789, 1 0-Tetrahydro-6H-azeninoN 678, 9-tetrahvdro-<BR> <BR> pvrido and 2, 3-dihydro-2H-pyrrolof2, 1-bl- auinazolinone derivatives The present invention relates to novel 7,8, 9, 10-tetrahydro-6H-azepino, 6,7, 8, 9-tetrahydro- pyrido and 2, 3-dihydro-2H-pyrrolo [2, 1-b]-quinazolinone derivatives of the general formula I and their use as pharmaceuticals. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more compounds of formula I, and especially their use as orexin receptor antagonists.

The orexins (hypocretins) comprise two neuropeptides produced in the hypothalamus: the orexin A (OX-A) (a 33 aminoacid peptide) and the orexin B (OX-B) (a 28 aminoacid peptide) (Sakurai T. et al., Cell, 1998,92, 573-585). Orexins are found to stimulate food consumption in rats suggesting a physiological role for these peptides as mediators in the central feedback mechanism that regulates feeding behavior (Sakurai T. et al., Cell, 1998, 92,573-585). On the other hand, it was also proposed that orexins regulate states of sleep and wakefulness opening potentially novel therapeutic approaches for narcoleptic patients (Chemelli R. M. et al., Cell, 1999,98, 437-451). Two orexin receptors have been cloned and characterized in mammals. They belong to the superfamily of G-protein coupled receptor (Sakurai T. et al., Cell, 1998,92, 573-585): the orexin-1 receptor (OXl) is selective for OX-A and the orexin-2 receptor (OX2) is capable to bind OX-A as well as OX-B.

Orexin receptors are found in the mammalian host and may be responsible for many biological functions such as pathologies including, but not limited to, depression; anxiety; addictions; obsessive compulsive disorder; affective neurosis; depressive neurosis; anxiety neurosis; dysthymic disorder; behaviour disorder; mood disorder; sexual dysfunction; psychosexual dysfunction; sex disorder; schizophrenia; manic depression; delerium; dementia ; severe mental retardation and dyskinesias such as Huntington's disease and Tourette syndrome; feeding disorders such as anorexia, bulimia, cachexia and obesity; diabetes; appetite/taste disorders ; vomiting/nausea; asthma; cancer; Parkinson's disease ; Cushing's syndrome/disease; basophil adenoma; prolactinoma;

hyperprolactinemia; hypopituitarism; hypophysis tumor/adenoma; hypothalamic diseases; inflammatory bowel disease; gastric diskinesia; gastric ulcus; Froehlich's syndrome; adrenohypophysis disease; hypophysis disease ;, pituitary growth hormone ; adrenohypophysis hypofunction; adrenohypophysis hyperfunction; hypothalamic hypogonadism; Kallman's syndrome (anosmia, hyposmia); functional or psychogenic amenorrhea ; hypopituitarism; hypothalamic hypothyroidism; hypothalamic-adrenal dysfunction; idiopathic hyperprolactinemia; hypothalamic disorders of growth hormone deficiency; idiopathic growth deficiency; dwarfism; gigantism; acromegaly; disturbed biological and circadian rhythms; sleep disturbances associated with deseases such as neurological disorders, neuropathic pain and restless leg syndrome; heat and lung diseases, acute and congestive heart failure; hypotension; hypertension; urinary retention; osteoporosis; angina pectoris; myocardinal infarction; ischaemic or haemorrhagic stroke; subarachnoid haemorrhage; ulcers; allergies; benign prostatic hypertrophy; chronic renal failure; renal disease; impaired glucose tolerance; migraine; hyperalgesia; pain; enhanced or exaggerated sensitivity to pain such as hyperalgesia, causalgia, and allodynia; acute pain; burn pain; atypical facial pain; neuropathic pain; back pain; complex regional pain syndrome I and II; arthritic pain; sports injury pain; pain related to infection e. g. HIV, post-chemotherapy pain; post-stroke pain; post-operative pain; neuralgia; conditions associated with visceral pain such as irritable bowel syndrome, migraine and angina; urinary bladder incontinence e. g. urge incontinence; tolerance to narcotics or withdrawal from narcotics; sleep disorders; sleep apnea; narcolepsy; insomnia ; parasomnia; jet-lag syndrome; and neurodegerative disorders including nosological entities such as disinhibition-dementia-parkinsonism-amyotrophy complex; pallido-ponto-nigral degeneration epilepsy; seizure disorders and other diseases related to orexin.

The present invention provides 7, 8, 9, 10-tetrahydro-6H-azepino, 6,7, 8, 9- tetrahydro-pyrido and 2, 3-dihydro-2H-pyrrolo [2, 1-b]-quinazolinone derivatives which are non-peptide antagonists of human orexin receptors. In particular, these compounds are of potential use in the treatment of obesity and/or sleep disorders.

International Patent Applications W0099/09024, W0099/58533, WO00/47577, WO00/47580, disclose phenyl urea derivatives and WO00/47576, discloses quinolinyl cinnamide derivatives as orexin antagonists.

Furthermore, WO 0196302 has been published wherein piperidine derivatives as OXI and OX2 antagonists are disclosed and WO 0185693 has been published wherein N-

acyltetrahydroisoquinoline derivatives as selective OX2 antagonists are disclosed. In addition, WO 0244172 describes morpholine derivatives as antagonists of orexin receptors.

The novel compounds of the present invention belong to an entirely different class of low molecular weight compounds as compared to all prior art orexin receptor antagonists so far published.

The present invention relates to novel 7,8, 9, 10-tetrahydro-6H-azepino, 6,7, 8, 9- tetrahydro-pyrido and 2, 3-dihydro-2H-pyrrolo [2, 1-b]-quinazolinone derivatives of the general formula (I).

Formula (I) wherein: X is O or S; n is the integer 1,2, or 3; m is the integer 0,1, 2,3 ; Rl, R2, R3, R4 independently represent cyano, nitro, halogen, hydrogen, hydroxy, lower alkyl, lower alkenyl, lower alkoxy, lower alkenyloxy, trifluoromethyl, trifluoromethoxy, cycloalkyloxy, aryloxy, aralkyloxy, heterocyclyloxy, heterocyclyl-lower alkyloxy, R8CO-, NR9R10CO-,R9R10N-,R8OOC-,R8SO2NH-, Rll-CO-NEt-or R2 and R3 together or R1 and R2 together or R3 and R4 together

may form with the phenyl ring a five, six or seven-membered ring containing one or two oxygen atoms which are separated by at least one carbon atom; Rs represents aryl, aralkyl, lower alkyl, cycloalkyl, cycloalkyl-lower alkyl, heterocyclyl or heterocyclyl-lower alkyl ; R6 represents hydrogen, lower alkyl, trifluoromethyl,-(CH2) m-0Hp-(CH2) m-O-lower alkyl,- (CH2) m-C02H,- (CH2) m-C02-lower alkyl,- (CH2) mCONH2, or- (CH2) m-CONH-lower alkyl, or-(CH2) m-CON-(lower alkyl) 2, or- (CH2) m-N- (lower alkyl) 2; R7 represents aryl, aralkyl, lower alkyl, lower alkenyl, cycloalkyl, cycloalkyl-lower alkyl, heterocyclyl or heterocyclyl-lower alkyl ; R8 represents lower alkyl, aryl, aralkyl, heterocyclyl or heterocyclyl-lower alkyl ; R9and Rl° independently represent hydrogen, alkyl, cycloalkyl, cycloalkyl-loweralkyl, aryl, aralkyl, heterocyclyl or heterocyclyl-lower alkyl ; Rl l represents alkyl, aryl, cycloalkyl, heterocyclyl, RR"N-or R 80_.

The compounds of formula I can contain one or more asymmetric centres and can be present in the form of optically pure enantiomers, mixtures of enantiomers such as, for example, racemates, optically pure diastereoisomers, mixtures of diastereoisomers, diastereoisomeric racemates, mixture of diastereoisomeric racemates, or meso forms and pharmaceutically acceptable salts thereof.

In the present description the term"lower alkyl", alone or in combination, signifies a straight-chain or branched-chain alkyl group with 1 to 8 carbon atoms, preferably a straight or branched-chain alkyl group with 1-5 carbon atoms. Examples of straight-chain and branched Cl-C8 alkyl groups are methyl, ethyl, n-propyl, isopropyl, n-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, isobutyl, tert-butyl, the isomeric pentyl, the isomeric hexyls, the isomeric heptyls and the isomeric octyls, preferably methyl, ethyl, n- propyl, isopropyl, n-butyl, 2-butyl, tert-butyl and n-pentyl.

The term"lower alkenyl", alone or in combination, signifies a straight-chain or branched-chain alkenyl group with 2 to 5 carbon atoms, preferably allyl and vinyl.

The term"lower alkoxy", alone or in combination, signifies a group of the formula alkyl-O-in which the term"alkyl"has the previously given significance, such as methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, sec-butoxy and tert-

butoxy, preferably methoxy and ethoxy.

Lower alkenyloxy groups are preferably vinyloxy and allyloxy.

The term"cycloalkyl", alone or in combination, signifies a cycloalkyl ring with 3 to 8 carbon atoms and preferably a cycloalkyl ring with 3 to 6 carbon atoms.

Examples of C3-C8 cycloalkyl are cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl, preferably cyclopropyl, cyclohexyl or lower alkyl substituted cycloalkyl which may preferably be substituted with lower alkyl such as methyl- cyclopropyl, dimethyl-cyclopropyl, methyl-cyclobutyl, methyl-cyclopentyl, methyl- cyclohexyl, dimethyl-cyclohexyl, The term"aryl", alone or in combination, signifies a phenyl or naphthyl group which optionally carries one or more substituents, preferably one or two substituents, each independently selected from cyano, halogen, hydroxy, lower alkyl, lower alkenyl, lower alkoxy, lower alkenyloxy, nitro, trifluoromethyl, trifluoromethoxy, amino, carboxy, alkoxycarbonyl and the like, such as phenyl, p-tolyl, 4-methoxyphenyl, 4-tert- butoxyphenyl, 4-fluorophenyl, 2-chlorophenyl, 4-hydroxyphenyl, 1-naphthyl and 2- naphthyl. Preferred are carboxyphenyl, lower alkoxy-phenyl, hydroxyphenyl and particularly phenyl.

The term"aralkyl", alone or in combination, signifies an alkyl or cycloalkyl group as previously defined in which one hydrogen atom has been replaced by an aryl group as previously defined. Preferred are benzyl and benzyl substituted in the phenyl ring with hydroxy, lower alkyl, lower alkoxy or halogen preferably fluorine.

Particularly preferred is benzyl.

For the term"heterocyclyl"and"heterocyclyl-lower alkyl", the heterocyclyl group is preferably a 5-to 10-membered monocyclic or bicyclic ring, which may be saturated, partially unsaturated or aromatic containing for example 1,2 or 3 heteroatoms selected from oxygen, nitrogen and sulphur which may be the same or different. Example of such heterocyclyl groups are pyrrolidinyl, piperidinyl, piperazinyl, morpholinyl, pyridyl, pyrimidinyl, pyrazinyl, pyridazinyl, quinolyl, isoquinolyl, thienyl, thiazolyl, isothiazolyl, furyl, imidazolyl, pyrazolyl, pyrrolyl, indazolyl, indolyl, isoindolyl, isoxazolyl, oxazolyl, quinoxalinyl, phthalazinyl, ciiinolinyl, dihydropyrrolyl, pyrrolidinyl, isobenzofuranyl, tetrahydrofuranyl,

dihydropyranyl. The heterocyclyl group may have up to 5, preferably 1,2 or 3 optional substituents. Examples of suitable substituents include halogen, lower alkyl, amino, nitro, cyano, hydroxy, lower alkoxy, carboxy and lower alkyloxy-carbonyls.

The term"halogen"signifies fluorine, chlorine, bromine or iodine and preferably chlorine and fluorine and particularly fluorine.

The term"carboxy", alone or in combination, signifies a-COOH group.

Preferred compounds are compounds of the general formula I wherein n is the integer 1 or 2, m is the integer 0,1 or 2, Rl, R2, R3, R4, R5, R6 and R7 have the meaning given in the formula I above and X represents oxygen.

Examples of preferred compounds are: 1- (9-Oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (l-phenyl-ethyl)-3- (2-n- propyl-phenyl) -urea; 3-Biphenyl-2-yl- (9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-l- (l-phenyl- ethyl) -urea; 3-Naphthalen-1-yl-1-(9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1-phenyl- ethyl)-urea ; 3- (2-Ethyl-phenyl)-1- (9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1-phenyl- ethyl) -urea; 3-(2-Ethoxy-phenyl)-1-(9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1- phenyl-ethyl) -urea; 3- (2-Ethyl-phenyl)-1- (6-fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1-phenyl-ethyl)-urea ; <BR> <BR> <BR> 3-Biphenyl-2-yl-1- (6-fluoro-9-oxo-1, 2, 3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1- phenyl-ethyl) -urea; 1- (6-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1-phenyl-ethyl)-3- (2-n-propyl-phenyl) -urea; 1- (6-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1-phenyl-ethyl)-3- (2-trifluoromethoxy-phenyl)-urea ;

1- (6-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3- (2-isopropyl- phenyl)-1- (1-phenyl-ethyl)-urea ; 1- (6-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3-naphthalen-1-yl-1 (1- phenyl-ethyl) -urea; 1- (7-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (phenyl-ethyl)-3- (2- n-propyl-phenyl) -urea; 1- (7-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (phenyl-ethyl)-3- (2- trifluoromethoxy-phenyl) -urea; 3-Biphenyl-2-yl-1-(7-fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (l- phenyl-ethyl) -urea; 3- (2-Ethyl-phenyl)-1- (7-fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl) -1- (1-phenyl-ethyl)-urea ; 1-(6-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(phenyl-ethyl)-3-(2- n-propyl-phenyl) -urea; 1- (7-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3-(2-ethyl-phenyl)-1- (1-phenyl-ethyl) -urea; 1-(7-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyn olo [2, 1-b] quinazolin-3-yl)-3-naphthalen-1-yl-1 (1- phenyl-ethyl) -urea; 1- (7-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3- (2-isopropyl- phenyl)-1- (1-phenyl-ethyl)-urea ; 1- (7-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(1-phenyl-ethyl)-3- (2-n-propyl-phenyl) -urea; 1- (7-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(phenyl-ethyl)-3-(2- trifluoromethoxy-phenyl) -urea; <BR> <BR> <BR> <BR> 3-Biphenyl-2-yl-1- (7-chloro-9-oxo-1, 2, 3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1- phenyl-ethyl) -urea; 1- (8-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (l-phenyl-ethyl)-3- (2-n-propyl-phenyl)-urea ; 1- (8-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3-(2-ethyl-phenyl)-1- (1-phenyl-ethyl) -urea; 1- (8-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(1-phenyl-ethyl)-3- (2-trifluoromethoxy-phenyl)-urea ;

1- (8-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3-naphthalen-1-yl-1 (1- phenyl-ethyl) -urea; 3-Biphenyl-2-yl-1-(8-chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(1- phenyl-ethyl) -urea; 1-(8-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3-(2-isopropyl- phenyl)-l-(l-phenyl-ethyl)-urea ; 3-Biphenyl-2-yl-1-(6,7-difluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1-phenyl-ethyl)-urea ; 1-(6,7-Difluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(phenyl-ethyl)-3- (2-trifluoromethoxy-phenyl)-urea ; 1-(6,7-Difluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (l-phenyl-ethyl)- 3- (2-n-propyl-phenyl)-urea ; 1- (6, 7-Difluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3-(2-ethyl-phenyl)- 1- (1-phenyl-ethyl)-urea ; 3-BIphenyl-2-yl-1-butyl-1-(9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-urea ; 1-Butyl-1- (9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3- (2-n-propyl-phenyl)- urea; l-Benzyl-3-biphenyl-2-yl-1- (9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-urea ; 1-Benzyl-3- (2-ethoxy-phenyl)-1-(9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)- urea; 1-Benzyl-l- (9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3yl)-3- (2-n-propyl-phenyl)- urea; 3-Biphenyl-2-yl-1-(11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-1- (l- phenyl-ethyl) -urea; 1- l-oXo-6, 8, 9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-1- (l-phenyl-ethyl)-3- (2-n- propyl-phenyl) -urea; 3- (2-Ethyl-phenyl)-1- (11-oxo-6, 8, 9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-1- (1- phenyl-ethyl) -urea; 3-(2-Ethoxy-phenyl)-1-(11-oXo-6, 8,9, 11-tetrahydro-7H-pyrido[2,1-b]quinazolin-6-yl)-1-(1- phenyl-ethyl) -urea; 3-Naphthalen-1-yl-1- l-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-1- (1- phenyl-ethyl) -urea;

3-Biphenyl-2-yl-2-(2,3-difluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6- yl)-1- (1-phenyl-ethyl)-urea ; 1- (2, 3-Difluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido[2,1-b]quinazolin-6-yl)-1-(1-phenyl- ethyl)-3- (2-n-propyl-phenyl)-urea ; 1- (2, 3-Difluoro-1l-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-3- (2-ethyl- phenyl)-1- (1-phenyl-ethyl)-urea ; 1-(2,3-Difluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-3- (2-ethoxy- phenyl)-1- (1-phenyl-ethyl)-urea ; 3-Biphenyl-2-yl-1- (3-fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H pyrido [2, 1-b] quinazolin-6-yl) - 1- (l-phenyl-ethyl)-urea ; 1- (3-Fluoro-11-oxo-6, 8, 9, 11-tekrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-1-(l-phenyl- ethyl)-3- (2-n-propyl-phenyl)-urea ; 3- (2-Ethoxy-phenyl)-1- (3-fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido[1,2-b]quinazolin-6- yl)-l-(1-phenyl-ethyl)-urea ; 3-(2-Ethyl-phenyl)-1-(3-fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido[2,1-b]quinazolin-6- yl)-1- (1-phenyl-ethyl)-urea ; 1- (2-Fluoro-11-oxo-6, 8, 9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-1- (1-phenyl- ethyl)-3- (2-n-propyl-phenyl)-urea ; 3-(2-Ethyl-phenyl)-1-(2-fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6- yl)-1-(1-phenyl-ethyl)-urea ; 1- (2-Fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-1- (l-phenyl- ethyl)-3- (2-trifluoromethoxy-phenyl)-urea ; 3-(2-Ethoxy-phenyl)-1-(2-fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6- yl)-1-(l-phenyl-ethyl)-urea ; 3-Biphenyl-2-yl-1-(2-fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl) - 1- (l-phenyl-ethyl)-urea ; 1- (2-Fluoro-11-oxo-6, 8, 9, 11-tetrahydro-7H-pyrido[2,1-b]quinazolin-6-yl)-3-naphthalen- 1- yl-1-(1-phenyl-ethyl)-urea.

Especially preferred compounds are compounds of the general formula I wherein n is the integer 1 or 2, m is the integer 0, R5 represents methyl, R6 represents phenyl, R1,R2,R3,R4, and R have the meaning given in the formula I above and X represents oxygen.

Examples of especially preferred compounds are: 3-Biphenyl-2-yl- (9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1-phenyl- ethyl) -urea; 3- (2-Ethyl-phenyl)-1- (9-oxo-1, 2, 3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1-phenyl- ethyl) -urea; 3- (2-Ethoxy-phenyl)-1- (9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(1- phenyl-ethyl) -urea; 3-Biphenyl-2-yl-1- (6-fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1- phenyl-ethyl) -urea; 1- (6-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1-phenyl-ethyl)-3- (2-n-propyl-phenyl) -urea; 1- (6-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(1-phenyl-ethyl)-3- (2-trifluoromethoxy-phenyl) -urea; 3-(2-Ethyl-phenyl)-1-(6-fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1-phenyl-ethyl) -urea; 1- (7-Fluoro-9-oxo-1, 2, 3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(phenyl-ethyl)-3-(2- n-propyl-phenyl) -urea; 1- (6-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(phenyl-ethyl)-3-(2- n-propyl-phenyl)-urea ; 1- (7-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3- (2-isopropyl- phenyl)-1- (1-phenyl-ethyl)-urea ; 1- (7-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(1-phenyl-ethyl)-3- (2-n-propyl-phenyl) -urea; 1- (7-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3-(2-ethyl-phenyl)-1- (1-phenyl-ethyl) -urea; 1- (8-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(1-phenyl-ethyl)-3- (2-n-propyl-phenyl) -urea; 1-(8-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3-(2-ethyl-phenyl)-1- (1-phenyl-ethyl)-urea ; 1- (8-Chloro-9-oxo-1, 2, 3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (l-phenyl-ethyl)-3- (2-trifluoromethoxy-phenyl)-urea ;

3-Biphenyl-2-yl-1-(8-chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(1- phenyl-ethyl) -urea; 1- (6, 7-Difluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-l- (l-phenyl-ethyl)- 3- (2-n-propyl-phenyl)-urea ; 1- (6, 7-Difluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3-(2-ethyl-phenyl)- 1- (l-phenyl-ethyl)-urea ; 1- (11-oxo-6,8, 9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-1- (1-phenyl-ethyl)-3- (2-n- propyl-phenyl) -urea; 1-(3-Fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido[2,1-b]quinazolin-6-yl)-1-(1-phenyl- ethyl)-3- (2-n-propyl-phenyl)-urea ; 3-(2-Ethyl-phenyl)-1-(3-fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6- yl)-1- (1-phenyl-ethyl)-urea ; 1-(2, 3-Difluoro-l 1-OXO-6, 8, 9, 11-tetrahydro-7H-pyrido[2,1-b]quinazolin-6-yl)-1-(1-phenyl- ethyl)-3- (2-n-propyl-phenyl)-urea ; 1-(2, 3-Difluoro-l 1-OXO-6, 8,9, 11-tetrahydro-7H-pyrido[2,1-b]quinazolin-6-yl)-3-(2-ethyl- phenyl)-1- (1-phenyl-ethyl)-urea ; 1- (2, 3-Difluoro-1l-oxo-6, 8,9, 11-tetrahydro-7H-pyrido[2,1-b]quinazolin-6-yl)-3-(2-ethoxy- phenyl)-l- (l-phenyl-ethyl)-urea ; 1-(2-Fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido[2,1-b]quinazolin-6-yl)-1-(1-phenyl- ethyl)-3- (2-n-propyl-phenyl)-urea ; 3-(2-Ethyl-phenyl)-1-(2-fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido[2,1-b]quinazolin-6- yl)-1- (1-phenyl-ethyl)-urea ; 3-(2-Ethoxy-phenyl)-1-(2-fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido[2,1-b]quinazolin-6- yl)-1- (1-phenyl-ethyl)-urea ; 1- (5-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-((S)-1-phenyl-ethyl)- 3- (2-n-propyl-phenyl)-urea ; 3-Biphenyl-2-yl-1- (5-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- ((S)-l-phenyl-ethyl)-urea ; 1- (5-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-((S)-1-phenyl-ethyl)- 3- (2-trifluoromethoxy-phenyl)-urea ; 1- (9-Oxo-8-trifluoromethyl-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-((S)-1- phenyl-ethyl)-3- (2-trifluoromethoxy-phenyl)-urea ;

1- (9-Oxo-8-trifluoromethyl-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-((S)-1- phenyl-ethyl) -3- (2-n-propyl-phenyl)-urea ; 3- (2-Ethyl-phenyl)-1- (9-oxo-8-trifluoromethyl-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin- 3-yl)-1-((S)-1-phenyl-ethyl)-urea ; 3-Biphenyl-1-(9-oxo-8-trifluoromethyl-1, 2, 3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- ((S)-1-phenyl-ethyl)-urea.

Examples of physiologically usable or pharmaceutically acceptable salts of the compounds of formula (I) are salts with physiologically compatible mineral acids such as hydrochloric acid, sulphuric or phosphoric acid; or with organic acids such as methanesulphonic acid, acetic acid, trifluoroacetic acid, citric acid, fumaric acid, maleic acid, tartaric acid, succinic acid or salicylic acid. The compounds of formula (I) with free acidic groups can also form salts with physiologically compatible bases.

Examples of such salts are alkali metal, alkali earth metal, ammonium and alkylammoniumsalts such as Na, K, Ca or tetraalkylammonium salt. The compounds of formula (I) can also be present in the form of a zwitterion.

The compounds of formula (I) can contain several asymmetric centres and can be present in the form of optically pure enantiomers, mixtures of enantiomers such as, for example, racemates, optically pure diastereoisomers, mixtures of diastereoisomers, diasteroisomeric racemates or mixtures of diastereoisomeric racemates and the meso- forms.

Preferred compounds as described above have ICso values below 500 nM; especially preferred compounds have IC50 values below 100 nM which have been determinated with the FLIPR (Fluorometric Imaging Plates Reader) method described in the beginning of the experimental section.

The compounds of the general formula (I) and their pharmaceutically usable salts can be used for the treatment of diseases or disorders where an antagonist of a

human orexin receptor is required such as obesity, diabetes, prolactinoma, cardiovascular disorders, cancer, pain, narcolepsy, sleep disorders like insomnia, sleep apnea, parasomnia, depression, anxiety, addictions, schizophrenia, neurodegenerative disorders and dementia.

The compounds of formula (I) and their pharmaceutically usable salts are particularly useful for the treatment of obesity and sleep disorders.

The compounds of formula I may also be used in combination with one or more other therapeutically useful substances e. g. with other orexin receptor antagonists, with lipid lowerer agents, with anorectic agents, with sleep inducing agents, with antidepressants or with other drugs beneficial for the prevention of treatment of obesity or sleep disorders.

The compounds of formula (I) and their pharmaceutically usable salts can be used as medicament (e. g. in the form of pharmaceutical preparations). The pharmaceutical preparations can be administered in enteral or oral form (e. g. in the form of tablets, coated tablets, dragees, hard and soft gelatine capsules, solutions, emulsions or suspensions), nasally (e. g. in the form of nasal sprays) or rectally (e. g. in the form of suppositories). However, the administration can also be effected parentally, such as intramuscularly or intravenously (e. g. in the form of injection solutions).

The compounds of formula (I) and their pharmaceutically usable salts can be processed with pharmaceutically inert, inorganic or organic adjuvants for the production of tablets, coated tablets, dragees, and hard gelatine capsules. Lactose, corn starch or derivatives thereof, talc, stearic acid or its salts etc. can be used, for example, as such adjuvants for tablets, dragees, and hard gelatine capsules.

Suitable adjuvants for soft gelatine capsules, are, for example, vegetable oils, waxes, fats, semi-solid substances and liquid polyols, etc.

Suitable adjuvants for the production of solutions and syrups are, for example, water, polyols, saccharose, invert sugar, glucose, etc.

Suitable adjuvants for injection solutions are, for example, water, alcohols,

polyols, glycerol, vegetable oils, etc.

Suitable adjuvants for suppositories are, for example, natural or hardened oils, waxes, fats, semi-solid or liquid polyols, etc.

Morever, the pharmaceutical preparations can contain preservatives, solubilizers, viscosity-increasing substances, stabilizers, wetting agents, emulsifiers, sweeteners, colorants, flavorants, salts for varying the osmotic pressure, buffers, masking agents or antioxidants. They can also contain still other therapeutically valuable substances.

The invention also relates to processes for the preparation of compounds of Formula I.

The compounds of general formula (I) of the present invention are prepared according to the general sequence of reactions outlined in the schemes below, wherein Rl, R2, R3, R4, R5, R6, R7 are as defined in formula (I) above. As the case may be any compound obtained with one or more optically active carbon atom may be resolved into pure enantiomers or diastereomers, mixtures of enantiomers or diastereomers, diastereomeric racemates and the meso-forms in a manner known per se.

The compounds obtained may also be converted into a pharmaceutically acceptable salt thereof in a manner known per se.

The compounds of general formula (I) may be prepared from the corresponding 2- amino benzoic acid derivatives with the desired lactam by treatment with POC13 (Karimov A. et al Chemistry of Natural Compounds 1982,18, 4,466-472 ; Bhardwaj V. et al Indian Journal of Heterocyclic Chemistry 1999,8, 173-176). Subsequent radical bromination (Kamal A. et al J. Org. Chem. 2001,66, 997-1001) followed by substitution with the corresponding primary amine gave the secondary amine intermediate which is then converted to the desired urea or thiourea compound by reaction with commercially available or synthetized isocyanate or isothiocyanate (Scheme 1) (March J. Advanced Organic Chemistry-Reactions, Mechanisms and Structure 1992, page 418, 4th edition, John Wiley & Sons)

Scheme 1 2-Amino benzoic acid derivatives wherein Rl and R4 are hydrogen and which are not commercially available might be prepared from benzoic acid derivatives using standard procedures (Giencke A. et al Liebigs Ann. Chem. 1990,569-579 ; Follope M. -P. et al Eur. J. med. Chem. 1992,27, 291-295) as described in Scheme 2.

Scheme 2 Furthermore, 2-amino benzoic acid derivatives may also be prepared from aniline derivatives by reaction with chloral hydrate in the presence of hydroxylamine hydrochloride followed by acidic treatment yielding the isatin intermediate. This was converted to the

corresponding anthranilic acid derivative by reaction with hydrogen peroxide under basic conditions (Scheme 3) (Neal Bramson H. et al J. Med. Chefn. 2001,44, 4339-4358; Deady L. W. et al J. Med. Chern. 1997,40, 2040-2046; Rowley M. et al JMed Chem. 1993,36, 3386-3396 ; Hughes P. et al J.Heterocyclic Chem. 1990,27, 2151-2163).

Isatin derivatives Scheme 3 Experimental Section 1. Biology Determination of OXl and OX2 receptor antagonistic activities The OXl and OX2 receptor antagonistic activity of the compounds of formula (I) was determined in accordance with the following experimental method.

Experimental method: Intracellular calcium measurements Chinese hamster ovary (CHO) cells expressing the human orexin-1 receptor or the human orexin-2 receptor, were grown in culture medium (Ham F-12 with L-Glutamine)

containing 300 llg/ml G418, 100 U/ml penicillin, 100 pg/ml streptomycin and 10 % inactivated foetal calf serum (FCS).

The cells were seeded at 80'000 cells/well into 96-well black clear bottom sterile plates (Costar) which had been precoated with 1% gelatine in Hanks'Balanced Salt Solution (HBSS). All reagents were from Gibco BRL.

The seeded plates were incubated overnight at 37°C in 5% CO2.

Human orexin-A as an agonist was prepared as 1 mM stock solution in methanol: water (1: 1), diluted in HBSS containing 0.1 % bovine serum albumin (BSA) and 2 mM HEPES for use in the assay at a final concentration of 10 nM.

Antagonists were prepared as 10 mM stock solution in DMSO, then diluted in 96-well plates, first in DMSO, then in HBSS containing 0.1 % bovine serum albumin (BSA) and 2 mM HEPES.

On the day of the assay, 100 1 of loading medium (HBSS containing 1% FCS, 2 mM HEPES, 5 mM probenecid (Sigma) and 3 uM of the fluorescent calcium indicator fluo-3 AM (1 mM stock solution in DMSO with 10% pluronic acid) (Molecular Probes) was added to each well.

The 96-well plates were incubated for 60 min at 37° C in 5% CO2. The loading solution was then aspirated and cells were washed 3 times with 200 p1 HBSS containing 2.5 mM probenecid, 0. 1 % BSA, 2 mM HEPES. 100 p1 of that same buffer was left in each well.

Within the Fluorescent Imaging Plate Reader (FLIPR, Molecular Devices), antagonists were added to the plate in a volume of 50 ; je, incubated for 20 min and finally 100 1ll of IC5o (nM) °X1 OX2 Example 3 115 79 Example 7 2400 27 Example 28 153 17 Example 30 261 16 Example 33 127 18 Example 40 37 14 Example 41 52 14 Example 44 67 27 Example 49 12 16 Example 50 14 18 Example 51 28 21

Table 1 agonist was added. Fluorescence was measured for each well at 1 second intervals, and the height of each fluorescence peak was compared to the height of the fluorescence peak induced by 10 nM orexin-A with buffer in place of antagonist. For each antagonist, ICso value (the concentration of compound needed to inhibit 50 % of the agonistic response) was determined. The IC50 values of selected compounds are given in Table 1.

II. Chemistrv The following examples illustrate the preparation of pharmacologically active compounds of the invention but do not at all limit the scope thereof. All temperatures are stated in °C.

All hydrochloride salts were prepared by dissolving the free-base in dichloromethane and treating with an excess of ethereal HC1 (2M).

A. Abbreviations AIBN 2,2'-azobisisobutyronitrile BSA Bovine serum albumine CHO Chinese hamster ovary DMF Dimethylformamide eq equivalent ES Electron spray EtOH Ethanol FC Flash chromatography FCS Foetal calf serum FLIPR Fluorescent imaging plate reader HBSS Hank's balanced salt solution HEPES 4- (2-Hydroxyethyl)-piperazine-l-ethanesulfonic acid m multiplet (NMR) MeCN Acetonitrile MeOH Methanol MS Mass spectroscopy NBS N-bromosuccinimide NMR Nuclear magnetic resonance LC Liquid chromatography q quartet (NMR) Rt retention time

rt Room temperature s singlet (NMR) t triplet (NMR) TEA Triethylamine THF Tetrahydrofuran B. 2, 3-Dihydro-1H-pyrrolo [2, 1-b]quinazolin-9-one derivatives General procedure: To a mixture of a 2-aminobenzoic acid derivative (1 g), 2-pyrrolidone (1.5 eq), was added carefully POC13 (2.5 mL). The resulting mixture was stirred at 100°C for 1 h under nitrogen. After cooling, the reaction mixture was poured into ice-water, basified with sat.

NaHCO3, extracted with CH2C12 (3 x 100 mL). The combined extracts were dried (anhydrous MgS04), filtered and concentrated to give a crude brown-yellow viscous oil.

FC (CH2C12/MeOH : 9/1) afforded the title compound as a solid.

1) 2, 3-Dihydro-lH-pyrrolo [2, 1-b] quinazolin-9-one FC (CH2C12/MeOH : 9/1) afforded the title compound as a yellow solid (0.97 g, 71%).

LC-MS (MeCN/H2O : 1/1) : Rt = 2.92 min. m/z = 187 (M + 1).

'H-NMR (30OMHz ; CDC13) # 2.2 (2H, m), 3.2 (2H, m), 4.2 (2H, m), 7.4 (1H, t), 7.7 (1H, m), 8.3 (1H, d).

2) 5-Fluoro-2, 3-dihydro-1H-pyrrolo [2, 1-b] quinazolin-9-one FC (CH2C12/MeOH : 9/1) afforded the title compound as brown solid (0.92 g, 70%).

LC-MS (MeCN/H20 : 1/1) : Rt = 3.21 min. m/z = 205 (M + 1).

1H-NMR (300MHz ; CDC13) # 2.3 (2H, q), 3.25 (2H, t), 4.2 (2H, t), 7. 4 (2H, m), 8. 1 (1H, d).

3) 6-Fluoro-2, 3-dihydro-1H-pyrrolo [2, 1-b] quinazolin-9-one FC (CH2C12/MeOH : 9/1) afforded the title compound as yellow crystals (0.79 g, 60%).

LC-MS (MeCN/H20: 1/1) : Rt = 3.16 min. nilz = 206 (M + 2).

1H-NMR (300MHz ; CDCl3) 6 2. 3 (2H, q), 3.2 (2H, t), 4.2 (2H, t), 7.15 (1H, m), 7.4 (1H, dd), 8.3 (1H, t).

4) 7-Fluoro-2, 3-dihydro-lH-pyrrolo [2, 1-b] quinazolin-9-one FC (CH2C12/MeOH : 9/1) afforded the title compound as yellow crystals (0.97 g, 74%).

LC-MS (MeCN/H20 : 1/1) : Rt = 3.1 min. role = 206 (M + 2).

1H-NMR (300MHz ; CDCl3) a 2.3 (2H, q), 3.2 (2H, t), 4.2 (2H, t), 7.4 (1H, m), 7.7 (1H, m), 7.95 (1H, dd).

5) 6,7-Difluoro-2, 3-dihydro-lH-pyrrolo [2, 1-b] quinazolin-9-one FC (CH2C12/MeOH : 9/1) afforded the title compound as orange crystals (0.86 g, 67%).

LC-MS (MeCN/H20 : 1/1) : Rt = 3.39 min. m/z = 224 (M + 2).

1H-NMR (300MHz ; CDC13) (5 2. 3 (2H, t), 3.2 (2H, t), 4.2 (2H, t), 7.4 (1H, m), 8.00 (1H, m).

6) 6-Chloro-2, 3-dihydro-1H-pyrrolo [2, 1-b]quinazolin-9-one FC (CH2C12/MeOH : 9/1) afforded the title compound as yellow crystals (1. 11 g, 86%).

LC-MS (MeCN/H2O : 1/1) : Rt = 3.55 min. m/z = 222 (M + 2).

1H-NMR (300MHz ; CDC13) S 2.3 (2H, q), 3.2 (2H, t), 4.2 (2H, t), 7.4 (1H, d), 7.6 (1H, s), 8.2 (1H, d).

7) 7-Chloro-2, 3-dihydro-1H-pyrrolo [2, 1-b] quinazolin-9-one FC (CH2C12/MeOH : 9/1) afforded the title compound as a yellow solid (1.14 g, 89%).

LC-MS (MeCN/H20 : 1/1) : Rt = 3.52 min. m/z = 222 (M + 2).

1H-NMR (300MHz ; CDCl3) # 2.3 (2H, q), 3.2 (2H, t), 4.2 (2H, t), 7.6 (2H, q), 8.3 (1H, s).

8) 8-Chloro-2, 3-dihydro-1H-pyrrolo [2, 1-b] quinazolin-9-one FC (CH2C12/MeOH : 9/1) afforded the title compound as a yellow solid (0.97g, 75%).

LC-MS (MeCN/H2O : 1/1) : Rt = 3.30 min. m/z=222 (M + 2).

1H-NMR (300MHz ; CDC13) 8 2. 3 (2H, q), 3.2 (2H, t), 4.2 (2H, t), 7.4 (1H, m), 7.6 (2H, m).

9) 8-Trifluoromethyl-2, 3-dihydro-1H-pyrrolo [2, 1-b] quinazolin-9-one A mixture of 2-amino-6-trifluoromethyl-benzoic acid (0.97 g), 2-methoxypyrroline (0.703 g, 1.5 eq) in dry toluene (12 mL) was stirred at reflux for 3h. The orange solution was then evaporated to dryness to give a crude orange solid FC (CH2Cl2/MeOH : 9/1) afforded the title compound as a yellow powder (0. 89g, 74%).

LC-MS (MeCN/H2O : 1/1) : Rt = 3.90 min. m/z = 255 (M + 1).

'H-NMR (300MHz ; CDCl3) 2.3 (2H, q), 3.2 (2H, t), 4.25 (2H, t), 7.75 (1H, t), 7.85 (2H, d).

C. 3-Bromo-2, 3-dihydro-IH-pyrrolo [2, 1-b] quinazolin-9-one derivatives General procedure: A mixture of a 2,3-Dihydro-1H-pyrrolo [2, 1-b] quinazolin-9-one derivative (1 eq), NBS (1 eq), AIBN (0.085 eq) in dry CHC13 (20 mL/g) was stirred at reflux for 20 h under nitrogen. After cooling, the mixture was concentrated under reduced pressure, the resulting crude solid was purified by FC (AcOEt/heptane: 7/3) to give the title compound.

1) 3-Bromo-2, 3-dihydro-IH-pyrrolo [2, 1-b] quinazolin-9-one FC (AcOEt/heptane: 7/3) afforded the title compound as brown crystals (40%).

LC-MS (MeCN/H2O : 1/1) : Rt = 3.49 min. nilz = 266 (M + 1).

1H-NMR (300MHz ; CDC13) 8 2.55-2. 8 (2H, m), 4.1-4. 5 (2H, m), 5.3 (1H, d), 7.5 (1H, m), 7.7 (1H, m), 8.3 (1H, d).

2) 3-Bromo-5-fluoro-2, 3-dihydro-lH-pyrrolo [2, 1-b] quinazolin-9-one FC (AcOEt/heptane: 7/3) afforded the title compound as a n orange solid (35%).

LC-MS (MeCN/H20 : 1/1) : Rt = 3.77 min. m/z = 285 (M +2).

1H-NMR (300MHz ; CDC13) 5 2.6-2. 85 (2H, m), 4.2-4. 45 (2H, m), 5.35 (1H, d), 7.5 (2H, m), 8.1 (1H, d).

3) 3-Bromo-6-fluoro-2, 3-dihydro-IH-pyrrolo [2, 1-b] quinazolin-9-one FC (AcOEt/heptane: 7/3) afforded the title compound as a n orange solid (52%).

LC-MS (MeCN/H20 : 1/1) : Rt = 3.70 min. m/z = 284 (M + 1).

1H-NMR (300MHz ; CDCl3) # 2.55-2. 8 (2H, m), 4.1-4. 5 (2H, m), 5.3 (1H, d), 7.2 (1H, m), 7.5 (1H, m), 8.3 (1H, m).

4) 3-Bromo-7-fluoro-2, 3-dihydro-IH-pyrrolo [2, 1-b] quinazolin-9-one FC (AcOEt/heptane: 7/3) afforded the title compound as a reddish solid (53%).

LC-MS (MeCN/H2O : 1/1) : Rt = 3.65 min. m/z = 284 (M + 1).

1H-NMR (300MHz ; CDCl3) J 2.6-2. 85 (2H, m), 4.2-4. 5 (2H, m), 5.3 (1H, d), 7.5 (1H, m), 7.7 (1H, m), 7.95 (1H, m).

5) 3-Bromo-6, 7-difluoro-2, 3-dihydro-1H-pyrrolo [2, 1-b] quinazolin-9-one FC (AcOEt/heptane: 7/3) afforded the title compound as a red solid (69%).

LC-MS (MeCN/H2O : 1/1) : Rt = 4.01 min. m/z = 302 (M + 1).

1H-NMR (300MHz ; CDC13) # 2.55-2. 8 (2H, m), 4.05-4. 5 (2H, m), 5.3 (1H, d), 7.5 (1H, m), 8.1 (lH, m).

6) 3-Bromo-6-chloro-2, 3-dihydro-IH-pyrrolo [2, 1-b] quinazolin-9-one FC (AcOEt/heptane: 7/3) afforded the title compound as a reddish solid (42%).

LC-MS (MeCN/H20 : 1/1') : Rt = 4.16 min. m/z = 300 (M + 1).

1H-NMR (300MHz ; CDC13) # 2.6-2. 85 (2H, m), 4.1-4. 5 (2H, m), 5.3 (1H, d), 7.5 (1H, dd), 7.7 (1H, s), 8.3 (1H, d).

7) 3-Bromo-7-chloro-2, 3-dihydro-lH-pyrrolo [2, 1-b] quinazolin-9-one FC (AcOEt/heptane: 7/3) afforded the title compound as a pink solid (49%).

LC-MS (MeCN/HaO : 1/1) : Rt = 4.12 min. m/z = 300 (M + 1).

1H-NMR (300MHz ; CDCl3) # 2.55-2. 85 (2H, m), 4.1-4. 5 (2H, m), 5.3 (1H, d), 7.7 (2H, s), 8.3 (1H, s).

8) 3-Bromo-8-ehloro-2S3-dihydro-lH-pyrrolo [21-b] quinazolin-9-one FC (AcOEt/heptane: 7/3) afforded the title compound as a violet powder (38%).

LC-MS (MeCN/H20: 1/1) : Rt = 3.56 min. m/z = 300 (M + 1).

1H-NMR (300MHz ; CDC13) # 2.55-2. 85 (2H, m), 4.1-4. 5 (2H, m), 5.3 (1H, d), 7.5 (1H, dd), 7.8 (2H, m).

9) 3-Bromo-8-trifluoromethyl-2,3-dihydro-1H-pyrrolo [2, 1-b] quinazolin-9-one FC (AcOEt/heptane: 7/3) afforded the title compound as a red solid (36%).

LC-MS (MeCN/H2O : 1/1) : Rt = 4. 47 min. m/z = 334 (M + 1).

'H-NMR (300MHz ; CDC13) # 2.55-2. 85 (2H, m), 4.2-4. 5 (2H, m), 5.3 (1H, d), 7.8 (1H, t), 7.9 (2H, m).

C. 3- (1-Phenyl-ethylamino)-2, 3-dihydro-IH-pyrrolo [2, 1-b] quinazolin-9-one derivatives General procedure A mixture of a 3-bromo-2, 3-dihydro-IH-pyrrolo [2, 1-b] quinazolin-9-one derivative (0.56 g, 2.11 mmol), (D, L)-a-methylbenzylamine (1 eq), TEA (1.5 eq) in dry EtOH (10 mL), was stirred at reflux for 20h under nitrogen. After cooling, the reaction mixture was combined with CH2C12/water and the aqueous phase was extracted twice with CH2CI2.

The combined extracts were dried (anhydrous MgS04), filtered and concentrated to give a dark green residue as mixture of diastereoisomers.

1) 3- (1-Phenyl-ethylamino)-2, 3-dihydro-IH-pyrrolo [2, 1-b] quinazolin-9-one FC (AcOEt/heptane: 7/3) afforded the title compound as a dark green solid (69%).

LC-MS (MeCN/H2O : 1/1) : Rt = 3.00 min. m/z = 306 (M + 1).

2) 6-Fluoro-3- (1-phenyl-ethylamino)-2, 3-dihydro-IH-pyrrolo [2, 1-b] quinazolin-9- one FC (AcOEt/heptane: 7/3) afforded the title compound as a dark oil (56%).

LC-MS (MeCN/H20 : 1/1) : Rt = 3.18 min. m/z = 324 (M + 1).

3) 7-Fluoro-3- (1-phenyl-ethylamino)-2, 3-dihydro-lH-pyrrolo [2, 1-b] quin azolin-9- one FC (AcOEt/heptane: 7/3) afforded the title compound as a dark brown oil (62%).

LC-MS (MeCN/H2O : 1/1) : Rt = 3.06 min. m/z = 324 (M + 1).

4) 6, 7-Difluoro-3- (1-phenyl-ethylamino)-2, 3-dihydro-IH-pyrrolo [2, 1- b] quinazolin-9-one FC (AcOEt/heptane: 7/3) afforded the title compound as a dark green oil (42%).

LC-MS (MeCN/H2O : 1/1) : Rt = 3.31 min. nilz = 342 (M + 1).

5) 6-Chloro-3-(1-phenyl-ethylamino)-2,3-dihydro-1H-pyrrolo [2, 1-b]quinazolin- 9-one FC (AcOEt/heptane: 7/3) afforded the title compound as a dark green oil (50%).

LC-MS (MeCN/H20 : 1/1) : Rt = 3.40 min. m/z = 340 (M + 1).

6) 7-Chloro-3- (1-phenyl-ethylamino)-2, 3-dihydro-IH-pyrrolo [2, 1-b] quinazolin- 9-one FC (AcOEt/heptane : 7/3) afforded the title compound as a dark brown oil (54%).

LC-MS (MeCN/H2O : 1/1) : Rt = 3.34 min. iizlz = 340 (M + 1).

7) 8-Chloro-3- (1-phenyl-ethylamino)-2, 3-dihydro-lH-pyrrolo [2, 1-b] quinazolin- 9-one FC (AcOEt/heptane: 7/3) afforded the title compound as a dark brown oil (71%).

LC-MS (MeCN/H2O : 1/1) : Rt = 3.21 min. m/z = 340 (M + 1).

8) 3-((S)-1-Phenyl-ethylamino)-8-trifluoromethyl-2,3-dihydro-1H -pyrrolo [2, 1- b] quinazolin-9-one Reaction with the (S)-a-methylbenzylamine FC (AcOEt) afforded the title compound as a dark brown oil (68%).

LC-MS (MeCN/H20 : 1/1) : Rt = 3.63 min. m/z = 374 (M + 1).

9) 5-Fluoro-3-((S)-l-phenyl-ethylamino)-2, 3-dihydro-lH-pyrrolo [2, 1-b] quinazolin-9- one Reaction with the (S)-a-methylbenzylamine FC (AcOEt) afforded the title compound as a dark green oil (58%).

LC-MS (MeCN/H2O : 1/1) : Rt = 3.36 min. m/z = 324 (M + 1).

D. 6,7, 8,9-Tetrahydro-pyrido [2, 1-b] quinazolin-11-one derivatives General procedure To a suspension of 2-aminobenzoic acid derivative (1 eq) in dry CHC13 (20 mL/g), was added slowly POC13 (1.3 eq) accompanied by stirring for 15 min at rt under nitrogen.

Then 8-valerolactam (1.1 eq) was added portionwise over a period of 10 min, the reaction mixture was stirred at reflux under nitrogen for 3 h. Aqueous HCl 5% was added to the reaction mixture, the aqueous phase was separated (this operation was repeated three times). The combined aqueous extracts were clarified by adding active charcoal and filtered through celite. The resulting pale yellow solution was basified with concentrated aqueous ammoniac and extracted with CH2C12 (three times). The combined organic extracts were washed with water, dried (anhydrous Na2S04), concentrated under reduced pressure to give a solid which was used for the next step without further purification.

1) 6,7, 8,9-Tetrahydro-pyrido [2, 1-b] quinazolin-11-one Light orange crystals (41%) LC-MS (MeCN/H2O : 1/1) : Rt = 2.83 min. m/z = 201 (M + 1).

1H-NMR (300MHz ; CDCl3) a 2.00 (4H, m), 3.1 (2H, t), 4.1 (2H, t), 7.5 (1H, t), 7.6-7. 8 (2H, m), 8.3 (1H, d).

2) 3-fluoro-6, 7,8, 9-tetrahydro-pyrido [2, 1-b] quinazolin-11-one Yellow crystals (44%) LC-MS (MeCN/H2O : 1/1) : Rt = 3.34 min. m/z = 219 (M + 1).

1H-NMR (300MHz ; CDC13) 8 2.00 (4H, m), 3.0 (2H, t), 4.1 (2H, t), 7.1 (1H, m), 7.2 (1H, d), 8.3 (1H, t).

3) 2-fluoro-6, 7,8, 9-tetrahydro-pyrido [2, 1-b] quinazolin-11-one Yellow solid (56%) LC-MS (MeCN/H20 : 1/1) : Rt = 3.39 min. 771/Z = 219 (M + 1).

1H-NMR (300MHz ; CDC13) # 2.00 (4H, m), 3.0 (2H, t), 4.1 (2H, t), 7.4 (1H, m), 7.6 (1H, m), 7.9 (1H, dd).

4) 2,3-Difluoro-6,7,8,9-tetrahydro-pyrido[2,1-b]quinazolin-11-o ne

Yellow crystals (45%) LC-MS (MeCN/H2O : 1/1) : Rt =3.82 min. m/z = 237 (M + 1).

1H-NMR (300MHz ; CDC13) a 2.00 (4H, m), 2.95 (2H, t), 4.1 (2H, t), 7.35 (1H, q), 8.0 (1H, t).

E. 6-Bromo-6, 7,8, 9-tetrahydro-pyrido [2, 1-b] quinazolin-11-one derivatives These compounds have been prepared as described for the 3-bromo-2, 3-dihydro-lH- pyrrolo [2, 1-b] quinazolin-9-one derivatives.

1) 6-Bromo-6, 7,8, 9-tetrahydro-pyrido [2, 1-b] quinazolin-11-one Pale yellow crystals (55%).

LC-MS (MeCN/H2O : 1/1) : Rt = 3.86 min. m/z = 280 (M + 1).

IH-NMR (300MHz ; CDCl3) a 2.1-2. 6 (4H, m), 4.00 (1H, m), 4.4 (1H, m), 5.4 (1H, s), 7.5 (lH, t), 7.7 (2H, m), 8.3 (1H, d).

2) 6-Bromo-3-fluoro-6,7, 8,9-Tetrahydro-pyrido [2, 1-b] quinazolin-11-one Pale yellow crystals (65%).

LC-MS (MeCN/H2O : 1/1) : Rt = 4.21 min. m/z = 298 (M + 1).

1H-NMR (300MHz ; CDC13) # 2.1-2. 6 (4H, m), 4.00 (1H, m), 4.4 (1H, m), 5.4 (1H, s), 7.2-7. 5 (2H, m), 8.3 (1H, d).

3) 6-Bromo-2-fluoro-6, 7,8, 9-tetrahydro-pyrido [2, 1-b] quinazolin-11-one White solid (69%).

LC-MS (MeCN/H20 : 1/1) : Rt = 4.20 min. m/z = 298 (M + 1).

1H-NMR (300MHz ; CDC13) a 2.1-2. 6 (4H, m), 4.00 (1H, m), 4.4 (1H, m), 5.35 (1H, s), 7.5 (1H, m), 7.7 (1H, m), 7.9 (1H, dd).

4) 6-Bromo-2, 3-difluoro-6, 7,8, 9-tetrahydro-pyrido [2, 1-b] quinazolin-11-one White solid (55%).

LC-MS (MeCN/H20 : 1/1) : Rt = 4.49 min. 17lez = 316 (M + 1).

1H-NMR (300MHz ; CDCl3) # 2.1-2. 6 (4H, m), 3.95 (1H, m), 4.4 (1H, m), 5.35 (1H, s), 7.45 (1H, t), 8.05 (1H, t).

F. 6- (1-Phenyl-ethylamino)-6, 7,8, 9-tetrahydro-pyrido [2, 1-b] quinazolin-11-one derivatives These compounds have been prepared as decribed for the 3-(1-phenyl-ethylamino)-2, 3- dihydro-lH-pyrrolo [2, 1-b] quinazolin-9-one derivatives (mixture of diastereoisomers).

1) 6-(1-Phenyl-ethylamino)-6, 7,8, 9-tetrahydro-pyrido [2, 1-b] quinazolin-11-one Pale yellow solid (72%).

LC-MS (MeCN/H2O : 1/1) : Rt = 2.98 and 3.19 min. m/z = 320 (M + 1).

2) 3-Fluoro-6- (l-phenyl-ethylamino)-6, 7,8, 9-tetrahydro-pyrido [2, 1-b] quinazolin- 11-one Yellow solid (40%).

LC-MS (MeCN/ H2O : 1/1) : Rt = 3.18 min. m/z = 338 (M + 1).

3) 2-Fluoro-6-(1-phenyl-ethylamino)-6, 7,8, 9-tetrahydro-pyrido [2, 1-b] quinazolin- 11-one Yellow solid (26%).

LC-MS (MeCN/H20 : 1/1) : Rt = 3.14 min. iiilz = 338 (M + 1).

4) 2, 3-Difluoro-6- (1-phenyl-ethylamino)-6, 7,8, 9-tetrahydro-pyrido [2, 1- b] quinazolin-11-one Yellow solid (40%).

LC-MS (MeCN/H20 : 1/1) : Rt = 3.15 min. m/z = 356 (M + 1).

Example 1 1- (9-Oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1-phenyl-ethyl)-3- (2-n- propyl-phenyl)-urea (mixture of diatereoisomers) To a solution of 3-(1-phenyl-ethylamino)-2,3-dihydro-1H-pyrrolo [2, 1-b] quinazolin-9-one (50 mg, 0.163 mmol) in dry CH2Cl2 (1 mL), was added 2-n-propylphenyl isocyanate (26.3 mg, 0.163 mmol). The resulting reaction mixture was stirred at rt under nitrogen for 20h.

The reaction mixture was then concentrated under reduced pressure and the residue was

purified by FC (AcOEt/heptane: 7/3) to give the title compound as a white foam (45%).

LC-MS (MeCN/H20 : 1/1) : Rt = 3.00 min. m/z = 467 (M + 1).

Example 2 3-Biphenyl-2-yl-1- (9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(1- phenyl-ethyl) -urea (mixture of diatereoisomers) In analogy to Example 1 using with 2-biphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a white foam (63%).

LC-MS (MeCN/H20 : 1/1) : Rt = 4.89 and 5.49 min. m/z = 500 (M).

Example 3 3- (2-Ethoxy-phenyl)-1- (9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1- phenyl-ethyl) -urea (mixture of diatereoisomers) In analogy to Example 1 using 2-ethoxyphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a white foam (55%).

LC-MS (MeCN/H2O : 1/1) : Rt = 4.60 and 5.23 min. m/z = 468 (M).

Example 4 3-(2-Ethyl-phenyl)-1-(6-fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3- yl)-1- (1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 6-fluoro-3-(1-phenyl-ethylamino)-2,3-dihydro-1H- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-ethylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a white foam (62%).

LC-MS (MeCN/H2O : 1/1) : Rt = 4.76 and 5.33 min. m/z = 470 (M).

Example 5 3-Biphenyl-2-yl-1- (6-fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)- 1- (1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 6-fluoro-3- (l-phenyl-ethylamino)-2, 3-dihydro-lH- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-biphenylisocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a white foam (82%).

LC-MS (MeCN/H20 : 1/1) : Rt = 5.01 and 5.61 min. dz = 518 (M).

Example 6 1- (6-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1-phenyl- ethyl)-3- (2-n-propyl-phenyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 6-fluoro-3-(1-phenyl-ethylamino)-2,3-dihydro-1H- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-n-propylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige powder (61%).

LC-MS (MeCN/H2O : 1/1) : Rt = 5.06 and 5.61 min. m/z = 484 (M).

Example 7 1- (6-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1-phenyl- ethyl)-3- (2-trifluoromethoxy-phenyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 6-fluoro-3-(1-phenyl-ethylamino)-2,3-dihydro-1H- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-trifluoromethoxyphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a white solid (72%).

LC-MS (MeCN/H2O : 1/1) : Rt = 4.92 and 5.61 min. m/z = 526 (M).

Example 8 1- (6-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3-(2-isopropyl- phenyl)-1- (1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 6-fluoro-3-(1-phenyl-ethylamino)-2,3-dihydro-1H- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-isopropylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a white foam (70%).

LC-MS (MeCN/H20 : 1/1) : Rt = 4.98 and 5. 48 min. filz = 484 (M).

Example 9 1- (6-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3-naphthalen-1- yl-1 (1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 6-fluoro-3- (1-phenyl-ethylamino)-2, 3-dihydro-IH pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 1-naphthyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a brown oil (77%).

LC-MS (MeCN/H20 : 1/1) : Rt = 4.72 and 5.28 min. mlz = 492 (M).

Example 10 1- (7-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b]quinazolin-3-yl)-1-(phenyl-ethyl)- 3- (2-propyl-phenyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 7-fluoro-3-(1-phenyl-ethylamino)-2,3-dihydro-1H- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-n-propylphenyl isocyanate (1 eq).

FC (AcOEt/heptane : 7/3) afforded the title compound as an orange oil (75%).

LC-MS (MeCN/ H2O : 1/1) : Rt = 4.99 and 5.53 min. m/z = 484 (M).

Example 11 1- (7-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b]quinazolin-3-yl)-1-(phenyl-ethyl)- 3- (2-trifluoromethoxy-phenyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 7-fluoro-3-(1-phenyl-ethylamino)-2,3-dihydro-1H- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-trifluoromethoxyphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a brown oil (83%).

LC-MS (MeCN/H20 : 1/1) : Rt = 4.85 and 5.52 min. m/z = 526 (M +1).

Example 12 3-Biphenyl-2-yl-1- (7-fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)- 1- (1-phenyl-ethyl)-urea (mixture of diatereoisomers)

In analogy to Example 1 using 7-fluoro-3- (1-phenyl-ethylamino)-2, 3-dihydro-IH- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-biphenylisocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a yellow brown oil (70%).

LC-MS (MeCN/H2O : 1/1) : Rt = 5.02 and 5.59 min. nilz = 518 (M).

Example 13 3- (2-Ethyl-phenyl)-l- (7-fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3- yl)-1- (1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 7-fluoro-3- (1-phenyl-ethylamino)-2, 3-dihydro-IH pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-ethylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige foam (70%).

LC-MS (MeCN/H2O : 1/1) : Rt = 4.77 and 5.32 min. m/z = 470 (M).

Example 14 3-Biphenyl-2-yl-1-(6,7-difluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3- yl)-1- (1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 6, 7-difluoro-3-(1-phenyl-ethylamino)-2,3-dihydro-1H- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-biphenylisocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a pale grey foam (56%).

LC-MS (MeCN/H20 : 1/1) : Rt = 5.27 and 5.84 min. m/z = 536 (M).

Example 15 1- (6, 7-Difluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(phenyl- ethyl)-3- (2-trifluoromethoxy-phenyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 6, 7-difluoro-3- (1-phenyl-ethylamino)-2, 3-dihydro-lH- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-trifluromethoxyphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a brown foam (61 %).

LC-MS (MeCN/H2O : 1/1) : Rt = 5.07 and 5.74 min. fnlz = 544 (M).

Example 16 1- (6, 7-Difluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1-phenyl- ethyl)-3- (2-n-propyl-phenyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 6, 7-difluoro-3-(1-phenyl-ethylamino)-2,3-dihydro-1H- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-n-propylphenyl isocyanate (1 eq).

FC (AcOEt/heptane : 7/3) afforded the title compound as a brown foam (67%).

LC-MS (MeCN/H20 : 1/1) : Rt = 5.22 and 5.74 min. 714/Z = 502 (M).

Example 17 1- (7-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3-(2-ethyl- phenyl)-1- (1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 7-chloro-3-(1-phenyl-ethylamino)-2,3-dihydro-1H- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-ethylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a pale beige foam (66%).

LC-MS (MeCN/H2O : 1/1) : Rt = 5.09 and 5.73 min. m/z = 487 (M).

Example 18 1- (7-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b]quinazolin-3-yl)-3-naphthalen-1- yl-1 (1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 7-chloro-3- (1-phenyl-ethylamino)-2, 3-dihydro-IH pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 1-naphthyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige solid (47%).

LC-MS (MeCN/H20 : 1/1) : Rt = 4.99 and 5.61 min. milz = 509 (M).

Example 19 1- (7-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b]quinazolin-3-yl)-3-(2-isopropyl- phenyl)-1- (1-phenyl-ethyl)-urea (mixture of diatereoisomers)

In analogy to Example 1 using 7-chloro-3-(1-phenyl-ethylamino)-2,3-dihydro-1H- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-isopropylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a grey solid (87%).

LC-MS (MeCN/H20 : 1/1) : Rt = 5.30 and 5. 81 min. m/z=501 (M).

Example 20 1- (7-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1-phenyl- ethyl)-3- (2-n-propyl-phenyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 7-chloro-3-(1-phenyl-ethylamino)-2, 3-dihydro-lH- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-n-propylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a white foam (58%).

LC-MS (MeCN/H20 : 1/1) : Rt = 5.34 and 5.92 min. m/z = 501 (M).

Example 21 1- (7-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(phenyl-ethyl)- 3- (2-trifluoromethoxy-phenyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 7-chloro-3-(1-phenyl-ethylamino)-2, 3-dihydro-lH- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-trifluoromethoxyphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a pale brown foam (74%).

LC-MS (MeCN/H20 : 1/1) : Rt = 5.18 and 5.92 min. m/z = 542 (M).

Example 22 3-Biphenyl-2-yl-l- (7-chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)- 1- (1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 7-chloro-3-(1-phenyl-ethylamino)-2,3-dihydro-1H- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-biphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a white foam (72%).

LC-MS (MeCN/H2O : 1/1) : Rt = 5.36 and 5.99 min. m/z = 535 (M).

Example 23 3-Biphenyl-2-yl-1- (11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-1-(1- phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 6- (1-phenyl-ethylamino)-6, 7,8, 9-tetrahydro-pyrido [2, 1- b] quinazolin-11-one (1 eq) and 2-biphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a yellow oil (22%).

LC-MS (MeCN/H2O : 1/1) : Rt = 4.99 and 5.80 min. m/z = 515 (M + 1).

Example 24 1- (11-Oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-1- (1-phenyl-ethyl)-3- (2-n-propyl-phenyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 6-(1-phenyl-ethylamino)-6, 7,8, 9-tetrahydro-pyrido [2, 1- b] quinazolin-11-one (1 eq) and 2-n-propylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige foam (53%).

LC-MS (MeCN/ H2O : 1/1) : Rt= 5.18 and 5.86 min. nilz = 481 (M + 1).

Example 25 3- (2-Ethyl-phenyl)-1- (11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-1- (1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 6- (l-phenyl-ethylamino)-6, 7,8, 9-tetrahydro-pyrido [2, 1- b] quinazolin-11-one (1 eq) and 2-ethylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a yellow oil (72%).

LC-MS (MeCN/H2O : 1/1) : Rt = 4.87 and 5.54 min. m/z = 467 (M + 1).

Example 26 3-(2-Ethoxy-phenyl)-1-(11-oxo-6,8, 9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)- 1- (l-phenyl-ethyl)-urea (mixture of diatereoisomers)

In analogy to Example 1 using 6-(1-phenyl-ethyalmino)-6, 7, 8, 9-tetrahydro-pyrido [2, 1- b] quinazolin-ll-one (1 eq) and 2-ethoxyphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige solid (41%).

LC-MS (MeCN/H20 : 1/1) : Rt = 4.81 and 5.67 min. inlz = 483 (M + 1).

Example 27 3-Naphthalen-1-yl-1-(11-oxo-6, 8, 9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-1- (1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 6-(1-phenyl-ethylamino)-6, 7,8, 9-tetrahydro-pyrido [2, 1- b] quinazolin-11-one (1 eq) and 1-naphthyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige solid (28%).

LC-MS (MeCN/H2O : 1/1) : Rt = 4.87 and 5.51 min. m/z = 489 (M + 1).

Example 28 1- (2, 3-Difluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-1-(1- phenyl-ethyl)-3- (2-n-propyl-phenyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 2, 3-difluoro-6-(1-phenyl-ethylamino)-6, 7,8, 9-tetrahydro- pyrido [2, 1-b]quinazolin-11-one (1 eq) and 2-n-propylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige foam (80%).

LC-MS (MeCN/H20 : 1/1) : Rt = 6.13 min. m/z = 517 (M + 1).

Example 29 3-Biphenyl-2-yl-1-(2, 3-difluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1- b] quinazolin-6-yl)-1- (1-phenylethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 2, 3-difluoro-6- (l-phenyl-ethylamino)-6, 7,8, 9-tetrahydro- pyrido [2, 1-b] quinazolin-11-one (1 eq) and 2-biphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige foam (48%).

LC-MS (MeCN/ H2O : 1/1) : Rt = 5.57and 6.22 min. m/z = 551 (M + 1).

Example 30 1- (2, 3-Difluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyridol2, 1-b] quinazolin-6-yl)-3-(2- ethyl-phenyl)-1- (1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 2, 3-difluoro-6- (1-phenyl-ethylamino)-6, 7,8, 9-tetrahydro- pyrido [2, 1-b] quinazolin-11-one (1 eq) and 2-ethylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige foam (97%).

LC-MS (MeCN/H2O : 1/1) : Rt= 5.35 and 5.92 min./ = 503 (M + 1).

Example 31 1- (2, 3-Difluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b]quinazolin-6-yl)-3-(2- ethoxy-phenyl)-1-(1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 2, 3-difluoro-6-(1-phenyl-ethylamino)-6, 7,8, 9-tetrahydro- pyrido [2, 1-b] quinazolin-11-one (1 eq) and 2-ethoxyphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige foam (60%).

LC-MS (MeCN/H20 : 1/1) : Rt = 5.22 and 6.07 min. m/z = 519 (M + 1).

Example 32 3-Biphenyl-2-yl-1- (3-fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin- 6-yl)-1- (1-phenylethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 3-fluoro-6-(1-phenyl-ethylamino)-6, 7,8, 9-tetrahydro- pyrido [2, 1-b] quinazolin-11-one (1 eq) and 2-biphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige foam (42%).

LC-MS (MeCN/H2O : 1/1) : Rt = 5. 38 and 6.10 min. into = 533 (M + 1).

Example 33 1- (3-Fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-1- (l- phenyl-ethyl)-3- (2-n-propyl-phenyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 3-fluoro-6-(1-phenyl-ethylamino)-6, 7,8, 9-tetrahydro- pyrido [2, 1-b] quinazolin-1l-one (1 eq) and 2-n-propylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige foam (98%).

LC-MS (MeCN/H20 : 1/1) : Rt = 5.29 and 5.96 min. filz = 499 (M + 1).

Example 34 3-(2-Ethoxy-phenyl)-1-(3-fluoro-11-oxo-6,8, 9, 11-tetrahydro-7H-pyrido [2, 1- b] quinazolin-6-yl)-1- (l-phenylethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 3-fluoro-6-(1-phenyl-ethylamino)-6, 7,8, 9-tetrahydro- pyrido [2, 1-b] quinazolin-11-one (1 eq) and 2-ethoxyphenyl isocyanate (1 eq).

FC (AcOEt/heptane : 7/3) afforded the title compound as a foam (88%).

LC-MS (: MeCN/H2O : 1/1) : Rt = 5.03 and 5.93 min. nilz = 501 (M + 1).

Example 35 3-(2-Ethyl-phenyl)-1-(3-fluoro-11-oxo-6,8, 9, 11-tetrahydro-7H-pyrido [2, 1- b] quinazolin-6-yl)-1- (l-phenylethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 3-fluoro-6-(1-phenyl-ethylamino)-6, 7,8, 9-tetrahydro- pyrido [2, 1-b] quinazolin-11-one (1 eq) and 2-ethylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a foam (47%).

LC-MS (MeCN/H2O : 1/1) : Rt = 5.07 and 5.74 min. m/z = 485 (M + 1).

Example 36 3-Biphenyl-2-yl-1-(2-fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin- 6-yl)-1- (1-phenylethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 2-fluoro-6-(1-phenyl-ethylamino)-6, 7,8, 9-tetrahydro- pyrido [2, 1-b] quinazolin-11-one (1 eq) and 2-biphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a yellow powder (43%).

LC-MS (MeCN/ H2O : 1/1) : Rt = 5.38 and 6.07 min. nilz = 533 (M + 1).

Example 37 1-(2-Fluoro-11-oxo-6, 8, 9, 11-tetrahydro-7H-pyrido [2, 1-b] quinazolin-6-yl)-I- (I- phenyl-ethyl)-3- (2-n-propyl-phenyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 2-fluoro-6-(1-phenyl-ethylamino)-6, 7, 8, 9-tetrahydro- pyrido [2, 1-b] quinazolin-11-one (1 eq) and 2-n-propylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as an orange-brown powder (53%).

LC-MS (MeCN/H2O : 1/1) : Rt = 5.29 and 5.94 min. m/z = 499 (M + 1).

Example 38 3-(2-Ethoxy-phenyl)-1-(2-fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2, 1- b] quinazolin-6-yl)-1- (1-phenylethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 2-fluoro-6- (1-phenyl-ethylamino)-6, 7,8, 9-tetrahydro- pyrido [2, 1-b] quinazolin-11-one (1 eq) and 2-ethoxyphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a yellow powder (44%).

LC-MS (MeCN/ H2O : 1/1) : Rt = 5.03 and 5.86 min. m/z = 501 (M + 1).

Example 39 3-(2-Ethyl-phenyl)-1-(2-fluoro-11-oxo-6, 8,9, 11-tetrahydro-7H-pyrido [2,1- b] quinazolin-6-yl)-1- (1-phenylethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 2-fluoro-6- (l-phenyl-ethylamino)-6, 7,8, 9-tetrahydro- pyrido [2, 1-b] quinazolin-11-one (1 eq) and 2-ethylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a yellow powder (54%).

LC-MS (MeCN/ H2O : 1/1) : Rt = 5.07 and 5.72 min. m/z = 485 (M + 1).

Example 40 1- (8-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-(phenyl-ethyl)- 3- (2-trifluoromethoxy-phenyl)-urea (mixture of diatereoisomers)

In analogy to Example 1 using 8-chloro-3-(1-phenyl-ethylamino)-2,3-dihydro-1H- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-trifluoromethoxyphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a white foam (74%).

LC-MS (MeCN/H2O : 1/1) : Rt = 4.97 and 5.74 min. m/z = 542 (M).

Example 41 3-Biphenyl-2-yl-l- (8-chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-bJquinazolin-3-yl)- 1-(1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 8-chloro-3- (1-phenyl-ethylamino)-2, 3-dihydro-IH pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-biphenylisocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a yellow foam (70%).

LC-MS (MeCN/H2O : 1/1) : Rt = 5.16 and 5. 80 min. mlz = 535 (M).

Example 42 1- (8-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3-(2-isopropyl- phenyl)-1- (1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 8-chloro-3-(1-phenyl-ethylamino)-2,3-dihydro-1H- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-isopropylphenyl isocyanate (1 eq).

FC (AcOEt/heptane : 7/3) afforded the title compound as a beige foam (70%).

LC-MS (MeCN/H20 : 1/1) : Rt = 5.11 and 5.67 min. m/z = 501 (M).

Example 43 1- (8-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-3-naphthalen-1- yl-1 (1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 8-chloro-3-(1-phenyl-ethylamino)-2, 3-dihydro-lH- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 1-naphthyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige foam (57%).

LC-MS (MeCN/H2O : 1/1) : Rt = 4.83 and 5.46 min. falz = 509 (M).

Example 44 1- (8-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1- (1-phenyl- ethyl)-3- (2-n-propyl-phenyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 8-chloro-3- (1-phenyl-ethylamino)-2, 3-dihydro-IH pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-n-propylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige foam (64%).

LC-MS (MeCN/ H2O : 1/1) : Rt = 5.11 and 5.74 min. nilz = 501 (M).

Example 45 1- (8-Chloro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b]quinazolin-3-yl)-3-(2-ethyl- phenyl)-1- (1-phenyl-ethyl)-urea (mixture of diatereoisomers) In analogy to Example 1 using 8-chloro-3-(1-phenyl-ethylamino)-2,3-dihydro-1H- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-ethylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a pale beige foam (83%).

LC-MS (MeCN/H2O : 1/1) : Rt =4.86 and 5.53 min. tnlz = 486 (M).

Example 46 1- (5-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-((S)-1-phenyl- ethyl)-3- (2-n-propyl-phenyl)-urea In analogy to Example 1 using 5-fluoro-3-((S) l-phenyl-ethylamino)-2, 3-dihydro-lH- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-n-propylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a pale beige foam (57%).

LC-MS (MeCN/H2O : 1/1) : Rt =5.27 and 5.74 min. inlz = 485 (M + 1).

Example 47 3-Biphenyl-2-yl-l- (5-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)- 1-((S)-1-phenyl-ethyl)-urea In analogy to Example 1 using 5-fluoro-3-((S) l-phenyl-ethylamino)-2, 3-dihydro-lH- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-biphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a green foam (73%).

LC-MS (MeCN/HaO : 1/1) : Rt =5.39 and 5.94 min. m/z = 519 (M + 1).

Example 48 1- (5-Fluoro-9-oxo-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-((S)-1-phenyl- ethyl)-3- (2-trifluoromethoxy-phenyl)-urea In analogy to Example 1 using 5-fouoro-3-((S)1-phenyl-ethylamino)-2,3-dihydro-1H- pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-trifluoromethoxyphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a pale green solid (62%).

LC-MS (MeCN/H2O : 1/1) : Rt =5.13 and 5.72 min. m/z = 527 (M + 1).

Example 49 1- (9-Oxo-8-trifluoromethyl-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-((S)- 1-phenyl-ethyl)-3-(2-trifluoromethoxy-phenyl)-urea In analogy to Example 1 using 3-((S)-l-Phenyl-ethylamino)-8-trifluoromethyl-2, 3- dihydro-1H-pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-trifluoromethoxyphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige foam (68%).

LC-MS (MeCN/H2O : 1/1) : Rt =5.39 and 6.14 min. m/z = 577 (M + 1).

Example 50 1- (9-Oxo-8-trifluoromethyl-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3-yl)-1-((S)- 1-phenyl-ethyl)-3-(2-n-propyl-phenyl)-urea In analogy to Example 1 using 3-((S)-l-Phenyl-ethylamino)-8-trifluoromethyl-2, 3- dihydro-lH-pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-n-propylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige foam (54%).

LC-MS (MeCN/ H2O : 1/1) : Rt =5. 54 and 6.13 min. m/z = 535 (M + 1).

Example 51 3- (2-Ethyl-phenyl)-1- (9-oxo-8-trifluoromethyl-1, 2,3, 9-tetrahydro-pyrrolo [2, 1- b] quinazolin-3-yl)-1-((S)-l-phenyl-ethyl)-urea In analogy to Example 1 using 3-((S)-l-Phenyl-ethylamino)-8-trifluoromethyl-2, 3- dihydro-lH-pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-ethylphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige foam (62%).

LC-MS (MeCN/H2O : 1/1) : Rt =5.34 and 5.96 min. nilz = 521 (M + 1).

Example 52 3-Biphenyl-1- (9-oxo-8-trifluoromethyl-1, 2,3, 9-tetrahydro-pyrrolo [2, 1-b] quinazolin-3- yl)-1-((S)-1-phenyl-ethyl)-urea In analogy to Example 1 using 3-((S)-l-Phenyl-ethylamino)-8-trifluoromethyl-2, 3- dihydro-1H-pyrrolo [2, 1-b] quinazolin-9-one (1 eq) and 2-biphenyl isocyanate (1 eq).

FC (AcOEt/heptane: 7/3) afforded the title compound as a beige foam (72%).

LC-MS (MeCN/ H2O : 1/1) : Rt =5.64 and 6.22 min. m/z = 569 (M + 1).