of 1.86 g of I-3 of Preparation 39 and 3.5 g of p-chlorobenzylamine is stirred and heated at 150 °C. After 18 h, excess amine is distilled off under vacuum, and

the residue is adsorbed onto silica gel and flash chromatographed on silica using 1-3% MeOH in CH2C12 to provide 1.69 g of the amide as a pale yellow solid.

'NMR (CDC13+CD30D) 84. 61,4.62,4.76,5.55,7.30,7.38,7.62,7.73,7.85,8. 38,8.66, 8.71.

TLC Rf 0. 37 (2% MeOH in CH2C12) OAMS supporting ions at: ESI+ 558. 0.

Preparation 41: N- (4-Chlorobenzyl)-9-formyl-7-oxo-2- (2-pyridinyl)-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (I-5 Chart I, T=2-pyridyl) In a dry 50 mL recovery flask fitted with a Liebig condenser topped with a rubber septum is placed 520 mg of iodide I-4 of Preparation 40,80 mg of tetrakis (triphenylphosphine) palladium (0), 5 mL of dry DMF, and 5 mL of dry THF. The mixture is stirred and heated at 55 °C while a slow stream of carbon monoxide is introduced below the surface of the liquid using a long 18 gauge needle. To the mixture is added, via syringe pump over about 5 h, a solution of 0.32 mL of tri-n-butylstannane in 10 mL of dry THF. Following the addition, solvents are removed in vacuo, and the remaining solid is washed with several portions of EtOAc and ether, and then dried under vacuum to provide 393 mg of the aldehyde as a poorly soluble tan solid.

NMR (DMSO-d6) 8 4.58,4.75,4.98,5.76,7.3,7.70,7.78,7.95,8.45,8.64,8.93,10.10, 10. 24.

TLC Rf 0. 44 (3% MeOH in dichoromethane).

Example 33: N- (4-Chlorobenzyl)-9- (4-morpholinylmethyl)-7-oxo-2- (2-pyridinyl)-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (I-6 of Chart I, T=2-pyridyl) A mixture of 138 mg of aldehyde 1-5 of Preparation 41,79 pL of morpholine, and 34 pL of acetic acid in 3.0 mL of dry THF is stirred at ambient temperature for 30 minutes, then 50 mg of sodium triacetoxyborohydride is added. After 30 min, a second 50 mg portion of triacetoxyborohydride is added, and the resulting mixture stirred overnight. The following day, additional portions of triacetoxyborohydride sufficient to result in complete

reduction are added over the course of 8 h. The reaction is partitioned between CH2Cl2 and aqueous sodium bicarbonate, and the aqueous phase is extracted with additional CH2Cl2.

The combined organic phases are dried (Na2S04) and concentrated under reduced pressure, and the residue flash chromatographed on silica using 3% MeOH in CH2C12 to afford 152 mg of the product as a white solid.. Recrystallization from 10 mL of acetonitrile provides 129 mg of the title compound as fine needles, mp 208-216 °C.

'NMR (CDC13) 8 2.47,3.61,3.72,4.58,4.64,4.72,5.51,7.3,7.5 L 7.63,7.79,7.97,8.63, 8.72,10.44.

TLC Rf 0. 38 (5% MeOH in CH2Cl2).

IR3035, 1655,1608,1569,1551,1499,1452,1410,1357,1346,1329,1283,1212, 1113, 810 cm-1 OAMS supporting ions at: ESI+ 531.2 HRMS (FAB) 531.1813 Anal. found: C, 65.39; H, 5.13; N, 10.47.

Example 34: N- (4-Chlorobenzyl)-9- (4-morpholinylmethyl)-7-oxo-2- (3-pyridinyl)-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (I-6 of Chart I, T=3-pyridyl) Following the procedures in Preparations 37-41 and Example 33 without making major changes except using 3-pyridylcarboxaldehyde as a starting material, the title compound is obtained as solid.

IH NMR (CDCl3) 8 2.47,3.61,3.71,4.33,4.43,4.63,5.38,7.30,7.45,7.85,8.00,8.69, 8.74,8.79,10.40.

TLC Rf 0. 28 (5% MeOH in CH2Cl2).

IR 3038, 1656,1607,1580,1553,1498,1457,1409,1345,1331,1320,1282,1115, 810, 711 cm-1 OAMS supporting ions at: ESI+ 531.2 HRMS (FAB) 531.1798 Anal. found: C, 65.62; H, 5.18; N, 10.53.

Example 35: N- (4-Chlorobenzyl)-9- (4-morpholinylmethyl)-7-oxo-2- (4-pyridinyl)-2, 3- dihydro-7H- [1, 4] oxazino [2, 3,4-ij] quinoline-6-carboxamide (I-6 of Chart I, T=4-pyridyl)

Following the procedure in Preparations 37-41 and Example 33 without making major changes except using 4-pyridylcarboxaldehyde as a starting material, the title compound is obtained as solid. lH NMR (CDC13) õ 2.47,3.61,3.71,4.25,4.49,4.60,5.34,7.27,7.45,7.49,7.99,8.70, 8.74,10.41.

TLC Rf 0. 26 (5% MeOH in CH2Cl2).

IR 2859, 1666,1608,1551,1500,1411,1352,1331,1285,1271,1220,1114,1090, 821, 806 cm-1 OAMS supporting ions at: ESI+ 531.2 HRMS (FAB) 531.1791 Anal. found: C, 65.26; H, 5.18; N, 10.50.

Preparation 42: Ethyl 8-fluoro-4-hydroxy-6-iodoquinoline-3-carboxylate (Formula M-2 of Chart M) A mixture of 2-fluoro-4-iodoaniline (11.85 g) and diethylethoxymethylene malonate (10.81 g) is heated to 130 °C in a flask equipped with a Dean-Stark trap to collect EtOH formed. The mixture is then cooled to 75 °C and diluted with hexanes. The resulting solid is collected and dried. The solid is then dissolved in 60 mL Ph20 and heated to 250 °C for 3 h in a flask equipped with a Dean-Stark-trap to collect the EtOH formed. The solution is allowed to cool to room temperature and the resulting solid is collected and dried to yield 11.73 g of ethyl-8-fluoro-4-hydroxy-6-iodoquinoline-3-carboxylate.

M. p. 287-289 °C 'H NMR (DMSO-d6) 8 12.60,8.38,8.23,8.04,4.22,1.28

IR (drift) 3165,3080,3070,3059,2969,1709,1616,1603,1564,1527,1296,1249, 1173, 1141,865 cri' HRMS (FAB) calcd for Cl2HgFINO3+Hl 361.9691, found 361.9696 Anal. Calcd for C12H9FINO3 : C, 39.91; H, 2.51; N, 3.88. found: C, 39.71; H, 2.42; N, 3.88.

Preparation 43: N- (4-Chlorobenzyl)-8-fluoro-4-hydroxy-6-iodoquinoline-3- carboxamide (Formula M-3 of Chart M) Compound M-2 of Preparation 42 (0.55 g) and 4-chlorobenzylamine (3 mL) are heated at 180 °C for 1 h. The reaction is cooled and poured into 75 mL diethyl ether. The resulting solid is filtered and recrystallized from EtOAc/hexanes to give the product as an off-white solid (0.45 g), m. p. 268-270 °C 'H NMR (DMSO-d6) 8 10. 17,8.59,8.29,8.05,7.37,7.33,4.51 IR (mull) 3180,3078,3059,3004,1647,1607,1551,1524,1489,1344,1297,1285, 1240, 1183, 805 caf ; MS (ESI) for m/z 456.9 (M+H) +, 454.9 (M-H)- HRMS (FAB) calcd for C17H11ClFIN2O2+H1 456.9618, found 456.9628 Anal. Calcd for C17HICIFIN202 : C, 44.72; H, 2.43; N, 6.14. found: C, 45.45; H, 2.82; N, 6.05.

Preparation 44: N- (4-Chlorobenzyl)-8-fluoro-6-formyl-4-hydroxyquinoline-3- carboxamide (Formula M-4 of Chart M) A mixture of 4.57 g of compound M-3 of Preparation 43 and 810 mg of tetrakis (triphenylphosphine) palladium (0) in 35 mL of dry DMF and 10 mL of dry THF is stirred and purged with CO for 10 minutes, and then heated to 60 °C. Passage of CO through the mixture is continued while 3.3 mL of tributyltin hydride in 6.7 mL of dry THF is added very slowly, via syringe pump over about 6 h. The reaction mixture is then cooled and concentrated under reduced pressure to a semisolid. Ether (70 mL) is added and the resulting solid filtered, washed well with ether, and dried in vacuo to provide 3.54 g of the aldehyde.

'H NMR (CDC13 + CD30D) 8 4.65,7.32,7.93,8.68,8.75,10.07,10.43 ppm.

TLC Rf 0. 29 (3% methanol in dichloromethane).

OAMS supporting ions at: ESI-358.1.

Preparation 45: N- (4-Chlorobenzyl)-8-fluoro-4-hydroxy-6- (morpholin-4- ylmethyl) quinoline-3-carboxamide (Formula M-5 of Chart M) To a stirred solution of 2.42 g of aldehyde M-4 of Preparation 44 in 50 mL of THF is added 1.8 mL of morpholine and 0.77 mL of acetic acid. The resulting slurry is stirred well for 15 min, then 1.42 g of sodium triacetoxyborohydride is added. Additional portions of triacetoxyborohydride are periodically added until TLC analysis indicates completion of reaction. The reaction is then partitioned between dichloromethane and aqueous NaHCO3, and the aqueous phase extracted with additional dichloromethane. The combined organic extract is dried (Na2S04) and concentrated under reduced pressure. Flash chromatography of the residue on silica gel using 4-5% methanol in dichloromethane affords 2.29 g of the title compound as a tan solid. Recrystallization from acetonitrile provides tan plates, mp 227.5-230.0 °C.

1H NMR (CDC13 + CD30D) 8 2.47,3.62,3.72,4.64,7. 31,7.56,8.06,8.70,10.63 ppm.

TLC Rf 0. 33 (5% methanol in dichoromethane).

IR (diffuse reflectance) 3080,3025,2971,2929,2861,1660,1613,1575,1542,1508,1349, 1268,1118,806,799 cm' OAMS supporting ions at: ESI+ 430.3 HRMS (FAB) calcd for C22H21CLFN303 +Hl 430.1334, found 430.1339 Anal. Calcd for C22H21ClFN303 : C, 61.47; H, 4.92; N, 9.77; Cl, 8.25; F, 4.42; found: C, 61.09; H, 4.92; N, 9.66.

Preparation 46: General procedure for preparation of epoxides (M-7) Step 1: Trimethylsulfonium methylsulfate: Dimethyl sulfide (25.0 mL) is cooled to 0 °C, and dimethyl sulfate (25.0 mL) is added. The liquid is stirred at 0 °C and allowed to warm slowly as the ice in the cooling bath melts. The following day, ether is added and the solid mass crushed with a stirring rod. The solid is filtered, washed well with ether, and dried iii vacuo to provide 48.0 g of the salt as a white crystalline solid.

Step 2: Epoxidation : 3-Oxiran-2-ylbenzonitrile (Formula M-7 of Chart M, where Ra=3-cyanophenyl and Rb=H) To a solution of 1.31 g of 3-cyanobenzaldehyde (Formula M-6 of Chart M where Ra is 3-cyanophenyl and Rb is H) and 25 mg of tetra-n-butylammonium bromide in 30 mL of dichloromethane is added a solution of 3.92 g of trimethylsulfonium methylsulfate in 10 mL of water, followed by 20 mL of 50% aqueous NaOH. The biphasic mixture is stirred and

refluxed for 5 h, then cooled, diluted with brine (-20 mL) and ether ("50 mL), and filtered to remove solids. The phases are separated and the aqueous phase extracted with additional ether as necessary to remove product. The combined organic phase is dried (Na2SO4) and concentrated under reduced pressure, or at atmospheric pressure through a Vigreux column.

Kugelrohr distillation of the residue at ca. 0.5 mmHg and 160 °C oven temperature affords 1.20 g of the epoxide as a colorless liquid.

1H NMR (CDC13) b 2.76,3.19,3.90,7.47,7.52,7.58,7.70 ppm.

OAMS supporting ions at: ESI-144.0 Using the general procedure of Preparation 46, the following epoxides (M-7) are obtained.

3-Oxiran-2-ylfuran (Formula M-7 of Chart M, where Ra=furan-3-yl and Rb=H) As a colorless liquid following kugelrohr distillation at ca. 0.5 mmHg and 40 °C oven temperature. lH NMR (CDC13) 8 2.88,3.11,3.80,6.28,7.39,7.52 ppm.

OAMS supporting ions at: ESI+ 111.2.

2-Thien-2-yloxirane (Formula M-7 of Chart M, where Ra=thien-2-yl and Rb=H) As a colorless liquid following kugelrohr distillation at ca. 0.5 mmHg and 75 °C oven temperature.

'H NMR (CDC13) 8 3.00,3.19,4.10,6.98,7.13,7.25 ppm.

OAMS supporting ions at: ESI+ 127.1.

2- (3, 5-Difluorophenyl) oxirane (Formula M-7 of Chart M, where Ra=3,5-difluorophenyl and Rb=H) As a colorless liquid following kugelrohr distillation at ca. 0.5 mmHg and 75 °C oven temperature.

'H NMR (CDC13) 8 2.72,3.15,3.84,6.73,, 6.81 ppm.

5-Oxiran-2-yl-1, 3-benzodioxole (Formula M-7 of Chart M, where Ra=1, 3-benzodioxol-5- yl and Rb=H)

As a colorless liquid following kugelrohr distillation at ca. 0.5 mmHg and 150 °C oven temperature.

'H NMR (CDC13) 8 2.75,3.10,3.79,5.95,6.7,6.8 ppm.

OAMS supporting ions at: ESI+ 165.2.

6-Oxiran-2-yl-2, 3-dihydro-1, 4-benzodioxine (Formula M-7 of Chart M, where Ra=2, 3- dihydro-1, 4-benzodioxin-6-yl and Rb=H) As a colorless oil following kugelrohr distillation at ca. 0.5 mmHg and 175 °C oven temperature.

'H NMR (CDC13) 8 2.75,3.08,3.75,4.23,6.76,6.83 ppm.

OAMS supporting ions at: ESI+ 179.2.

4-Oxiran-2-yl-1, 3-benzodioxole (Formula M-7 of Chart M, where Ra=1, 3-benzodioxol-4- yl and Rb=H) As a colorless liquid following kugelrohr distillation at ca. 0.5 mmHg and 125 °C oven temperature.

'H NMR (CDC13) 8 3.02,3.14,3.96,5.97,6.00,6.70,6.8 ppm.

2- [3, 5-bis (Methoxymethoxy) phenyl] oxirane (Formula M-7 of Chart M, where Ra=3, 5- bis (methoxymethoxy) phenyl and Rb=H) As a colorless liquid following kugelrohr distillation at ca. 0.5 mmHg and 200 °C oven temperature.

1H NMR (CDC13) 8 2.76,3.11,3.47,3.81,5.14,5.16,6.63,6.67 ppm.

OAMS supporting ions at: ESI+ 241.2.

2- [2, 3-bis (Methoxymethoxy) phenyl] oxirane (Formula M-7 of Chart M, where Ra=2,3- bis (methoxymethoxy) phenyl and Rb=H) As a colorless liquid following kugelrohr distillation at ca. 0.5 mmHg and 200 °C oven temperature.

'H NMR (CDC13) 8 2.74,3.16,3.50,3.60,4.28,5.17,5.19,5.21,6.81,7.03,7.09 ppm.

OAMS supporting ions at: ESI-239. 1.

2-Thien-3-yloxirane (Formula M-7 of Chart M, where Ra=thien-3-yl and Rb=H)

As a colorless liquid following kugelrohr distillation at ca. 0.5 mmHg and 75 °C oven temperature.

1H NMR (CDC13) 8 2.90,3.13,3.93,6.96,7.29 ppm.

OAMS supporting ions at: ESI+ 127.1.

1, 6-Dioxaspiro [2.5] octane (Formula M-7 of Chart M, where Ra, Rb=4-tetrahydropyran) As a colorless liquid following kugelrohr distillation at ca. 0.5 mmHg and 100-200 °C oven temperature. The poor yield is thought to be due to troublesome distillation behavior, with sequestering of product in the viscous pot residue. lH NMR (CDC13) õ 1.54,1.87,2.70,3.84 ppm.

6-Methyl-l-oxa-6-azaspiro [2.5] octane (Formula M-7 of Chart M, where Ra, Rb=N- methyl-4-piperidine) As a colorless liquid following kugelrohr distillation at ca. 0.5 mmHg and 50 °C oven temperature.

'H NMR (CDC13) 8 1.56,1.87,2.34,2.5,2.66 ppm.

OAMS supporting ions at: ESI+ 128.2.

1, 7,10-Trioxadispiro [2.2.4. dodecane (Formula M-7 of Chart M, where Ra, Rb=cyclohexane-4-ethylene ketal) As a white crystalline solid, melting at slightly above room temperature, following kugelrohr distillation at ca. 0.5 mmHg and 130 °C oven temperature.

'H NMR (CDCl3) 8 1.58,1.77,1.9,2.68,3.98 ppm.

OAMS supporting ions at: ESI+ 171. 1.

1-Oxa-6-thiaspiro [2.5] octane (Formula M-7 of Chart M, where Ra, Rb=tetrahydrothiopyran) As a white crystalline solid following kugelrohr distillation at ca. 0.5 mmHg and 120 °C oven temperature.

'H NMR (CDCl3) 8 1.74,2.00,2.60,2.65,2.91 ppm.

Preparation 47: tert-Butyl 1-oxa-6-azaspiro [2.5] octane-6-carboxylate (Formula M- 7 of Chart M, where Ra, Rb=N-Boc-4-piperidine)

Step 1: To a stirred mixture of 3.07 g of 4-piperidone hydrochloride hydrate and 4.80 g of di-tert-butyl dicarbonate in 20 mL of THF is added 7.0 mL of 3N aqueous NaOH.

The biphasic mixture is stirred well for 18 h, then diluted with chloroform. The phases are separated and the aqueous phase extracted with one portion of chloroform, and the combined extract dried (Na2SO4) and concentrated under reduced pressure. Flash chromatography of the residue on silica using 10-20% ethyl acetate in dichloromethane provides 4.08 g of tert-butyl 4-oxopiperidine-1-carboxylate (Boc-piperidone) as a white crystalline solid.

'H NMR (CDC13) 8 1.50,2.44,3.72 ppm.

TLC Ru 0. 38 (10% ethyl acetate in dichloromethane).

OAMS supporting ions at: ESI+ 200.1 Step 2: Using the general procedure of Preparation 46, the ketone product of step 1 is converted to the epoxide as a white crystalline solid.

1H NMR (CDC13) 8 1. 45,1.48,1.80,2.70,3.43,3.7 ppm.

OAMS supporting ions at: ESI+ 214.2.

Preparation 48: 2,2-bis [(Methoxymethoxy) methyl] oxirane (Formula M-7 of Chart M, where Ra, Rb=methoxymethoxymethyl) Step 1: To a cold (0 °C), stirred mixture of 3.60 g of dihydroxyacetone dimer and 16 mL of diisopropylethylamine in 40 mL of dichloromethane is added 6.1 mL of chloromethyl methyl ether. The mixture is stirred and allowed to warm slowly to room temperature. After 18 h, the clear solution is partitioned between ether and dilute HC1. The aqueous phase is placed in a continuous extractor and extracted overnight with ether. The combined organic phase is then dried (MgS04) and concentrated under reduced pressure.

Kugelrohr distillation of the residue at ~0. 5 mmHg and 150 °C oven temperature affords 2.79 g of 2,4,8,10-tetraoxaundecan-6-one as a pale yellow oil.

'H NMR (CDC13) 8 3.40,4.34,4.69 ppm.

Step 2: Using the general procedure of Preparation of 46, the ketone product of Step 1 is converted to the epoxide as a white crystalline solid after kugelrohr distillation at ca.

0.5 mmHg and 150 °C oven temperature.

'H NMR (CDC13) 8 2.83,3.37,3.72,4.65 ppm. Example 36: General procedure for epoxide alkylation: N- (4-Chlorobenzyl)-2- (3- cyanophenyl)-9- (morpholin-4-ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4- ij] quinoline-6-carboxamide (Formula M-8 of Chart M, where Ra=3-cyanophenyl and Rb=H)

To a mixture of 172 mg of fluorodihydroquinoline M-5 of Preparation 45 and 261 mg of cesium carbonate in 1 mL of DMF is added 116 mg of 3-oxiran-2-ylbenzonitrile (Formula M-7 of Chart M where Ra is 3-cyanophenyl and Rb is H). The mixture is stirred and heated at 90 °C for 4-5 h, and then a second 116 mg portion of epoxide is added and heating continued overnight. The reaction is then cooled and partitioned between chloroform and water, and the aqueous phase extracted with additional chloroform as needed to remove product. The combined organic phase is dried (Na2S04) and concentrated under reduced pressure, and the residue chromatographed on silica gel using 2.5-3.5% methanol in dichloromethane to afford 125 mg of the title compound.

Recrystallization from acetonitrile provides orange needles.

1H NMR (CDC13 + CD30D) 8 2.49,3.63,3.73,4.26,4.59,4.63,5.40,7.30,7.50,7.64, 7.78,7.90,7.99,8.65,10.54 ppm.

TLC Rf 0. 40 (5% methanol in dichloromethane).

OAMS supporting ions at: ESI+ 555.3.

Example 37 N- (4-Chlorobenzyl)-2- (3-furyl)-9- (morpholin-4-ylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula M-8 of Chart M, where Ra=furan-3-yl and Rb=H)

The title compound is prepared according to the general procedure of Example 36, and is purified by flash chromatography on silica gel using 2% methanol in dichloromethane. Recrystallization from acetonitrile provides tan crystals, mp 193-196 °C.

IH NMR (CDC13) 8 2.46,3.59,3.70,4.34,4.41,4.63,5.37,6.49,7.30,7.41,7.51,7.60, 7.96,8.67,10.44 ppm.

TLC Rf 0. 22 (3% methanol in dichloromethane).

IR (diffuse reflectance) 1655,1627,1608,1569,1551,1500,1411,1347,1329,1282,1218, 1114,885,875,809 cm~l OAMS supporting ions at: ESI+ 520.4 HRMS (FAB) calcd for C28H26CLN305 +Hl 520.1639, found 520.1634 Anal. Calcd for C28H26ClN305 : C, 64.68; H, 5.04; N, 8.08; Cl, 6.82; found: C, 64.50; H, 5.09; N, 8.05.

Example 38: N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2-thien-2-yl-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula M-8 of Chart M, where Ra=thien-2-yl and Rb=H) The title compound is prepared according to the general procedure of Example 36, and is purified by flash chromatography on silica gel using 2% methanol in dichloromethane. Recrystallization from acetonitrile provides pale yellow crystals.

IH NMR (CDC13) 8 2.46,3.59,3.70,4.44,4.50,4.63,5.64,7.09,7.20,7.30,7.44,7.98, 8.68,10.43 ppm.

TLC Rf 0. 28 (3% methanol in dichloromethane).

IR (diffuse reflectance) 2954,2926,2799,1666,1610,1568,1551,1500,1343,1287,1275, 1110,887,860,798 cm' OAMS supporting ions at: ESI+ 536.3 HRMS (FAB) calcd for C28H26CLN304S +Hl 536.1411, found 536. 1411 Anal. Calcd for C28H26ClN304S : C, 62.74; H, 4.89; N, 7.84; Cl, 6.61; S, 5.98; found: C, 62.72; H, 4.92; N, 7.86. Example 39: N- (4-Chlorobenzyl)-2- (3, 5-difluorophenyl)-9- (morpholin-4-ylmethyl)-7- oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxaniide (Formula M-8 of Chart M, where Ra=3, 5-difluorophenyl and Rb=H)

The title compound is prepared according to the general procedure of Example 36, and is purified by flash chromatography on silica gel using 2% methanol in dichloromethane. Recrystallization from acetonitrile containing about 10% methanol affords white crystals, mp 234-236 °C.

1H NMR (CDC13) 8 2.47,3.61,3.71,4.23,4.41,4.63,5.30,6.91,7.06,7.29,7.48,8.00, 8.67,10.40 ppm.

TLC Rf 0. 32 (3% methanol in dichloromethane).

IR (diffuse reflectance) 1650,1628,1603,1575,1552,1532,1500,1466,1452,1411,1347, 1281,1121,864,811 cri' OAMS supporting ions at: ESI+ 566.4 HRMS (FAB) calcd for C3oH26CLF2N304 +Hl 566.1658, found 566.1654 Anal. Calcd for C3oH26ClF2N304 : C, 63.66; H, 4.63; N, 7.42; Cl, 6.26; F, 6.71; Found: C, 63.22; H, 4.73; N, 7.82.

Example 40: 2- (1, 3-Benzodioxol-5-yl)-N- (4-chl6robenzyl)-9- (morpholin-4-ylmethyl)- 7-oxo-2,3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula M-8 of Chart M, where Ra=1, 3-benzodioxol-5-yl and Rb=H) The title compound is prepared according to the general procedure of Example 36, and is purified by flash chromatography on silica gel using 2-3% methanol in

dichloromethane. Recrystallization from acetonitrile containing about 10% methanol affords pale yellow crystals, mp 227-231 °C.

'H NMR (CDC13 + CD30D) 8 2.49,3.62,3.72,4.29,4.47,4.63,5.24,6.04,6.90,6.98, 7. 31, 7.45,7.95,8.64,10.59 ppm.

TLC Rf 0. 30 (3% methanol in dichloromethane).

IR (diffuse reflectance) 1650,1627,1608,1552,1500,1449,1411,1353,1330,1282,1246, 1225,1116,1038, 810 cm-1 OAMS supporting ions at: ESI+ 574.4 HRMS (FAB) calcd for C3lH28CLN306 +HI 574.1744, found 574.1760 Anal. Calcd for C3lH28ClN306 : C, 64.86; H, 4.92; N, 7. 32 ; Cl, 6.18; found: C, 64.75; H, 4.96; N, 7.24.

Example 41: N- (4-Chlorobenzyl)-2- (2, 3-dihydro-1, 4-benzodioxin-6-yl)-9- (morpholin- 4-ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula M-8 of Chart M, where Ra=2,3-dihydro-1,4-benzodioxin-6-yl and Rb=H) The title compound is prepared according to the general procedure of Example 36, and is purified by flash chromatography on silica gel using 2% methanol in dichloromethane. Recrystallization from acetonitrile containing about 10% methanol affords white crystals, mp 240-243 °C. lH NMR (CDC13 + CD30D) 8 2.48,3.62,3.72,4.29,4.31,4.43,4.63,5.21,6.96,7.02, 7.31,7.44,7.95,8.64,10.57 ppm.

TLC Rf 0. 30 (3% methanol in dichloromethane).

IR (diffuse reflectance) 1648, 1607,1552,1502,1411,1330,1308,1293,1281,1261,1120, 1116,1068,891, 811 cm-1 OAMS supporting ions at: ESI+ 588.4 HRMS (FAB) calcd for C32H30CLN306 +Hi 588.1901, found 588.1905 Anal. Calcd for C32H30ClN306 : C, 65.36; H, 5.14; N, 7.14; Cl, 6.03; found: C, 65.15; H, 5.19; N, 7.04.

Example 42: 2- (1, 3-Benzodioxol-4-yl)-N- (4-chlorobenzyl)-9- (morpholin-4-ylmethyl)- 7-oxo-2,3-dihydro-7H- [l, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula M-8 of Chart M, where Ra=1, 3-benzodioxol-4-yl and Rb=H)

The title compound is prepared according to the general procedure of Example 36, and is purified by flash chromatography on silica gel using 2% methanol in dichloromethane. Recrystallization from acetonitrile containing about 10% methanol affords white crystals, mp 221-225 °C (d).

1H NMR (CDC13) 8 2.46,3.60,3.70,4.43,4.48,4.63,5.45,6.02,6.07,6.91,6.95,7.02, 7.3, 7.46,7.97,8.68,10.45 ppm.

TLC Rf 0. 30 (3% methanol in dichloromethane).

IR (diffuse reflectance) 1654,1606,1553,1498,1463,1411,1349,1283,1272,1249,1223, 1119,871,808,797 cm-1 OAMS supporting ions at: ESI+ 574.4 HRMS (FAB) calcd for C3lH28CLN306 +Hl 574.1744, found 574.1763 Anal. Calcd for C31H28CIN306 : C, 64.86; H, 4.92; N, 7.32; Cl, 6.18; found: C, 64.77; H, 4.98; N, 7.37.

Example 43 2- [3, 5-bis (Methoxymethoxy) phenyl]-N- (4-chlorobenzyl)-9- (morpholin-4- ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula M-8 of Chart M, where Ra=3,5-bis (methoxymethoxy) phenyl and Rb=H)

The title compound is prepared according to the general procedure of Example 36, and is purified by flash chromatography on silica gel using 2% methanol in dichloromethane.

Recrystallization from acetonitrile affords pale pink crystals, mp 187-189 °C.

'H NMR (CDC13) 8 2.47,3.50,3.60,3.71,4.29,4.37,4.63,5.18,5.21,5.23,6.82,7.3,7 .46, 7.97,8.66,10.45 ppm.

TLC Rf 0. 33 (3% methanol in dichloromethane).

IR (diffuse reflectance) 3031,2937,2922,1655,1607,1578,1569,1551,1499,1288,1147, 1086, 1025,1011,925 cm~l OAMS supporting ions at: ESI+ 650.5 HRMS (FAB) calcd for C34H36CLN308 +Hl 650.2269, found 650.2283 Anal. Calcd for C34H36ClN3Og : C, 62.81; H, 5.58; N, 6.46; Cl, 5.45; found: C, 62.63; H, 5.59; N, 6.45.

Example 44: 2- [2, 3-bis (Methoxymethoxy) phenyl]-N- (4-chlorobenzyl)-9- (morpholin-4- ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula M-8 of Chart M, where Ra=2,3-bis (methoxymethoxy) phenyl and Rb=H) The title compound is prepared according to the general procedure of Example 36, and is purified by flash chromatography on silica gel using 2% methanol in dichloromethane. Recrystallization from acetonitrile affords white crystals, mp 177-180 °C.

'H NMR (CDC13) 8 2.47,3.45,3.53,3.61,3.71,4.16,4.60,4.64,5.18,5.21,5.25,5.70, 7.2, 7.3,7.46,7.99,8.67,10.49 ppm.

TLC Rf 0. 40 (3% methanol in dichloromethane).

IR (diffuse reflectance) 1648,1605,1571,1551,1526,1500,1482,1280,1260,1159,1115, 1077,1004,957,924 ciri i OAMS supporting ions at: ESI+ 650.5 HRMS (FAB) calcd for C34H36CLN3O8 +H1 650.2269, found 650.2279 Anal. Calcd for C34H36ClN3Og : C, 62.81; H, 5.58; N, 6.46; Cl, 5.45; found: C, 62.63; H, 5.57; N, 6.39.

Example 45: N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2-thien-3-yl-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula M-8 of Chart M, where Ra=thien-3-yl and Rb=H)

The title compound is prepared according to the general procedure of Example 36, and is purified by flash chromatography on silica gel using 2% methanol in dichloromethane. Recrystallization from acetonitrile affords yellow crystals, mp 241-245 °C (d).

'H NMR (CDC13) 8 2.46,3.60,3.70,4.37,4.44,4.63,5.45,7.19,7.3,7.44,7.47,7.97,8 .68, 10.44 ppm.

TLC Rf 0. 35 (3% methanol in dichloromethane).

IR (diffuse reflectance) 1656,1627,1608,1569,1551,1500,1411,1348,1330,1319,1282, 1227,1113,810,797 cm-1 OAMS supporting ions at: ESI+ 536.4 HRMS (FAB) calcd for C28H26CLN304S +Hl 536.1411, found 536.1417 Anal. Calcd for C28H26ClN304S : C, 62.74; H, 4.89; N, 7.84; Cl, 6.61; S, 5.98; found: C, 62.68; H, 4.94; N, 7.77.

Example 46: N- [ (4-Chlorophenyl) methyl]-2, 3,5,6-tetrahydro-9'- (4- morpholinylmethyl)-7'-oxospiro [4H-pyran-4, 21 (3'H)- [7H] pyrido [1, 2,3-de] [1, 4] benzoxazine]-6'-carboxamide (Formula M-8 of Chart M, where Ra, Rb=4- tetrahydropyran)

The title compound is prepared according to the general procedure of Example 36, and is purified by flash chromatography on silica gel using 3% methanol in dichloromethane. Recrystallization from acetonitrile affords white crystals, mp 251-254 °C.

'H NMR (CDC13) 81. 80,2.47,3.59,3.72,3.86,4.04,4.64,7.30,7.40, 7.94,8.65,10.44 ppm.

TLC Rf 0. 30 (5% methanol in dichloromethane).

IR (diffuse reflectance) 2861,1655,1607,1568,1552,1504,1411,1323,1277,1245,1217, 1113,1015,882, 811 cm-1 OAMS supporting ions at: ESI+ 524.4 HRMS (FAB) calcd for CzsHsoCLNsOs +Hl 524.1952, found 524.1957 Anal. Calcd for C28H30ClN3O5 : C, 64.18; H, 5.77; N, 8.02; Cl, 6.77; found: C, 64.12; H, 5.78; N, 8.03.

Example 47: 1, 1-Dimethylethyl 6-[[[(4-chlorophenyl) methyl] amino] carbonyl]-9'- (4- morpholinylmethyl)-7'-oxospiro [piperidine-4, 2' (3'I)- [7H] pyrido [1,2,3-de] [1, 4] benzoxazine]-1-carboxylate (Formula M-8 of Chart M, where Ra, Rb=N-Boc-4- piperidine) The title compound is prepared according to the general procedure of Example 36, and is purified by flash chromatography on silica gel using 2% methanol in dichloromethane. Recrystallization from acetonitrile affords white crystals, mp 213 °C (d).

1H NMR (CDC13) 8 1. 47,1.67,1.81,2.46,3.23,3.59,3.71,3.97,4.03,4.64,7.30,7.38, 7.94,8.63,10.43 ppm.

TLC Rf 0. 45 (5% methanol in dichloromethane).

IR (diffuse reflectance) 1694,1662,1647,-1605,1570,1551,1537,1500,1413,1366,1281, 1249,1151,1113, 811 cm-1 OAMS supporting ions at: ESI+ 623.5 HRMS (FAB) calcd for C33H39CLN406 +Hi 623.2636, found 623.2628

Anal. Calcd for C33H39C1N406 : C, 63.61; H, 6.31; N, 8.99; Cl, 5.69; found: C, 63.38; H, 6.30; N, 9.02.

Example 48: N- [ (4-Chlorophenyl) methyl]-9'- (4-morpholinylmethyl)-7'- oxospiro [piperidine-4,21 (3'H)- [7H] pyrido [1,2,3-de] [1, 4] benzoxazine]-6'-carboxamide (Formula M-8 of Chart M, where Ra, Rb=4-piperidine) A solution of 102 mg of the product of Example 47 in 1 mL of 1: 1 TFA- dichloromethane is allowed to stand for 1 h, then partitioned between excess aqueous NaHCO3 and dichloromethane. The organic phase is dried (Na2S04) and concentrated under reduced pressure. Flash chromatography of the residue on silica using 5-8% methanolic ammonia in dichloromethane provides 73 mg of the title compound as a white solid. Recrystallization from acetonitrile containing ca. 10% methanol affords white crystals, mp 246-250 °C (d).

1H NMR (CDC13) b 1.68,1.80,2.46,2.92,3.08,3.59,3.71,4.03,4.64,7.30,7.38,7.92, 8.64,10.47 ppm.

TLC Rf0. 25 (8% methanolic ammonia in dichloromethane).

IR (diffuse reflectance) 2963,2936,2916,1655,1607,1569,1551,1503,1411,1322,1281, 1218,1113, 882, 811 cm-1 OAMS supporting ions at: ESI+ 523.5 HRMS (FAB) calcd for C28H3lCLN404 +HI 523.2112, found 523.2122 Anal. Calcd for C28H3lClN404 : C, 64.30; H, 5.97; N, 10.71; Cl, 6.78; found: C, 64.08; H, 6.04; N, 10.76.

Example 49: N-[(4-Chlorophenyl)methyl]-1-methyl-9'-(4-morpholinylmethyl) -7'- oxospiro [piperidine-4, 21 (3'H)- [7H] pyrido [1, 2,3-de] [1, 4] benzoxazine]-6'-carboxamide (Formula M-8 of Chart M, where Ra, Rb=N-methyl-4-piperidine)

The title compound is prepared according to the general procedure of Example 36, and is purified by flash chromatography on silica gel using 3% methanolic ammonia in dichloromethane. Recrystallization from acetonitrile affords fine white needles, mp 234-237 °C (d).

'H NMR (CDC13) § 1.83,2.36,2.46,2.64,3.59,3.72,4.02,4.64,7.30,3.38,7.93,8.64, 10.45 ppm.

TLC Rf 0. 41 (5% methanolic ammonia in dichloromethane).

IR (diffuse reflectance) 2951,2938,2797,1653,1607,1552,1501,1413,1306,1289,1276, 1216,1144,1116,811 crif 1 OAMS supporting ions at: ESI+ 537.2 HRMS (FAB) calcd for C29H33CLN4O4 +H1, 537.2268, found 537.2271 Anal. Calcd for C29H33ClN404 : C, 64.86; H, 6.19; N, 10.43; Cl, 6.60; found: C, 64.73; H, 6.16; N, 10.36.

Example 50 N- [ (4-Chlorophenyl) methyl]-9"- (4-morpholinylmethyl) dispiro [1, 3- dioxolane-2, 1'-cyclohexane-4',2''(3''H)-[7H] pyrido [1, 2,3-de] [1, 4] benzoxazine]-6"- carboxamide (Formula M-8 of Chart M, where Ra, Rb=cyclohexane-4-ethylene ketal) The title compound is prepared according to the general procedure of Example 36, and is purified by flash chromatography on silica gel using 2% methanol in dichloromethane. Recrystallization from acetonitrile affords white crystals, mp >260 °C.

1H NMR (CDC13) 8 1.66,1.84,2.01,2.46,3.58,3.71,3.99,4.02,4.64,7.30,7.36,7.92, 8.63,10.47 ppm.

TLC Rif 0. 43 (5% methanol in dichloromethane).

IR (diffuse reflectance) 2958,2933,1649,1606,1568,1551,1503,1412,1286,1272,1256, 1116,1102,917, 810 cm-1 OAMS supporting ions at: ESI+ 580.3 HRMS (FAB) calcd for C3lH34CLN306 +Hl 580.2214, found 580.2227 Anal. Calcd for C31H34ClN3O6: C, 64.19; H, 5.91; N, 7.24; Cl, 6.11; found: C, 64.15; H, 5.92; N, 7.13.

Example 51: N- (4-Chlorobenzyl)-2, 2-bis [(methoxymethoxy) methyl]-9-(morpholin-4- ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula M-8 of Chart M, where Ra, Rb=methoxymethoxymethyl) The title compound is prepared according to the general procedure of Example 36, and is purified by flash chromatography on silica gel using 2% methanol in dichloromethane. Recrystallization from ethyl acetate affords white crystals, mp 147-149 °C.

'H NMR (CDCl3) 8 2.45,3.33,3.57,3.66,3.70,3.77,4.33,4.63,4.64,7.31,7.38,7.94, 8.67,10.45 ppm.

TLC Rf 0. 40 (5% methanol in dichloromethane).

IR (diffuse reflectance) 2954,2931,2888,1653,1608,1569,1552,1501,1411,1280,1150, 1113,1045,919,809 cm~ OAMS supporting ions at: ESI+ 602.2 HRMS (FAB) calcd for C3oH36CLN308 +Hl 602.2269, found 602.2269 Anal. Calcd for C30H36ClN3O8: C, 59.85; H, 6.03; N, 6.98; Cl, 5.89; found: C, 59.77; H, 5.96; N, 6.95.

Example 52: N- (4-Chlorobenzyl)-2, 2-bis (hydroxymethyl)-9- (morpholin-4-ylmethyl)- 7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide (Formula M-8 of Chart M, where Ra, Rb=hydroxymethyl)

A mixture of 151 mg of the product of Example 51 in 2 mL of THF and 1 mL of conc. HC1 is stirred for 18 h, then partitioned between chloroform and excess aqueous NaHC03. The organic phase is dried (Na2SO4) and concentrated under reduced pressure.

Flash chromatography of the residue on silica gel using 7-10% methanol in dichloromethane affords 104 mg of the title compound as a white solid. Trituration and recrystallization from acetonitrile provides white solid with mp 230-233 °C.

'H NMR (CDC13 + CD30D + TFA-d6) 8 3.05,3.40,3.70,3.78,3.9,4.33,4.39,4.64,7.31, 7.49,7.90,8.73 ppm.

TLC Rf 0. 24 (10% methanol in dichloromethane).

IR (diffuse reflectance) 1653,1606,1561,1500,1411,1353,1327,1288,1242,1232,1111, 1058,886,811,795 cm-1 OAMS supporting ions at: ESI+ 514.3 HRMS (FAB) calcd for C26H28CLN306 +Hl 514.1744, found 514.1745 Anal. Calcd for C26H28CIN306 : C, 60.76; H, 5.49; N, 8.18; Cl, 6.90; found: C, 60.52; H, 5.60; N, 8.22.

Example 53: N-[(4-Chlorophenyl) methyl]-2', 3', 5', 6'-tetrahydro-9-(4- morpholinylmethyl)-7-oxospiro [7H-pyrido [1, 2,3-de]-1,4-benzoxazine-2 (3H), 4'- [4H] thiopyran]-6-carboxamide (Formula M-8 of Chart M, where Ra, Rb=4- tetrahydrothiopyran) The product is prepared according to the general procedure of Example 36, and is purified by flash chromatography on silica gel using 2% methanol in dichloromethane.

Recrystallization from ethyl acetate affords white crystals, mp 147-149 °C.

'H NMR (CDC13) õ 1. 88, 2.14,2.47,3.11,3.59,3.72,3.99,4.64,7.30,7.40,7.94,8.63, 10.43 ppm.

TLC Rf0. 35 (3% methanol in dichloromethane).

IR (diffuse reflectance) 1652,1607,1556,1503,1412,1330,1317,1285,1270,1245,1229, 1193,1112,810,798 cm-1 OAMS supporting ions at: ESI+ 540.1 HRMS (FAB) calcd for C28H30CLN304S +Hl 540.1724, found 540.1722 Anal. Calcd for C28H30ClN304S : C, 62.27; H, 5.60; N, 7.78; Cl, 6.56; S, 5.94; found: C, 61.98; H, 5.71; N, 7.67.

Example 54: N- [ (4-Chlorophenyl) methyl]-9'- (4-morpholinylmethyl)-4, 7'- dioxospiro [cyclohexane-1, 2' (3'H)- [7H] pyrido [1, 2,3-de] [1, 4] benzoxazine]-6'- carboxamide (Formula M-8 of Chart M, where Ra, Rb=4-cyclohexanone) A mixture of 104 mg of compound M-8 of Example 50 (where Ra, Rb=cyclohexane- 4-ethylene ketal), 3 mL of acetone, 3 mL of THF, and 1 mL of 6N HC1 is stirred for 18 h, the partitioned between chloroform and aqueous NaHCO3. The organic phase is dried (Na2SO4) and concentrated under reduced pressure. Flash chromatography of the residue on silica gel using 2-3% methanol in dichloromethane affords 101 mg of the title compound as a white solid. Recrystallization from acetonitrile provides white needles, mp 249.5- 252.0 °C.

1H NMR (CDC13) 8 1.98,2.24,2.40,2.47,2.78,3.61,3.72,4.13,4.64,7.31,7.44,7.98, 8.66,10.42 ppm.

TLC Rf 0. 33 (5% methanol in dichloromethane).

IR (diffuse reflectance) 1717,1658,1608,1576,1550,1502,1412,1312,1296,1275,1192, 1145,1109,875,809 cni-I OAMS supporting ions at: ESI+ 536.2 HRMS (FAB) calcd for C29H30CLN3O5 +H1 536.1952, found 536.1951 Anal. Calcd for C29H30ClN305 : C, 64.98; H, 5.64; N, 7.84; Cl, 6.61; found: C, 64.85; H, 5.83; N, 7.85. Example 55: N- [ (4-Chlorophenyl) methyl]-4-hydroxy-9'- (4-morpholinylmethyl)-7'- oxospiro [cyclohexane-1, 2' (3'H)- [7H] pyrido [1, 2,3de] [1, 4] benzoxazine]-6'- carboxamide (Formula M-8 of Chart M, where Ra, Rb=4-cyclohexanol)

To a stirred solution of 118 mg of the produce of Example 54 in 2 mL of dichloromethane and 1 mL of methanol, cooled at 0 °C, is added 10 mg of sodium borohydride. After ten minutes, the reaction mixture is partitioned between water and dichloromethane, and the organic phase is dried (Na2SO4) and concentrated under reduced pressure. Flash chromatography of the residue on silica gel using 4-6% methanol in dichloromethane affords 69 mg of the title compound as a yellow solid. Recrystallization from acetonitrile provides pale yellow needles, mp 229-234 °C.

'H NMR (CDC13) 8 1.54,1.6-2.0,2.46,3.59,3.72,3.78,4.00,4.64,7.3,7.38,7.93,8.6 2, 10.47 ppm.

TLC Rf0. 29 (7% methanol in dichloromethane).

IR (diffuse reflectance) 1653,1607,1574,1552,1504,1411,1324,1281,1250,1240,1114, 1107,881,810,801 crn~l OAMS supporting ions at: ESI+ 538.3 Anal. Calcd for C29H32C1N305 : C, 64.74; H, 5.99; N, 7.81; Cl, 6.59; found: C, 64.63; H, 5.98; N, 7.79.

Example 56: N-(4-Chlorobenzyl)-2-{[(4-chlorobenzyl) amino] methyl}-9-(morpholin-4- ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (A-11 of Chart A, where R6 is 4-chlorobenzylamino) Following the procedure in Example 2, the title compound is obtained.

1H NMR (CDC13) 8 1.88,2.45,3.03,3.57,3.70,3.85,4.3,4.4,4.63,7.30,7.34,7.92,8. 63, 10.45 ppm.

IR (diffuse reflectance) 2858,1648,1627,1607,1570,1551,1536,1499,1451,1411,1330, 1283,1112,811, 800 cm-1.

OAMS supporting ions at: ESI+ 609.2 HRMS (FAB) calcd for C32H32CL2N404 +HI 607.1879, found 607.1872.

Anal. Calcd for C32H32C12N404 : C, 63.26; H, 5.31; N, 9.22; Cl, 11.67; found: C, 63.12; H, 5.29; N, 9.19.

Example 57: N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2- (R or S)-pyridin- 2-yl-2,3-dihydro-7H- [1,4] oxazino [2, 3,4-ij] quinoline-6-carboxamide (I-6 of Chart I, T=2- pyridyl) The enantiomers are prepared by resolution of racemic compound of Example 33 on chiral HPLC using a chiralcel OD column eluted with 0.025% diethylamine in ethanol, giving Isomer 1 (first eluting) and Isomer 2 (second eluting).

'H NMR (CDC13) 6 2.47,3.61,3.72,4.58,4.63,4.72,5.51,7.3,7.50,7.63,7.79,7.97,8 .63, 8.72,10.44 ppm.

OAMS supporting ions at: ESI+ 531.3.

Example 58: N- (4-Chlorobenzyl)-9- (morpholin-4-ylmethyl)-7-oxo-2- (R or S)-pyridin- 3-yl-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (I-6 of Chart I, T=3- pyridyl)

The enantiomers are prepared by resolution of racemic compound of Example 34 on chiral HPLC using a chiralcel OD column eluted with 0.1% diethylamine in ethanol, giving Isomer 1 (first eluting) and Isomer 2 (second eluting).

'H NMR (CDC13) 8 2.46,3.60,3.71,4.32,4.47,4.60,5.37,7.27,7.44,7.84,7.99,8.70, 8.72,8.79,10.41 ppm.

OAMS supporting ions at: ESI+ 531.2.

Example 59: N- (4-Chlorobenzyl)-2- (1-methyl-lH-imidazol-2-yl)-9- (morpholin-4- ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2, 3,4-ij] quinoline-6-carboxamide (I-6 of Chart I, T=1-methylimidazol-2-yl) Following the procedure in Preparations 37-41 and Example 33 without making major changes except using 1-methylimidazole-2-carboxaldehyde as the starting aldehyde, the title compound is obtained as a light brown solid. Recrystallization from acetonitrile gives tan granular crystals, mp >260 °C.

'H NMR (CDC13) 8 2.46,3.56,3.60,3.70,3.85,4.63,4.69,4.95,5.46,7.00,7.03,7.30, 7.38,7.97,8.75,10.43 ppm.

TLC Rf 0. 23 (5% methanol in dichloromethane).

IR (diffuse reflectance) 3047,2988,2851,1652,1627,1607,1569,1550,1500,1458,1411, 1347,1279,1119,810 cm~l OAMS supporting ions at: ESI+ 534.4 HRMS (FAB) calcd for C28H28CLN504 +Hl 534.1908, found 534.1913 Anal. Calcd for C28H28ClN504 : C, 62.98; H, 5.28; N, 13.11; Cl, 6.64; found: C, 63.06; H, 5.32; N, 13.11.

Example 60: N- (4-Chlorobenzyl)-2- (2-furyl)-9- (morpholin-4-ylmethyl)-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (I-6 of Chart I, T-2-furyl)

Following the procedure in Preparations 37-41 and Example 33 without making major changes except using furfural as the starting aldehyde, the title compound is obtained as a light yellow solid. Recrystallization from acetonitrile gives tan needles, mp 220.0- 222.5 °C.

IH NMR (CDC13) 8 2.45,3.58,3.69,4.48,4.61,4.63,5.44,6.44,6.50,7.30,7.41,7.50, 7.97,8.70,10.44 ppm.

TLC Rf 0. 31 (3% methanol in dichloromethane).

IR (diffuse reflectance) 1655,1627,1608,1551,1500,1411,1347,1330,1282,1225,1114, 1011,882,809,760 cm' OAMS supporting ions at: ESI+ 520.3 HRMS (FAB) calcd for C2SH26CLN305 +Hl 520.1639, found 520.1638.

Anal. Calcd for C28H26ClN305 : C, 64.68; H, 5.04; N, 8.08; Cl, 6.82; found: C, 64.47; H, 5.04; N, 8.08.

Preparation 49: {3-[(Methoxymethoxy) methyl] phenyl} methanol (N-2 of Chart N, where substitution is meta, n=l, and P=methoxymethyl) To a stirred, cooled (0 °C) solution of 6.91 g of 1,3-benzenedimethanol and 9.6 mL of diisopropylethylamine in 50 mL of dichloromethane is added 3.8 mL of chloromethyl methyl ether. After 90 min, 25 mL of 1N HC1 is added, the phases separated, and the aqueous extracted with two additional portions of dichloromethane. The combined organic phase is dried (Na2SO4) and concentrated under reduced pressure. Flash chromatography on silica using 40% ethyl acetate in dichloromethane affords 4.76 g of the monoprotected compound as a pale yellow liquid.

'H NMR (CDC13) 8 2.03,3.41,4.59,4.68,4.70,7.3 ppm.

TLC Rf 0. 36 (1: 1 ethyl acetate in dichloromethane, vanillin staining).

Preparation 50: 3- [ (Methoxymethoxy) methyl] benzaldehyde (N-3 of Chart N, where substitution is meta, n=1, and P=methoxymethyl)

To a well-stirred mixture of 10.8 g of PCC and 820 mg of sodium acetate in 20 mL of dichloromethane is added a solution of 1.82 g of alcohol of Preparation 49 in 10 mL of dichloromethane. After 18 h, silica gel is added and the mixture filtered through a short plug of silica gel, which is rinsed with 1: 1 ethyl acetate-dichloromethane. The filtrate is concentrated under reduced pressure, and the residue flash chromatographed on silica gel using 1: 1 ether-hexane to afford 1.61 g of the title aldehyde as a colorless liquid.

1H NMR (CDCl3) 8 3.43,4.68,4.74,7.53,7.64,7.82,7.89,10.03 ppm.

TLC Rf 0. 32 (1 : 1 ether-hexane).

Preparation 51: 2-Amino-1-{3-[(methoxymethoxy) methyl] phenyl} ethanol (N-5 of Chart N, where substitution is meta, n=l, and P=methoxymethyl) To a mixture of 1.58 g of aldehyde of Preparation 50 and 1.3 mL of TMSCN, stirred neat under argon, is added a catalytic amount (ca. 10 mg) of ZnI2. After 16 h, the resulting yellow liquid is dissolved in 15 mL of dry ether and added dropwise via cannula to a cooled (0 °C), mechanically stirred slurry of 370 mg of LAH in 20 mL of dry ether. Efficient stirring is required at this stage to assure complete reaction and reasonable product yield.

Following the cyanohydrin addition, the reaction mixture is allowed to warm to ambient temperature and stirred vigorously for 2 h. The mixture is then recooled to 0 °C and quenched cautiously with 0.37 mL of water in 10 mL of THF, 0.37 mL of 3N NaOH, and 1.0 mL of water. Sodium sulfate and dichloromethane were added, and the mixture stirred well for 30-90 minutes, then filtered. The filter cake is washed well with ether- dichloromethane and then concentrated under reduced pressure to afford 2.08 g of the amino alcohol as a yellow oil.

'H NMR (CDC13) 8 2.2,2.81,2.99,3.42,4.60,4.6,4.71,7.3 ppm.

OAMS supporting ions at: ESI+ 212.1 Preparation 52: Ethyl 2-(2, 3-difluoro-5-iodobenzoyl)-3-[(2-hydroxy-2-{3- [ (methoxymethoxy) methyl] phenyl} ethyl) amino] prop-2-enoate (N-6 of Chart N, where substitution is meta, n= 1, and P=methoxymethyl) To a stirred solution of 5.0 mmol of compound I-1 (prepared as described in Preparation 38) in 15 mL of ethanol is added 2.0 g of crude amino alcohol of Preparation 51. The solution is stirred for 18 h, then concentrated under reduced pressure. Flash

chromatography of the residue on silica using 10-20% ethyl acetate in dichloromethane provides 2.31 g of the title compound as an yellow foam.

'H NMR (CDC13) is complex due to EIZ isomers : 8 0.90,1.02,3.3,3.6,4.0,4.58,4.69, 4.85,7.3,8. 1 ppm.

TLC Rf 0. 20 (10% ethyl acetate in dichloromethane).

OAMS supporting ions at: ESI+ 576.2.

Preparation 53: Ethyl 9-iodo-2- {3- [ (methoxymethoxy) methyl] phenyl}-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxylate (N-7 of Chart N, where substitution is meta, n=l, and P=methoxymethyl) A mixture of 2.3 g of compound N-6 of Preparation 52 and 2.9 g of cesium carbonate in 8 mL of DMF is stirred at 100 °C under argon for 18 h, then cooled and partitioned between dichloromethane and dilute HC1. The organic phase is dried (Na2S04) and concentrated under reduced pressure. Flash chromatography on silica gel using 2% methanol in dichloromethane provides 1.60 g of the title compound as a brown solid.

Recrystallization from acetonitrile affords tan crystals, mp 153.3-156.0 °C.

'H NMR (CDC13) 8 1.37,3.44,4.27,4.32,4.66,4.75,5.38,7.5,7.57,8.22,8.26 ppm.

TLC Rf 0. 47 (5% methanol in dichloromethane).

IR (diffuse reflectance) 1680,1632,1610,1586,1550,1496,1316,1257,1224,1182,1148, 1113,1048,921,799 cm- ; OAMS supporting ions at: ESI+ 536.1; HRMS (FAB) calcd for C23H22lNO6 +Hl 536. 0572, found 536.0587; Anal. Calcd for C23H22IN06 : C, 51.60; H, 4.14; N, 2.62; found: C, 51.40; H, 4.25; N, 2.50.

Preparation 54: Ethyl 9-formyl-2- {3- [ (methoxymethoxy) methyl] phenyl}-7-oxo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxylate (N-8 of Chart N, where substitution is meta, n=l, and P=methoxymethyl) A mixture of 1.46 g of iodide N-7 of Preparation 53 and 220 mg of tetrakis (triphenylphosphine) palladium (0) in 15 mL of dry DMF is purged with CO, via a needle reaching to the bottom of the flask, and heated to 55 °C. To the stirred mixture is added, via syringe pump, 1.0 mL of tributyltin hydride in 9 mL of dry THF. Bubbling of CO through the mixture is continued throughout the addition, which took about 5 h. The mixture is then cooled and concentrated under reduced pressure. Flash chromatography of

the residue on silica gel using 2% methanol in dichloromethane affords 970 mg of the title compound as a tan solid.

'H NMR (CDC13) 8 1.41,3.44,4. 33,4.40,4.67,4.75,5.36,7.5,7.80,8.36,8.54,10.06 ppm.

TLC Rf 0. 31 (3% methanol in dichloromethane).

OAMS supporting ions at: ESI+ 438. 2.

Preparation 55: Ethyl 2- {3- [ (methoxymethoxy) methyl] phenyl}-9- (morpholin-4- ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxylate (N-9 of Chart N, where substitution is meta, n=1, and P=methoxymethyl) To a mixture of 0.97 g of aldehyde of Preparation 54,0.58 mL of morpholine, and 0.25 mL of acetic acid in 20 mL of THF is added 940 mg of sodium triacetoxyborohydride.

After 4 h, additional borohydride (300 mg) is added, and the mixture is stirred for 2 h and then partitioned between dichloromethane and aqueous NaHCO3. The organic phase is dried (Na2S04) and concentrated under reduced pressure. Flash chromatography of the residue on silica using 3-4% methanol in dichloromethane provides 940 mg of the title compound as a grey solid. Recrystallization from ethyl acetate gave white needles, mp 148- 153 °C.

'H NMR (CDC13) 8 1. 37,2.45,3.44,3.55,3.69,4.24,4.3,4. 33,4.67,4.75,5.36,7.36,7.47, 7.55,7.93,8.26 ppm.

TLC Rf 0. 30 (5% methanol in dichloromethane).

IR (diffuse reflectance) 2953,1686,1638,1608,1555,1506,1322,1291,1271,1221,1183, 1148,1115,1041,796 ciifl ; OAMS supporting ions at: ESI+ 509.4; HRMS (FAB) calcd for C28H32N207 +Hl 509.2288, found 509.2285; Anal. Calcd for C2sH32N207 : C, 66.13; H, 6.34; N, 5.51; found: C, 66.15; H, 6.41; N, 5.43.

Example 61: N- (4-Chlorobenzyl)-2- {3- [ (methoxymethoxy) methyl] phenyl}-9- (morpholin-4-ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide (N-10 of Chart N, where substitution is meta, n=l, and P=methoxymethyl)

A mixture of 780 mg of ester of Preparation 55 and 1.3 g of p-chlorobenzylamine is stirred neat at 150 °C for 18 h, then concentrated in vacuo. Flash chromatography of the residue on silica using 2% methanol in dichloromethane provides 790 mg of the title compound as a white solid. Recrystallization from acetonitrile-methanol affords fine white needles, mp 186.5-189.0 °C.

'H NMR (CDC13) 8 2.46,3.43,3.59,3.70,4.30,4.41,4.60,4.65,4.74,5.30,7.27,7.44, 7.52,7.97,8.68,10.44 ppm.

TLC Rf 0. 29 (3% methanol in dichloromethane).

IR (diffuse reflectance) 1649,1607,1552,1501,1411,1350,1284,1270,1223,1147,1115, 1092,1047,810,799 cm 1 ; OAMS supporting ions at: ESI+ 604.3; HRMS (FAB) calcd for C33H34CLN306 +Hl 604.2214, found 604.2225; Anal. Calcd for C33H34ClN306 : C, 65.61; H, 5.67; N, 6.96; Cl, 5.87; found: C, 65.57; H, 5.72; N, 6.90.

Example 62: N- (4-Chlorobenzyl)-2- [3- (hydroxymethyl) phenyl]-9- (morpholin-4- ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (N-11 of Chart N, where substitution is meta, n=1, and P=methoxymethyl) A solution of 122 mg of N-10 of Example 61 in 1 mL of ethanol and 0.5 mL of conc. HC1 is stirred for 36 h at room temperature, then added to stirred aqueous NaHC03.

The resulting solid is filtered, washed well with water, dried under vacuum, and then absorbed onto silica gel. Flash chromatography on silica gel using 3-5% methanol in dichloromethane provides 108 mg of the title compound as a white solid. Recrystallization from acetonitrile-methanol provides material with mp 229-233 °C.

'H NMR (CDC13+CD30D) 5 2.49,3.62,3.72,4.30,4.49,4.62,4.72,5.32,7.30,7.43,7.54, 7.95,8.63,10.58 ppm.

TLC Rf 0. 25 (5% methanol in dichloromethane).

IR (diffuse reflectance) 1653,1606,1570,1549,1542,1499,1409,1325,1292,1277,1219, 1114,1077,807,800 cm 1 ; OAMS supporting ions at: ESI+ 560.3; HRMS (FAB) calcd for C31H30CLN305 +Hl 560.1952, found 560.1945; Anal. Calcd for C3lH30ClN3Os : C, 66.48; H, 5.40; N, 7.50; Cl, 6.33; found (av): C, 64.94; H, 5. 33 ; N, 7.29.

Preparation 56: 3-{[tert-Butyl (dimethyl) silyl] oxy} benzaldehyde (N-3 of Chart N, where substitution is meta, n=0, and P=tert-butyldimethylsilyl) A solution of 3.66 g of 3-hydroxybenzaldehyde, 3.1 g of imidazole, and 4.39 g of tert-butyldimethylsilyl chloride in 10 ml of DMF is stirred at room temperature for 18 h, then partitioned between ether and water. The organic phase is washed with water, dried (MgS04), and concentrated under reduced pressure. Flash chromatography of the residue on silica gel using 5% ether-hexane provides 5.14 g of the title compound as a pale yellow liquid.

'H NMR (CDCl3) 0.22,1.00,7.11,7.33,7.40,7.48,9.96 ppm.

TLC Rf0. 28 (5% ether-hexane).

OAMS supporting ions at: ESI+ 237.1.

Preparation 57: 2-Amino-1-(3-{[tert-butyl (dimethyl) silyl] oxy} phenyl) ethanol (N-5 of Chart N, where substitution is meta, n=0, and P=tert-butyldimethylsilyl) The procedure described in Preparation 51 is followed starting with 5.14 g of the product of Preparation 56 to provide 6.96 g of crude amino alcohol as an amber oil.

IH NMR (CDC13) 8 0.19,0.98,2.1,2.79,2.97,4.59,6.74,6.85,6.93,7.19 ppm.

OAMS supporting ions at: ESI+ 268.3.

Preparation 58: Ethyl 3-1 [2- (3-1 [tert-butyl (dimethyl) silyl] oxy} phenyl)-2- hydroxyethyl] amino}-2-(2,3-difluoro-5-iodobenzoyl) prop-2-enoate (N-6 of Chart N, where substitution is meta, n=0, and P=tert-butyldimethylsilyl)

The procedure described in Preparation 52 is followed starting with 5.14 g of the product of Preparation 57. Flash chromatography on silica using 30% ethyl acetate in hexane affords 4.11 g of the title compound as a yellow foam.

'H NMR (CDCl3) is complex due to E/Z isomers : 8 0.20,0.99,1.04,2.6,3.6,4.0,4.8,6.8, 6.9,7.2,7.4,8.1,9.68,11.03 ppm.

TLC Rf 0. 28 (30% ethyl acetate-hexane).

OAMS supporting ions at: ESI+ 632.2.

Preparation 59: Ethyl 2-(3-{[tert-butyl (dimethyl) silyl] oxy} phenyl)-9-iodo-7-oXo-2, 3- dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxylate (N-7 of Chart N, where substitution is meta, n=0, and P=tert-butyldimethylsilyl) A mixture of 3.44 g of the product of Preparation 58 and 3.9 g of cesium carbonate in 10 ml of DMF is stirred and heated at 100 °C under argon for 18 h, then cooled. Acetic acid (1 ml) is added, followed by 75 ml of water, and dilute HCl is added to bring the pH to about 2. The resulting solid is filtered, washed well with water, and dried in vacuo to provide 2.53 g of insoluble yellow-tan solid. To a mixture of this solid and 723 mg of imidazole in 6 ml of DMF is added 1.20 g of tert-butyldimethylsilyl chloride. The solution is stirred overnight, then partitioned between ethyl acetate and water. The organic phase is washed with water and brine, dried (MgS04), and concentrated under reduced pressure.

Flash chromatography on silica using 20-30% ethyl acetate in dichloromethane provides 2.15 g of the title compound as a tan solid. Recrystallization from acetonitrile provides an analytical sample; mp 227.0-228.5 °C.

'H NMR (CDC13) 8 0.23,1.00,1.36,4.25,4.30,5.34,6.91,6.99,7.11,7.34,7.56,8.19, 8.21 ppm.

TLC Rf 0. 36 (20% ethyl acetate in dichloromethane).

IR (diffuse reflectance) 1679,1630,1609,1586,1549,1493,1369,1319,1291,1251,878, 865,840,803,786 cm~l ; OAMS supporting ions at: ESI+ 592.3; HRMS (FAB) calcd for C26H30IN05SI +Hl 592.1018, found 592.1013; Anal. Calcd for C26H30IN05Si : C, 52.79; H, 5.11; N, 2. 37 ; found: C, 52.57; H, 5.15; N, 2. 34.

Preparation 60: Ethyl 2- (3- { [tert-butyl (dimethyl) silyl] oxy} phenyl)-9-formyl-7-oxo-2, 3- dihydro-7H- [l, 4] oxazino [2,3,4-ij] quinoline-6-carboxylate (N-8 of Chart N, where substitution is meta, n=0, and P=tert-butyldimethylsilyl) A mixture of 592 mg of the product of Preparation 59 and 81 mg of tetrakis (triphenylphosphine) palladium (0) in 5 ml of dry THF is purged with CO, via a needle reaching to the bottom of the flask, and heated to 50 °C. To the stirred mixture is added, via syringe pump, 0.35 ml of tributyltin hydride in 10 ml of dry THF. Bubbling of CO through the mixture is continued throughout the addition, which takes about 5 h. The mixture is then cooled and concentrated under reduced pressure. Flash chromatography of the residue on silica gel using 1-2% methanol in dichloromethane affords 625 mg of tan solid. This is triturated with ether-hexane, filtered, washed well with hexane, and dried in vacuo to provide 443 mg of the aldehyde as a tan solid. Recrystallization from acetonitrile affords white needles, mp 246-248 °C.

'H NMR (CDC13) 8 0.22,0.99,1.41,4.3,4.39,5.31,6.9,7.07,7.35,7.80,8.36,8.52,10 .05 ppm.

TLC Rf 0. 31 (2% methanol in dichloromethane).

Summary Analytical data for: 0071676; nbk# 35116-SRT-37A: IR (diffuse reflectance) 1727,1679,1646,1603,1556,1501,1373,1288,1258,899,877, 861, 840, 804,787 cni-i ; OAMS supporting ions at: ESI+ 494.3; HRMS (FAB) calcd for C27H3lNO6SI +Hl 494.1999, found 494.2005; Anal. Calcd for C27H3lNO6Si : C, 65.69; H, 6.33; N, 2.84; found: C, 65.73; H, 6.41; N, 2.93 Preparation 61: Ethyl 2- (3-1 [tert-butyl (dimethyl) silyl] oxy} phenyl)-9- (4- morpholinylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxylate (N-9 of Chart N, where substitution is meta, n=0, and P=tert- butyldimethylsilyl) To a mixture of 217 mg of the product of Preparation 60,0.12 ml of morpholine, and 50 gel of acetic acid in 4 ml of THF is added 140 mg of sodium triacetoxyborohydride.

After 18 h, additional borohydride (120 mg) is added, and the mixture is stirred for 2 h and then partitioned between dichloromethane and aqueous NaHCO3. The organic phase is dried (Na2SO4) and concentrated under reduced pressure. Flash chromatography of the

residue on silica using 3% methanol in dichloromethane provides 200 mg of the product as a white solid. Recrystallization from acetonitrile gives white crystals, mp 161-164 °C.

'H NMR (CDC13) 5 0.23,1.00,1. 39,2.46,3.57,3.70,4.22,4.30,4.35,5.27,6.91,6.98, 7.10,7. 34,7.38,7.96,8.29 ppm.

TLC Rf 0. 33 (5% methanol in dichloromethane).

IR (diffuse reflectance) 2955,2931,1725,1692,1607,1555,1503,1287,1261,1253,1222, 1115,878,863,840 cm~l ; OAMS supporting ions at: ESI+ 565.4; HRMS (FAB) calcd for C3lH4oN206SI +Hl 565.2734, found 565.2740; Anal. Calcd for C31H40N206Si : C, 65.93; H, 7.14; N, 4.96; found (av): C, 65.35; H, 7.16; N, 4.88.

Preparation 62 : 2-(3 {[tert-BIltyl (dimethyl) silyl] oxy} phenyl)-N- (4-chlorobenzyl)-9- (4- morpholinylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide (N-10 of Chart N, where substitution is meta, n=0, and P=tert- butyldimethylsilyl) A mixture of 341 mg of the product of Preparation 61 and 0.70 g of p- chlorobenzylamine is stirred neat at 150 °C for 18 h, then concentrated in vacuo. Flash chromatography of the residue on silica using 2-6% methanol in dichloromethane provides 233 mg of the title compound as a tan solid, as well as 130 mg of desilylated material.

Recrystallization of the main product from acetonitrile gives yellow prisms, mp 174-180 °C.

'H NMR (CDC13) 8 0.22,1.00,2.48,3.61,3.71,4.27,4.37,4.63,5.25,6.92,6.96,7.06, 7.30,7.34,7.47,7.98,8.66,10.45 ppm.

TLC Rf0. 29 (3% methanol in dichloromethane).

IR (diffuse reflectance) 1655,1607,1569,1551,1499,1411,1281,1262,1114,882,863, 840,809,798,782 cm-1; OAMS supporting ions at: ESI+ 660.5; HRMS (FAB) calcd for C36H42CLN30sSI +Hl 660.2660, found 660.2632; Anal. Calcd for C36H42ClN3O5Si : C, 65.49; H, 6.41; N, 6.36; Cl, 5.37; found: C, 65.42; H, 6.36; N, 6.36.

Example 63: N- (4-Chlorobenzyl)-2- (3-hydroxyphenyl)-9- (4-morphounylmethyl)-7- oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide (N-11 of Chart N, where substitution is meta, n=0, and P=tert-butyldimethylsilyl)

A solution of 167 mg of the product of Preparation 62 in 4 ml of ethanol and 2 ml of conc. HC1 is stirred for 18 h at room temperature, then added to a stirred solution of 2 g NaHCO3 in 50 ml of water. The resulting solid is filtered, washed well with water, dried under vacuum, and then absorbed onto silica gel. Flash chromatography on silica using 3- 5% methanol in dichloromethane provides 126 mg of the title compound as a white solid.

Recrystallization from acetonitrile gives glistening prisms, mp 213 °C (d). lH NMR (CDC13+CD30D) 6 2.49,3.62,3.72,4.29,4.48,4.63,5.25,6.89,6.97,7.30,7.44, 7.94,8.62,10.61 ppm.

TLC Rf 0. 35 (5% methanol in dichloromethane).

Summary Analytical data for: 0071891; nbk# 35116-SRT-53A: IR (diffuse reflectance) 3059,2864,2843,1655,1608,1586,1569,1550,1531,1499,1408, 1335,1286,1278,1120cm~l, OAMS supporting ions at: ESI+ 546.3; HRMS (FAB) calcd for C3oH28CLN305 +Hl 546.1796, found 546.1781; Anal. Calcd for C3oH28ClN3Os : C, 65.99; H, 5.17; N, 7.70; Cl, 6.49; found: C, 65.57; H, 5.27; N, 8.57.

Example 64: N- (4-Chlorobenzyl)-2- [2- (methoxymethoxy) phenyl]-9- (morpholin-4- ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (I-6 of Chart I, T=2-methoxymethoxyphenyl)

Following the procedures in Preparations 49 and 51-55 and Example 61 without making major changes except using 2-hydroxybenzaldehyde as the starting aldehyde, the title compound is obtained as a white solid. Recrystallization from acetonitrile gives 324 mg of white solid.

'H NMR (CDC13) 8 2.47,3.49,3,61,3.71,4.15,4.50,4.63,4.64,5.25,5.29,5.65,7. 15,7.3, 7.39,7.47,7.61,7.98,8.68,10.49 ppm.

TLC Rf 0. 34 (3% methanol in dichloromethane).

OAMS supporting ions at: ESI+ 590.3.

Example 65: N- (4-Chlorobenzyl)-2- (4-hydroxyphenyl)-9- (morpholin-4-ylmethyl)-7- oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6-carboxamide (I-6 of Chart I, T=4- hydroxyphenyl) Following the procedures in Preparations 56,51-52, and 59-62 and Example 63 without making major changes except using 4-hydroxybenzaldehyde as the starting aldehyde, the title compound is obtained as a beige solid. Recrystallization from acetonitrile gives pale yellow crystals, mp >260 °C : 'H NMR (CDC13 + CD30D) 8 2.49,3.63,3.72,4.33,4.47,4.64,5.24,6.93,7.31,7.34,7.44, 7.95,8.65,10.62 ppm.

TLC Rf 0. 35 (5% methanol in dichloromethane).

IR (diffuse reflectance) 3035,1654,1608,1554,1518,1500,1410,1298,1284,1270,1253, 1230,1115,809,797 crn~l OAMS supporting ions at: ESI+ 546.3 HRMS (FAB) calcd for C3oH28CLN305 +Hl 546.1796, found 546.1793 Anal. Calcd for CsoHzgCOs : C, 65. 99; H, 5.17; N, 7.70; Cl, 6.49; found (av): C, 65.37; H, 5.19; N, 7.60.

Example 66: N-(4-Chlorobenzyl)-2-{2-[(methoxymethoxy) methyl] phenyl}-9- (morpholin-4-ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide (I-6 of Chart I, T=2-methoxymethoxymethylphenyl)

Following the procedures in Preparations 49-55 and Example 61 without making major changes except using 1,2-benzenedimethanol as the starting alcohol, the title compound is obtained as a white solid. Recrystallization from acetonitrile-methanol affords white crystals, mp 202.5-204.5 °C.

'H NMR (CDC13) b 2.48,3.32,3.62,3.71,4.23,4.52,4.6-4.7,4.77,5.57,7.30,7.4,7.5 , 7.66,7.99,8.64,10.47 ppm.

TLC Rf 0.30 (3% methanol in dichloromethane).

IR (diffuse reflectance) 1652,1607,1569,1552,1500,1410,1352,1283,1228,1150,1116, 1092,1034,810, 748cm'' OAMS supporting ions at: ESI+ 604.3 HRMS (FAB) calcd for C33H34CLN306 +Hl 604.2214, found 604.2215 Anal. Calcd for C33H34C1N306 : C, 65.61; H, 5.67; N, 6.96; Cl, 5.87; found: C, 65.40; H, 5.69; N, 6.95.

Example 67: N- (4-Chlorobenzyl)-2- {4- [ (methoxymethoxy) methyl] phenyl}-9- (morpholin-4-ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2,3,4-ij] quinoline-6- carboxamide (I-6 of Chart I, T=4-methoxymethoxymethylphenyl) Following the procedures in Preparations 49-55 and Example 61 without making major changes except using 1,4-benzenedimethanol as the starting alcohol, the title

compound is obtained as a tan solid. Recrystallization from acetonitrile-methanol affords tan crystals, mp 236-239 °C.

'H NMR (CDC13) 8 2.47,3.44,3.60,3.70,4.29,4.37,4.63,4.65,4.74,5. 31,7.3,7.45,7.49, 7.98,8.67,10.44 ppm.

TLC Rf 0. 27 (3% methanol in dichloromethane).

IR (diffuse reflectance) 2931,2852,1653,1607,1569,1551,1536,1500,1411,1328,1280, 1149,1113,1044,809 cm' OAMS supporting ions at: ESI+ 604. 3 HRMS (FAB) calcd for C33H34CLN306 +Hl 604.2214, found 604.2219 Anal. Calcd for C33H34CIN306 : C, 65.61; H, 5.67; N, 6.96; Cl, 5.87; found: C, 65.49; H, 5.73; N, 6.90.

Example 68: N- (4-Chlorobenzyl)-2- (2-hydroxyphenyl)-9- (morpholin-4-ylmethyl)-7- oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxamide (I-6 of Chart I, T=2- hydroxyphenyl) Following the procedure in Example 62 using the compound of Example 64 as the starting material, the title compound is obtained as a white solid. Trituration with hot acetonitrile affords an analytical sample; mp-239 °C.

'H NMR (CDC13) 8 2.48,3.61,3.71,4.09,4.62,4.68,5.63,6.88,6.97,7.17,7.3,7.49,7 .52, 7.97,8.57,9.5,10.86 ppm.

TLC Rf 0. 31 (5% methanol in dichloromethane).

IR (diffuse reflectance) 3162,1645,1603,1568,1550,1499,1457,1411,1353,1331,1300, 1282,1272,1221,809 cm~l OAMS supporting ions at: ESI+ 545.9 HRMS (FAB) calcd for C30H28CLN3O5 +H1 546.1796, found 546.1796 Anal. Calcd for C3oH2gClN3O5 : C, 65.99; H, 5.17; N, 7.70; Cl, 6.49; found: C, 65.89; H, 5.23; N, 7.59.

Example 69: N- (4-Chlorobenzyl)-2- [2- (hydroxymethyl) phenyl]-9- (morpholin-4- ylmethyl)-7-oxo-2, 3-dihydro-7H- [1, 4] oxazino [2, 3,4-ij] quinoline-6-carboxamide (I-6 of Chart I, T=2-hydroxymethylphenyl)

Following the procedure in Example 62 using the compound of Example 66 as the starting material, the title compound is obtained as a white solid. Recrystallization from acetonitrile gives white crystals, mp 218-223 °C (d).

'H NMR (CDC13+CD30D) 6 2.50,3.65,3.73,4.24,4.63,4.67,4.72,4.83,5.69,7.3,7.4- 7.5,7.65,7.96,8.59,10.62 ppm.

TLC Rf 0. 32 (5% methanol in dichloromethane).

IR (diffuse reflectance) 3406,2863,1670,1609,1569,1551,1500,1410,1349,1330,1285, 1105,808,798, 752 cm-1 OAMS supporting ions at: ESI+ 560.3 HRMS (FAB) calcd for C3lH30CLN305 +Hl 560.1952, found 560.1947 Anal. Calcd for C3lH30ClN305 : C, 66.48; H, 5.40; N, 7.50; Cl, 6.33; found: C, 66.11; H, 5.42; N, 7.47.