The invention is concerned with novel pyrrole derivatives, a process for their manufacture, pharmaceutical compositions and the use of such compounds in medicine, especially in the treatment of viral diseases. In particular, the compounds are inhibitors of the human immunodeficiency virus reverse transcriptase enzyme which is involved in viral replication. Consequently the compounds of this invention may be advantageously used as therapeutic agents for the treatment of diseases mediated by the human immunodeficiency virus (HIV).

The disease Acquired Immunodeficiency Syndrome (AIDS) is the end result of infection by the distinct retroviruses, human immunodeficiency virus type-1 (HIV-1) or type-2 (HIV-2). Several critical points in the virus's life cycle have been identified as possible targets for therapeutic intervention. Inhibition of one of these, the transcription of viral RNA to viral DNA (reverse transcriptase, RT), has provided a number of the current therapies used in treating AIDS. Inhibition of reverse transcriptase provided the first form of treatment for HIV infection with 3'-azido-3'-deoxythymidine (AZT). Since then several inhibitors have been launched, broadly forming two classes : nucleoside analogues and non-nucleosides. As an example of the latter it has been found that certain benzoxazinones, e. g. efavirenz are useful in the inhibition of HIV RT. However, development of strains of the virus resistant to current RT inhibitors is a constant problem. Therefore, development of compounds effective against resistant strains is an important goal.

Meanwhile, explorations into pyrrole derivatives have been undertaken with the view of utilising them as medicines.

US Patent 3,644,631 describes pyrrole derivatives effective for the therapy of inflammatory syndromes.

US Patent 4,282,242 describes pyrrole derivatives effective for the therapy of lowering the blood glucose level in hyperglycemic mammals.

The object of the present invention is to provide novel compounds which are potent inhibitors of the human immunodeficiency virus reverse transcriptase enzyme, which is involved in viral replication, and which accordingly show a potential to be efficacious as antiviral drugs.

This object could be achieved with the compounds of formula I wherein Rl is alkyl, cycloalkyl, aryl or heterocyclyl ; R2 is alkyl, cycloalkyl, aryl or heterocyclyl ; R3 is hydrogen, alkyl, cycloalkyl, aryl or heterocyclyl ; R4 is hydrogen, alkyl, carboxyl, C (=O) R, CONR'R", cyano or alkenyl, wherein R is hydrogen, alkyl, alkoxy, trifluoromethyl, methyl-oxy-carbonyl or ethyl-oxy- carbonyl, and wherein R'and R", are independently of each other, hydrogen, alkyl or aryl; RS is alkyl, aryl or a group-Z-C (=O) R"', wherein Z is a single bond or-CH=CH-, and wherein R"'is hydrogen or alkyl ; X represents S, S (O), S (0) 2, O, N (alkyl) or X-R2 together represent CH2-aryl or CH2-heterocyclyl ; and with the proviso that only one of R3 and R4 is hydrogen and alkyl in R3 is not CF3 ; and hydrolyzable esters or ethers thereof or a pharmaceutically acceptable salt thereof.

The term"alkyl"as used herein, and if not specified by the number of carbon atoms, denotes an optionally substituted straight or branched chain hydrocarbon residue containing 1 to 7 carbon atoms, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, sec- butyl, isobutyl, tert.-butyl, pentyl, hexyl, heptyl, including their different isomers.

Suitable substituents for the alkyl chain can be selected from one or more of aryl, heterocyclyl, carboxyl, alkoxy, cycloalkyl oxy, aryl oxy, heterocyclyl oxy, hydroxy, amino carbonyl oxy, alkyl amino carbonyl oxy, dialkyl amino carbonyl oxy, aryl amino carbonyl oxy, heterocyclyl amino carbonyl oxy, alkyl carbonyl, cycloalkyl carbonyl, aryl carbonyl, heterocyclyl carbonyl, hydroxy carbonyl, alkoxy carbonyl, cycloalkyl oxy carbonyl, aryl oxy carbonyl, heterocyclyl oxy carbonyl, amino carbonyl, alkyl amino carbonyl, dialkyl amino carbonyl, cycloalkyl amino carbonyl, aryl amino carbonyl, heterocyclyl amino carbonyl, amino, alkyl amino, dialkyl amino, cycloalkyl amino, aryl amino, heterocyclyl amino, alkyl carbonyl amino, cycloalkyl carbonyl amino, aryl carbonyl amino, heterocyclyl carbonyl amino, alkoxy carbonyl amino, cycloalkyl oxy carbonyl amino, aryloxy carbonyl amino, heterocylyl oxy carbonyl amino, alkyl amino carbonyl amino, dialkyl amino carbonyl amino, cycloalkyl amino carbonyl amino, aryl amino carbonyl amino, heterocyclyl amino carbonyl amino, alkyl sulfonyl amino, cycloalkyl sulfonyl amino, aryl sulfonyl amino, heterocyclyl sulfonyl amino, nitro, alkyl sulfinyl, cycloalkyl sulfinyl, aryl sulfinyl, heterocyclyl sulfinyl, alkyl sulfonyl, cycloalkyl sulfonyl, aryl sulfonyl, heterocyclyl sulfonyl, alkyl thio, cycloalkyl thio, aryl thio, heterocyclyl thio or

halogen.

In case more than one substituent is attached to the alkyl group, these substituents can be identical or different from each other.

The suitable substituents for the alkyl group aryl and heterocyclyl may be substituted with 1-3 substituents, preferably 1-2 substituents, more preferably 1 substituent selected from Cl 4-alkyl (preferably methyl), Cl-4-alkoxy (preferably methoxy), halogen (preferably chlorine) or trifluoromethyl. Examples for substituted alkyl are cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, 2-pyridylmethyl, 2-pyridylethyl, 2-pyridylpropyl, 2-pyridylbutyl, methyl-2-pyridyl-methyl, methyl-2-pyridyl-ethyl, dimethyl-2-pyridyl-methyl, ethyl-2-pyridyl-methyl, methoxy-2-pyridyl-methyl, methoxy- 2-pyridyl-ethyl, dimethoxy-2-pyridyl-methyl, fluoro-2-pyridyl-methyl, difluoro-2-pyridyl- methyl, chloro-2-pyridyl-methyl, chloro-2-pyridyl-ethyl, dichloro-2-pyridyl-methyl, dichloro-2-pyridyl-methyl, bromo-2-pyridyl-methyl, dibromo-2-pyridyl-methyl, 3-pyridyl-methyl, 3-pyridyl-ethyl, 3-pyridyl-propyl, 3-pyridyl-butyl, methyl-3-pyridyl- methyl, methyl-3-pyridyl-ethyl, dimethyl-3-pyridyl-methyl, ethyl-3-pyridyl-methyl, methoxy-3-pyridyl-methyl, methoxy-3-pyridyl-ethyl, dimethoxy-3-pyridyl-methyl, fluoro- 3-pyridyl-methyl, difluoro-3-pyridyl-methyl, chloro-3-pyridyl-methyl, chloro-3-pyridyl- ethyl, dichloro-3-pyridyl-methyl, dichloro-3-pyridyl-methyl, bromo-3-pyridyl-methyl, dibromo-3-pyridyl-methyl, 4-pyridyl-methyl, 4-pyridyl-ethyl, 4-pyridyl-propyl, 4-pyridyl- butyl, methyl-4-pyridyl-methyl, methyl-4-pyridyl-ethyl, dimethyl-4-pyridyl-methyl, ethyl- 4-pyridyl-methyl, 2- (trifluoromethyl)-4-pyridyl-1-methyl, 3- (trifluoromethyl)-4-pyridyl- 1-methyl, 2- (trifluoromethyl)-3-pyridyl-1-methyl, 4- (trifluoromethyl)-3-pyridyl-1- methyl, 3- (trifluoromethyl)-2-pyridyl-l-methyl, 4- (trifluoromethyl)-2-pyridyl-l-methyl, methoxy-4-pyridyl-methyl, methoxy-4-pyridyl-ethyl, dimethoxy-4-pyridyl-methyl, fluoro- 4-pyridyl-methyl, difluoro-4-pyridyl-methyl, chloro-4-pyridyl-methyl, chloro-4-pyridyl- ethyl, dichloro-4-pyridyl-methyl, dichloro-4-pyridyl-methyl, bromo-4-pyridyl-methyl, dibromo-4-pyridyl-methyl, phenylmethyl (benzyl), phenylethyl, phenylpropyl, phenylbutyl, 2-methylphenylmethyl, 3-methylphenylmethyl, 4-methylphenylmethyl, 2-methylphenylethyl, 3-methylphenylethyl, 4-methylphenylethyl, 2,3- dimethylphenylmethyl, 2,4-dimethylphenylmethyl, 2,5-dimethylphenylmethyl, 2,6-dimethylphenylmethyl, 3,4-dimethylphenylmethyl, 3,5-dimethylphenylmethyl, 3,6-dimethylphenylmethyl, 2-ethylphenylmethyl, 3-ethylphenylmethyl, 4-ethylphenylmethyl, 2,3-diethylphenylmethyl, 2,4-diethylphenylmethyl, 2,5-diethylphenylmethyl, 2,6-diethylphenylmethyl, 3,4-diethylphenylmethyl, 3,5-diethylphenylmethyl, 3,6-diethylphenylmethyl, 2-trifluoromethyl-phenylmethyl, 3-trifluoromethyl-phenylmethyl, 4-trifluoromethyl-phenylmethyl, 2-trifluoromethyl- phenylethyl, 3-trifluoromethyl-phenylethyl, 4-trifluoromethyl-phenylethyl, 2,3-di-

trifluoromethyl-phenylmethyl, 2,4-di-trifluoromethyl-phenylmethyl, 2,5-di- trifluoromethyl-phenylmethyl, 2,6-di-trifluoromethyl-phenylmethyl, 3,4-di- trifluoromethyl-phenylmethyl, 3,5-di-trifluoromethyl-phenylmethyl, 3,6-di- trifluoromethyl-phenylmethyl, 2-methoxy-phenylmethyl, 3-methoxy-phenylmethyl, 4-methoxy-phenylmethyl, 2-methoxy-phenylethyl, 3-methoxy-phenylethyl, 4-methoxy- phenylethyl, dimethoxy-phenylmethyl, dimethoxy-phenylethyl, 2,4,6-trimethoxy- phenylmethyl, 2-ethoxy-phenylmethyl, 3-ethoxy-phenylmethyl, 4-ethoxy-phenylmethyl, ethoxy-phenylethyl, diethoxy-phenylmethyl, diethoxy-phenylethyl, 2, 4,6-triethoxy- phenylmethyl, 2-fluorophenylmethyl, 3-fluorophenylmethyl, 4-fluorophenylmethyl, 2,3-difluorophenylmethyl, 2,4-difluorophenylmethyl, 2,5-difluorophenylmethyl, 2,6-difluorophenylmethyl, 3,4-difluorophenylmethyl, 3,5-difluorophenylmethyl, 3,6-difluorophenylmethyl, 2-fluorophenylethyl, 3-fluorophenylethyl or 4-fluorophenylethyl, 2-chlorophenylmethyl, 3-chlorophenylmethyl, 4-chlorophenylmethyl, 2,3-dichlorophenylmethyl, 2,4-dichlorophenylmethyl, 2,5-dichlorophenylmethyl, 2,6-dichlorophenylmethyl, 3,4-dichlorophenylmethyl, 3,5-dichlorophenylmethyl, 3,6-dichlorophenylmethyl, 2-chlorophenylethyl, 3-chlorophenylethyl, 4-chlorophenylethyl, 2-bromophenylmethyl, 3-bromophenylmethyl, 4-bromophenylmethyl, 2,3-dibromophenylmethyl, 2,4-dibromophenylmethyl, 2,5-dibromophenylmethyl, 2,6-dibromophenylmethyl, 3,4-dibromophenylmethyl, 3,5-dibromophenylmethyl, 3,6-dibromophenylmethyl, 2-bromophenylethyl, 3-bromophenylethyl or 4-bromophenylethyl. 2-phenyl-phenylmethyl, 3-phenyl- phenylmethyl, 4-phenyl-phenylmethyl, 2-phenoxy-phenylmethyl, 3-phenoxy- phenylmethyl, 4-phenoxy-phenylmethyl, 2-nitro-phenylmethyl, 3-nitro-phenylmethyl, 4-nitro-phenylmethyl, 2-amino-phenylmethyl, 3-amino-phenylmethyl, 4-amino- phenylmethyl, 2-dimethylamino-phenylmethyl, 3-dimethylamino-phenylmethyl, 4-dimethylamino-phenylmethyl, 2-cyano-phenylmethyl, 3-cyano-phenylmethyl, 4-cyano- phenylmethyl, 2-methanesulfonyl-phenylmethyl, 3-methanesulfonyl-phenylmethyl, 4-methanesulfonyl-phenylmethyl, 2-acid methyl ester-phenylmethyl, 3-acid methyl ester- phenylmethyl, 4-acid methyl ester-phenylmethyl, 2-thiazolyl-methyl, 4-thiazolyl-methyl, 5-thiazolyl-methyl, benzothiophenyl-2-methyl, 4-chloro-benzothiophenyl-2-methyl, 5-chloro-benzothiophenyl-2-methyl, 6-chloro-benzothiophenyl-2-methyl, 7-chloro- benzothiophenyl-2-methyl, benzothiophenyl-3-methyl, 4-chloro-benzothiophenyl- 3-methyl, 5-chloro-benzothiophenyl-3-methyl, 6-chloro-benzothiophenyl-3-methyl, 7-chloro-benzothiophenyl-3-methyl, quinolinyl-2-methyl, quinolinyl-3-methyl, quinolinyl-6-methyl, 4-chloro-quinolinyl-6-methyl, 2- (trifluoromethyl)-quinolinyl- 6-methyl, 4-chloro-2- (trifluoromethyl)-quinolinyl-6-methyl, 2-pyrimidyl, 4-pyrimidyl or 2 [1, 3,5-triazinyl].

Alkyl in R'is preferably an unsubstituted straight or branched chain hydrocarbon residue containing 1 to 7 carbon atoms as defined above or substituted Cl 7-alkyl with 1-3 substituents, preferably 1-2 substituents, more preferably 1 substituent selected from heterocyclyl, aryl and cycloalkyl. Alkyl in Rl is more preferable methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert.-butyl, 2-pyridylmethyl, 2-pyridylethyl, 2-pyridylpropyl, 2-pyridylbutyl, 3-pyridylmethyl, 3-pyridylethyl, 3-pyridylpropyl, 3-pyridylbutyl, 4-pyridylmethyl, 4-pyridylethyl, 4-pyridylpropyl, 4-pyridylbutyl, phenylmethyl (benzyl), cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, 2-methoxy-phenylmethyl, 3-methoxy-phenylmethyl, 4-methoxy- phenylmethyl, 2,3-dimethoxy-phenylmethyl, 2,4-dimethoxy-phenylmethyl, 2,5-dimethoxy-phenylmethyl, 2,6-dimethoxy-phenylmethyl, 3,4-dimethoxy-phenylmethyl, 3,5-dimethoxy-phenylmethyl, 2,4,6-trimethoxy-phenylmethyl, 2-thiazolyl-methyl, 4-thiazolyl-methyl, 5-thiazolyl-methyl, benzothiophenyl-2-methyl, 4-chloro- benzothiophenyl-2-methyl, 5-chloro-benzothiophenyl-2-methyl, 6-chloro- benzothiophenyl-2-methyl, 7-chloro-benzothiophenyl-2-methyl, benzothiophenyl- 3-methyl, 4-chloro-benzothiophenyl-3-methyl, 5-chloro-benzothiophenyl-3-methyl, 6-chloro-benzothiophenyl-3-methyl, 7-chloro-benzothiophenyl-3-methyl, quinolinyl- 2-methyl, quinolinyl-3-methyl, quinolinyl-6-methyl, 4-chloro-quinolinyl-6-methyl, 2-(trifluoromethyl)-quinolinyl-6-methyl or 4-chloro-2-(trifluoromethyl)-quinolinyl- 6-methyl, 2-(trifluoromethyl)-4-pyridyl-1-methyl, 3-(trifluoromethyl)-4-pyridyl- 1-methyl, 2- (trifluoromethyl)-3-pyridyl-1-methyl, 4- (trifluoromethyl)-3-pyridyl- <BR> <BR> <BR> 1-methyl, 3-(trifluoromethyl)-2-pyridyl-1-methyl, 4-(trifluoromethyl)-2-pyridyl-1-methyl or N-benzylamidomethyl. Further preferred alkyl substituents for Rl are methyl, ethyl, isopropyl, cyclohexylmethyl, phenylmethyl or pyridylmethyl. Most preferred alkyl substituents for Rl is 4-pyridylmethyl.

Alkyl in R2 is preferably an unsubstituted straight or branched chain hydrocarbon residue containing 1 to 7 carbon atoms as defined above, more preferable methyl, ethyl, n- propyl, isopropyl, n-butyl, sec-butyl, isobutyl or tert.-butyl. Further preferred alkyl substituents for R are methyl or n-propyl. Most preferred alkyl in R2 is methyl.

Alkyl in R3 is preferably an unsubstituted straight or branched chain hydrocarbon residue containing 1 to 7 carbon atoms as defined above or substituted Cl 7-alkyl with 1-3 substituents, preferably 1-2 substituents, more preferably 1 substituent selected from heterocyclyl. More preferable alkyl in R3 is methyl, ethyl, n-propyl, isopropyl, n-butyl, sec- butyl, isobutyl, tert.-butyl, 2-pyridylmethyl, 2-pyridylethyl, 3-pyridylmethyl, 3- pyridylethyl, 4-pyridylmethyl, 4-pyridylethyl. Further preferred alkyl substituents for R3 are isopropyl, n-propyl or pyridylmethyl. Most preferred alkyl in R3 is isopropyl. Alkyl in R3 is not CF3.

Alkyl in R4 is preferably an unsubstituted straight or branched chain hydrocarbon residue containing 1 to 7 carbon atoms as defined above or substituted Cl 7-alkyl (preferably Cl 2-alkyl) with 1-3 substituents, preferably 1-2 substituents, more preferably 1 substituent selected from hydroxy, amino, Cl 4-alkoxy (preferably, Cl 2-aLkoxy), phenyl, methyl-oxy-carbonyl, ethyl-oxy-carbonyl, azido, 2-pyridyl-carbonyl-amino, 3-pyridyl- carbonyl-amino, 4-pyridyl-carbonyl-amino, (phenoxy)-carbonyl-amino, (methoxy)- carbonyl-amino, (di-methyl-amino)-carbonyl-amino, (phenyl-amino)-carbonyl-amino, (amino)-carbonyl-amino, (phenyl)-carbonyl-amino, (methyl)-carbonyl-amino, methyl- carbonyl-amino-methyl-carbonyl-amino, (tert.-butyl)-carbonyl-amino-methyl-carbonyl- amino, methyl-sulfonyl-amino, phenyl-sulfonyl-amino, p-toluyl-sulfonyl-amino, (N1- acetyl-O-tert.-butyl-N2-yl)-L-serinamide, (Nl-acetyl-N2-yl)-L-serinamide and [Nl-. (tert.- butoxycarbonyl)-O-tert.-butyl-N2-yl]-L-serinamide. More preferred substituents for Cl 7-alkyl (preferably Cl-2-alkyl) are selected from hydroxy, amino, Cl 2-alkoxy, 2-pyridyl- carbonyl-amino, 3-pyridyl-carbonyl-amino, 4-pyridyl-carbonyl-amino, (phenoxy)- carbonyl-amino, (methoxy)-carbonyl-amino, (di-methyl-amino)-carbonyl-amino, (phenyl-amino)-carbonyl-amino, (amino)-carbonyl-amino, (phenyl)-carbonyl-amino, (methyl)-carbonyl-amino, methyl-carbonyl-amino-methyl-carbonyl-amino, (tert.-butyl)- carbonyl-amino-methyl-carbonyl-amino, (Nl-acetyl-0-tert.-butyl-N2-yl)-L-serinamide, (Nl-acetyl-N2-yl)-L-serinamide and [Nl-(tert.-butoxycarbonyl)-O-tert.-butyl-N2-yl]-L- serinamide. Most preferred substituents for Cl 7-alkyl (preferably Cl 2-aLkyl) are selected from hydroxy, 2-pyridyl-carbonyl-amino, 3-pyridyl-carbonyl-amino, 4-pyridyl-carbonyl- amino, (phenoxy)-carbonyl-amino, (methoxy)-carbonyl-amino, (di-methyl-amino)- carbonyl-amino, (phenyl-amino)-carbonyl-amino, (amino)-carbonyl-amino, (phenyl)- carbonyl-amino, (methyl)-carbonyl-amino, methyl-carbonyl-amino-methyl-carbonyl- amino, (tert.-butyl)-carbonyl-amino-methyl-carbonyl-amino, (Nl-acetyl-O-tert.-butyl- N2-yl)-L-serinamide, (Nl-acetyl-N2-yl)-L-serinamide and [Nl-(tert.-butoxycarbonyl)-O- tert.-butyl-N2-yl]-L-serinamide. In case more than one substituent is attached to the alkyl group, these substituents can be identical or different from each other. Alkyl in R4 is more preferable methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert.-butyl, hydroxy-methyl, l-hydroxy-ethyl, 2-hydroxy-ethyl, 1,2-ethanediol, 1,2-propanediol, amino-methyl, amino-ethyl, methoxy-methyl, methoxy-ethyl, phenyl-methanol, (methyl- oxy-carbonyl)- (hydroxy-methyl), (ethyl-oxy-carbonyl)- (hydroxy-methyl), azido-methyl, azido-ethyl, 2-pyridyl-carbonyl-amino-methyl, 3-pyridyl-carbonyl-amino-methyl, 4- pyridyl-carbonyl-amino-methyl, (amino-methyl)-carbonyl-amino-methyl, (phenoxy)- carbonyl-amino-methyl, (methoxy)-carbonyl-amino-methyl, (di-methyl-amino)- carbonyl-amino-methyl, (phenyl-amino)-carbonyl-amino-methyl, (amino)-carbonyl- amino-methyl, (phenyl)-carbonyl-amino-methyl, (methyl)-carbonyl-amino-methyl, methyl-carbonyl-amino-methyl-carbonyl-amino-methyl, (tert.-butyl)-carbonyl-amino- methyl-carbonyl-amino-methyl, (Nl-acetyl-O-tert.-butyl-N2-ylmethyl)-L-serinamide,

(Nl-acetyl-N2-yl] methyl)-L-serinamide, [Nl- (tert.-butoxycarbonyl)-O-tert.-butyl-N2-yl- methyl]-L-serinamide, methyl-sulfonyl-amino-methyl, phenyl-sulfonyl-amino-methyl or p-toluyl-sulfonyl-amino-methyl. Preferred alkyl for R4 is unsubstituted Cl 7-alkyl (preferably Cl-4-akl) or substituted Cl 7-alkyl (preferably Cl-4-alkyl, more preferred Ci-2- alkyl) with hydroxy or amino or methoxy as substituents. More preferable alkyl in R4 is methyl or ethyl substituted with a hydroxy group or a methoxy group or (methyl)- carbonyl-amino-methyl. Further preferred alkyl groups for R4 are methyl or ethyl substituted with a hydroxy group or a methoxy. More preferred alkyl in R4 is methyl substituted with a hydroxy group or (methyl)-carbonyl-amino-methyl. Most preferred alkyl in R4 is methyl substituted with a hydroxy group.

Alkyl in R is preferably an unsubstituted straight or branched chain hydrocarbon residue containing 1 to 7 carbon atoms (preferably, Cl 4-alkyl), as defined above or substituted Cl 7-alkyl (preferably Cl-4-alkyl, more preferred Cl 2-alkyl) with 1-3 substituents, preferably 1-2 substituents, more preferably 1 substituent selected from hydroxy, Ci. 4-alkoxy (preferably methoxy or ethoxy), methyl-carbonyl-oxy or amino- carbonyl-oxy. Alkyl in R5 is more preferable methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert.-butyl, hydroxy-methyl, 1-hydroxy-ethyl, 2-hydroxy-ethyl, 1,2-ethanediol, 1,2-propanediol, methoxy-methyl, ethoxy-methyl, (methyl-carbonyl-oxy)- methyl, (amino-carbonyl-oxy)-methyl. More preferable alkyl in R5 is methyl, ethyl, n- propyl, isopropyl or substituted Cl 2-alkyl substituted with 1-3 substituents selected from hydroxy, methyl-carbonyl-oxy and amino-carbonyl-oxy. Further preferred alkyl in R5 is methyl, ethyl, (amino-carbonyl-oxy)-methyl or Cl 2-alkyl substituted with a hydroxy group. Another preferred alkyl in Rus vis methyl or (amino-carbonyl-oxy)-methyl, most preferred alkyl in R5 is methyl.

In another preferred embodiment of the invention, alkyl in R5 is unsubstituted alkyl or substituted alkyl with hydroxy as substituent, more preferably wherein alkyl in R5 is methyl or ethyl optionally substituted with a hydroxy group, and most preferred wherein alkyl in R5 is methyl.

Alkyl in R, R', R"and R"'is preferably an unsubstituted straight or branched chain hydrocarbon residue containing 1 to 7 carbon atoms as defined above and more preferably methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert.-butyl.

Alkyl for N (alkyl) is preferably an unsubstituted straight or branched chain hydrocarbon residue containing 1 to 7 carbon atoms and most preferred methyl.

The term"cycloalkyl"as used herein, and if not specified by the number of carbon atoms, denotes an optionally substituted cycloalkyl group containing 3 to 8 carbon atoms,

e. g. cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl or cyclooctyl. The term "cycloalkyl"preferably denotes a cycloalkyl group containing 3 to 6 carbon atoms.

Suitable substituents for cycloalkyl can be selected from those named for alkyl, in addition however an oxo group (=O) can be added to the selection.

Cycloalkyl in R'and R'are as defined above.

Cycloalkyl in R3 denotes an optionally substituted cycloalkyl group containing 3 to 8 carbon atoms, preferably 3 to 6 carbon atoms. Most preferred cycloalkyl in R3 denotes a cyclopropyl group.

The term"alkoxy"as used herein, and if not specified by the number of carbon atoms, denotes a straight or branched chain alkyl-oxy group wherein the"alkyl"portion is as defined above such as methoxy, ethoxy, n-propyloxy, isopropyloxy, n-butyloxy, isobutyloxy, tert.-butyloxy, pentyloxy, hexyloxy, heptyloxy including their different isomers. More preferred alkoxy groups within the invention are methoxy, ethoxy, n- propyloxy, isopropyloxy, n-butyloxy, isobutyloxy or tert.-butyloxy.

Alkoxy in R is as defined above.

The term"alkenyl"as used herein, and if not specified by the number of carbon atoms, denotes an unsubstituted or substituted hydrocarbon chain radical having from 2 to 8 carbon atoms, preferably from 2 to 4 carbon atoms, and having at least one olefinic double bond, including their different isomers. Examples are vinyl or allyl.

Alkenyl in R4 is as defined above.

The term"C (=O) R," as used herein for R4, denotes a hydrogen atom, an Cl 7-alkyl group (preferably Cl-4-alkyl as defined above for the alkyl substituent R), alkoxy (preferably Cl-4-alkoxy), trifluoromethyl, methyl-oxy-carbonyl, ethyl-oxy-carbonyl, each of these substituents attached to a keto function-C (=O)-. Preferred examples are an aldehyde group (C (=O) H), methyl-carbonyl, ethyl-carbonyl, tert.-butoxy-carbonyl, trifluoromethyl-carbonyl, methyl-oxy-dicarbonyl or ethyl-oxy-carbonyl.

The term"CONR'R""as used herein for R4, denotes, independently of each other, hydrogen, Cl 7-alkyl (preferably Ci. 4-alkyl), substituted aryl (preferably phenyl), each of these substituents attached to a amino-carbonyl function. Preferred examples are amino- carbonyl (CONH2), (methyl-amino)-carbonyl, (dimethyl-amino)-carbonyl, (phenyl- amino)-carbonylv or (2,4,6-trimethoxy-methyl)-amino-carbonyl.

The term"-Z-C (=O) R"'"as used herein for R5, wherein Z is a single bond or -CH=CH-and R"'is hydrogen or alkyl (preferably Cl 4-alkyl) denotes an aldehyde group (C (=O) H), methyl-carbonyl or ethyl-carbonyl, aldehyde-ethylene (-CH=CH) C (=O) H), (methyl-carbonyl)-ethylene (-CH=CH) C (=O) CH3) or (ethyl-carbonyl)-ethylene (-CH=CH) C (=O) C2Hs). The ethylene group of the invention can have the (E) or (Z) configuration. Both isomeric forms of these compounds are embraced by the present invention.

The term"aryl"as used herein denotes an optionally substituted phenyl and naphthyl, both optionally benz-fused to an optionally substituted saturated, partially unsaturated or aromatic monocyclic, bicyclic or tricyclic heterocycle or carbocycle e. g. to cyclohexyl or cyclopentyl.

Suitable substituents for aryl can be selected from those named for alkyl, in addition however Cl 4-alkyl, trifluoromethyl, trifluoromethoxy, C2 4-alkenyl, 1,2-propanediol, cyano and hydroxy-methyl can be added to the selection.

In case more than one substituent is attached to the aryl group, these substituents can be identical or different from each other.

Aryl in Rl is preferably an unsubstituted or substituted phenyl with suitable substituents selected from 1 to 5 of halogen, nitro and unsubstituted straight or branched chain alkyl containing 1 to 4 carbon atoms.

Aryl in R2 is preferably an unsubstituted or substituted phenyl or naphthyl (preferably phenyl) with suitable substituents selected from 1 to 5 substituents, preferably 1-4 substituents, more preferably 1-3 substituent selected from Cl 7-alkyl (preferable Cl-4-alkyl), trifluoromethyl, Cl-4-alkoxy (preferable Cl_2-alkoxy), trifluoromethoxy, C2-4- alkenyl, 1,2-propanediol, fluorine, chlorine, bromine, iodine, nitro, cyano, phenyl, hydroxy-methyl, 4-pyridyl, 3-pyridyl and 2-pyridyl (preferably 1-3 substituent selected from Cl 7-aLkyl (preferable Ci. 4-alkyl), halogen and nitro; more preferably 1-3 substituent selected from halogen; most preferably 1-3 substituent selected from chlorine). In case more than one substituent is attached to the aryl group, these substituents can be identical or different from each other. Examples of substituted aryl groups are 2-methyl-phenyl, 3-methyl-phenyl, 4-methyl-phenyl, 2-ethyl-phenyl, 3-ethyl-phenyl, 4-ethyl-phenyl, 2,3-dimethylphenyl, 2,4-dimethylphenyl, 2,5-dimethylphenyl, 2,6-dimethylphenyl, 3,4-dimethylphenyl, 3,5-dimethylphenyl, 3,6-dimethylphenyl, 2,4,6-trimethylphenyl, 3,4,5-trimethylphenyl, 2,3,4-trimethylphenyl, 2,4,5-trimethylphenyl, 2-methoxy-phenyl, 3-methoxy-phenyl, 4-methoxy-phenyl, 2,3-dimethoxy-phenyl, 2,4-dimethoxy-phenyl, 2,5-dimethoxy-phenyl, 2,6-dimethoxy-phenyl, 3,4-dimethoxy-phenyl, 3,5-dimethoxy-

phenyl, 3,6-dimethoxy-phenyl, 2-fluorophenyl, 3-fluorophenyl, 4-fluorophenyl, 2,3-difluorophenyl, 2,4-difluorophenyl, 2,5-difluorophenyl, 2,6-difluorophenyl, 3,4-difluorophenyl, 3,5-difluorophenyl, 3,6-difluorophenyl, 2-chlorophenyl, 3-chlorophenyl, 4-chlorophenyl, 2,3-dichlorophenyl, 2,4-dichlorophenyl, 2,5-dichlorophenyl, 2,6-dichlorophenyl, 3,4-dichlorophenyl, 3,5-dichlorophenyl, 3,6-dichlorophenyl, 2,4,6-trichlorophenyl, 3,4,5-trichlorophenyl, 2,3,4-trichlorophenyl, 2,4,5-trichlorophenyl, 2-bromophenyl, 3-bromophenyl, 4-bromophenyl, 2,3-dibromophenyl, 2,4-dibromophenyl, 2,5-dibromophenyl, 2,6-dibromophenyl, 3,4-dibromophenyl, 3,5-dibromophenyl, 3,6-dibromophenyl, 2-trifluoromethyl-phenyl, 3-trifluoromethyl-phenyl, 4-trifluoromethyl-phenyl, 2-cyano-phenyl, 3-cyano-phenyl, 4-cyano-phenyl, 2,3-di-cyano-phenyl, 2,4-di-cyano-phenyl, 2,5-di-cyano-phenyl, 2,6-di- cyano-phenyl, 3,4-di-cyano-phenyl, 3,5-di-cyano-phenyl, 3,6-di-cyano-phenyl, 2-nitro- phenyl, 3-nitro-phenyl, 4-nitro-phenyl, 2- (trifluoromethoxy) phenyl, 3- (trifluoromethoxy) phenyl, 4- (trifluoromethoxy) phenyl, 2- (phenyl) phenyl, 3- (phenyl) phenyl, 4- (phenyl) phenyl, 2- (hydroxymethyl) phenyl, 3- (hydroxymethyl) phenyl, 4- (hydroxymethyl) phenyl, 2- (2-pyridyl) phenyl, 3- (2-pyridyl) phenyl, 4- (2-pyridyl) phenyl, 2- (3-pyridyl) phenyl, 3- (3-pyridyl) phenyl, 4- (3-pyridyl) phenyl, 2- (4-pyridyl) phenyl, 3- (4-pyridyl) phenyl, 4- (4-pyridyl) phenyl, 2-chloro-4-fluorophenyl, 2-chloro-6-methyl-phenyl, 3-chloro-5-bromo-phenyl, 3-chloro- 5-propyl-phenyl, 3-chloro-5-methyl-phenyl, 3-chloro-5-ethyl-phenyl, 3-chloro-5-vinyl- phenyl, 3-chloro-5-allyl-phenyl, 3-chloro-5-phenyl-phenyl, 3-chloro-5- (hydroxymethyl)- phenyl, 3-chloro-5-cyano-phenyl, 3-chloro-5- (1, 2-propanediol)-phenyl, 2-naphthyl or 3-cyano-5-methyl. Preferred example for aryl in R2 is 3,5-dichlorophenyl.

Aryl in R3 is preferably an unsubstituted or substituted phenyl with suitable substituents selected from 1 to 5 substituents, preferably 1-4 substituents, more preferably 1-3 substituent selected from Cl 4-alkyl (preferable Cl 2-alkyl), Cl 4-alkoxy (preferable Cl-2-alkoxy), fluorine, chlorine, bromine, iodine and phenyl (preferably 1-3 substituent selected from Ci. 4-alkyl (preferable Cl-2-akl), Cl-4-alkoxy (preferable Cl 2-alkoxy) and halogen; more preferably 1-3 substituent selected from Cl 4-aLkyl (preferable Cl 2-alkyl) and Cl 4-alkoxy (preferable Cl 2-alkoxy). Examples of substituted aryl groups are 2-methyl-phenyl, 3-methyl-phenyl, 4-methyl-phenyl, 2-methoxy-phenyl, 3-methoxy- phenyl, 4-methoxy-phenyl, 2-chlorophenyl, 3-chlorophenyl, 4-chlorophenyl, 2,3-dichlorophenyl, 2,4-dichlorophenyl, 2,5-dichlorophenyl, 2,6-dichlorophenyl, 3,4-dichlorophenyl, 3,5-dichlorophenyl or 3,6-dichlorophenyl. Most preferred aryl in R3 is phenyl.

Aryl in R5, R'and R"is as defined above, preferably phenyl.

The term"heterocyclyl"as used herein denotes an optionally substituted saturated, partially unsaturated or aromatic monocyclic or bicyclic heterocycle which contains 1 to 4 hetero atoms selected from nitrogen, oxygen and sulfur which can also be fused to an optionally substituted saturated, partially unsaturated or aromatic monocyclic carbocycle or heterocycle.

Examples of suitable heterocycles are oxazolyl, isoxazolyl, furyl, tetrahydrofuryl, 1,3-dioxolanyl, dihydropyranyl, thienyl, pyrazinyl, isothiazolyl, isoquinolinyl, indolyl, indazolyl, quinolinyl, dihydrooxazolyl, pyrimidinyl, benzofuranyl, tetrazolyl, pyrrolidinyl, pyrrolidinonyl, (N-oxide)-pyridinyl, pyrrolyl, triazolyl e. g. 1,2,4-triazolyl, pyrazolyl, benzotriazolyl, piperidinyl, morpholinyl, thiazolyl, pyridyl, dihydrothiazolyl, imidazolidinyl, pyrazolinyl, benzothienyl, piperazinyl, imidazolyl, thiadiazolyl e. g.

1,2,3-thiadiazolyl, and benzothiazolyl. Most preferred example is pyridyl.

Heterocyclyl in Rl, R2 and R3 are preferably an unsubstituted or substituted pyridyl with suitable substituents selected from 1 to 5 of halogen, nitro and unsubstituted straight or branched chain alkyl containing 1 to 4 carbon atoms.

Suitable substituents for heterocyclyl can be selected from those named for alkyl, in addition however an oxo group (=O) as substituent can be added to the selection.

The term"C (=O) R"as used herein denotes an carbonyl group to which the following substituents are attached, wherein the substituents selected from hydrogen, alkyl, alkoxy, trifluoromethyl, methyl-oxy-carbonyl and ethyl-oxy-carbonyl (preferably hydrogen or alkyl). Examples for suitable substituents for the carbonyl group are hydrogen, tert.-butoxy, trifluoromethyl, methyl, ethyl-oxy-carbonyl. In an other embodiment of the invention preferred acyl groups are those wherein R is hydrogen or an unsubstituted straight or branched chain hydrocarbon residue containing 1 to 7 carbon atoms.

The term"CONR'R""as used herein denotes amides wherein R'and R", are independently of each other, hydrogen, alkyl or aryl (preferably hydrogen or Cl 7-alkyl (preferable Cl 4-alkyl)). Examples for suitable substituents for the amide group (R'and/or R") are hydrogen, C, 4-alkyl (preferably methyl), phenyl, 2,4,6-trimethoxy-benzyl.

Within the invention the term"X"represents S, S (O), S (0) 2, O, N (alkyl) or X-R2 together represent CH2-aryl (preferably CH2-phenyl) or CH2-heterocyclyl (preferably CH2- (4)-pyridyl, CH2- (3)-pyridyl, CH2- (2)-pyridyl), more preferable S, S (O), S (0) 2, O, N (alkyl) and most preferred the term"X"represents S.

The term halogen stands for fluorine, chlorine, bromine and iodine. Most preferred halogen is chlorine.

Any functional (i. e. reactive) group present in a side-chain may be protected, with the protecting group being a group which is known per se, for example, as described in "Protective Groups in Organic Synthesis", 2nd Ed., T. W. Greene and P. G. M. Wuts, John Wiley & Sons, New York, NY, 1991. For example, an amino group can be protected by tert.-butoxycarbonyl (BOC) or benzyloxycarbonyl (Z).

The compounds of this invention may contain one or more asymmetric carbon atoms and may therefore occur as racemates and racemic mixtures, single enantiomers, diastereomeric mixtures and individual diastereomers. Furthermore, where a compound of the invention contains an olefinic double bond, this can have the (E) or (Z) configuration. Also, each chiral center may be of the R or S configuration. All such isomeric forms of these compounds are embraced by the present invention.

Compounds of formula I which are acidic can form pharmaceutically acceptable salts with bases such as alkali metal hydroxides, e. g. sodium hydroxide and potassium hydroxide; alkaline earth metal hydroxides, e. g. calcium hydroxide, barium hydroxide and magnesium hydroxide, and the like; with organic bases e. g. N-ethyl piperidine, dibenzylamine, and the like. Those compounds of formula (I) which are basic can form pharmaceutically acceptable salts with inorganic acids, e. g. with hydrohalic acids such as hydrochloric acid and hydrobromic acid, sulphuric acid, nitric acid and phosphoric acid, and the like, and with organic acids, e. g. with acetic acid, tartaric acid, succinic acid, fumaric acid, maleic acid, malic acid, salicylic acid, citric acid, methanesulphonic acid and p-toluene sulphonic acid, and the like. The formation and isolation of such salts can be carried out according to methods known in the art.

A preferred embodiment of the invention are compounds of formula I wherein Rl is alkyl, preferably wherein R/is Ci-7 alkyi or C, 7 alkyl substituted with 1-3 substituents selected from cycloalkyl, aryl and heterocyclyl, more preferably wherein Rl is methyl, ethyl, isopropyl, cyclohexylmethyl, phenylmethyl, pyridylmethyl,

most preferably wherein Rl is 4-pyridylmethyl; Ra is alkyl or aryl, preferably wherein R2 is C1-7 alkyl, phenyl or phenyl substituted with 1-5 substituents selected from Cl-7 alkyl, halogen and nitro, more preferably wherein R2 is methyl, n-propyl or phenyl substituted with 1-5 chlorine atoms, most preferably wherein R2 is methyl or 3,5-dichlorophenyl; R3 is alkyl, cycloalkyl or aryl, preferably wherein R3 is Cl-7 alkyl, Cl-7 alkyl substituted with 1-3 heterocyclyl, phenyl or phenyl substituted with 1-5 substituents selected from Cl 4-alkyl, Cl 4-alkoxy and halogen; more preferably wherein R3 is isopropyl, n-propyl or pyridylmethyl, most preferably wherein R3 is isopropyl ; R4 is hydrogen, alkyl, carboxyl, C (=O) R, CONR'R", cyano or alkenyl, wherein R is hydrogen, alkyl, alkoxy, trifluoromethyl, methyl-oxy-carbonyl or ethyl-oxy- carbonyl, wherein R'and R", are independently of each other, hydrogen, alkyl or aryl, preferably wherein

R is hydrogen, C, 7 alkyl or Cl 7 alkyl substituted with 1-3 substituents selected from hydroxy, amino, C, 4-alkoxy, phenyl, methyl-oxy-carbonyl, ethyl-oxy-carbonyl, azido, 2- pyridyl-carbonyl-amino, 3-pyridyl-carbonyl-amino, 4-pyridyl-carbonyl-amino, (phenoxy)-carbonyl-amino, (methoxy)-carbonyl-amino, (di-methyl-amino)-carbonyl- amino, (phenyl-amino)-carbonyl-amino, (amino)-carbonyl-amino, (phenyl)-carbonyl- amino, (methyl)-carbonyl-amino, methyl-carbonyl-amino-methyl-carbonyl-amino, (tert.- butyl)-carbonyl-amino-methyl-carbonyl-amino, methyl-sulfonyl-amino, phenyl-sulfonyl- amino, p-toluyl-sulfonyl-amino, (N1-acetyl-O-tert.-butyl-N2-yl)-L-serinamide, (N1- acetyl-N2-yl)-L-serinamide and [Nl-(tert.-butoxycarbonyl)-O-tert.-butyl-N2-yl]-L- serinamide, more preferably wherein R4 is hydrogen or Cl-2 alkyl substituted with 1-3 substituents selected from hydroxy, amino, Cl-2-alkoxy, 2-pyridyl-carbonyl-amino, 3-pyridyl-carbonyl-amino, 4-pyridyl- carbonyl-amino, (phenoxy)-carbonyl-amino, (methoxy)-carbonyl-amino, (di-methyl- amino)-carbonyl-amino, (phenyl-amino)-carbonyl-amino, (amino)-carbonyl-amino, (phenyl)-carbonyl-amino, (methyl)-carbonyl-amino, methyl-carbonyl-amino-methyl- carbonyl-amino, (tert.-butyl)-carbonyl-amino-methyl-carbonyl-amino, (N1-acetyl-O- tert.-butyl-N2-yl)-L-serinamide, (Nl-acetyl-N2-yl)-L-serinamide and [Nl- (tert.- butoxycarbonyl)-O-tert.-butyl-N2-yl]-L-serinamide, most preferably wherein R4 is Cl-2 alkyl substituted with 1-2 substituents selected from hydroxy, 2-pyridyl- carbonyl-amino, 3-pyridyl-carbonyl-amino, 4-pyridyl-carbonyl-amino, (phenoxy)- carbonyl-amino, (methoxy)-carbonyl-amino, (di-methyl-amino)-carbonyl-amino, (phenyl-amino)-carbonyl-amino, (amino)-carbonyl-amino, (phenyl)-carbonyl-amino, (methyl)-carbonyl-amino, methyl-carbonyl-amino-methyl-carbonyl-amino, (tert.-butyl)- carbonyl-amino-methyl-carbonyl-amino, (N1-acetyl-O-tert.-butyl-N2-yl)-L-serinamide, (Nl-acetyl-N2-yl)-L-serinamide and [Nl- (tert.-butoxycarbonyl)-O-tert.-butyl-N2-yl]-L- serinamide; R5 is alkyl, aryl or a group-Z-C (=O) R"', wherein Z is a single bond or-CH=CH-, and R"'is hydrogen or alkyl, preferably wherein

R5 is C1-7 alkyl, phenyl, C1-7 alkyl substituted with 1-3 substituents selected from hydroxy, Cl-4-alkoxy, methyl-carbonyl-oxy and amino-carbonyl-oxy, more preferably wherein R5 is methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert.-butyl or Ci-2-alkyl substituted with 1-3 substituents selected from hydroxy, Cl-2-alkoxy, methyl- carbonyl-oxy and amino-carbonyl-oxy, most preferably wherein R5 is methyl, ethyl, n-propyl, isopropyl or Cl 2-alkyl substituted with 1-3 substituents. selected from hydroxy, methyl-carbonyl-oxy and amino-carbonyl-oxy; X represents S, O, N (alkyl) or X-R2 together represent CH2-aryl or CH2-heterocyclyl ; and with the proviso that alkyl in R3 is not CF3, preferably wherein X represents S.

Other preferred embodiments of the invention are compounds of formula I wherein Rl is alkyl, cycloalkyl, aryl or heterocyclyl, preferably wherein Rl is alkyl, more preferably wherein

Rl is alkyl substituted with heterocyclyl or aryl, unsubstituted C1-7 alkyl or alkyl substituted with cycloalkyl, most preferably wherein Rl is pyridylmethyl, phenylmethyl, methyl, ethyl, isopropyl, cyclohexylmethyl; Ra is alkyl, cycloalkyl, aryl or heterocyclyl, preferably wherein R2 is alkyl or aryl, more preferably wherein R2 is unsubstituted alkyl, unsubstituted phenyl or substituted phenyl with 1 to 5 halogen or nitro or unsubstituted C1-7 alkyl as substituents, most preferably wherein R2 is methyl, n-propyl or chlorinated phenyl; R3 is hydrogen, alkyl, cycloalkyl, aryl or heterocyclyl, preferably wherein R3 is alkyl or aryl, more preferably wherein R3 is unsubstituted alkyl or substituted alkyl with heterocyclyl as substituent, unsubstituted phenyl or substituted phenyl with 1 to 5 halogen or methoxy or unsubstituted alkyl as substituents, most preferably wherein R3 is isopropyl, n-propyl or pyridylmethyl; R4 is hydrogen, alkyl, carboxyl, C (=O) R or CONR2 wherein R is hydrogen or alkyl, preferably wherein

R4 is hydrogen, alkyl, carboxyl, C (=O) R or CONR2, more preferably wherein R4 is hydrogen, unsubstituted alkyl or substituted alkyl with hydroxy or amino or methoxy as substituents, carboxyl, C (=O) R, CONR2, most preferably wherein R4 is methyl or ethyl with hydroxy or methoxy as substituents, carboxyl, C (=O) R, CONR2 ; Rus ils hydrogen or alkyl, preferably wherein R5 is hydrogen, unsubstituted alkyl or substituted alkyl with hydroxy as substituent, more preferably wherein R5 is methyl or ethyl optionally substituted with a hydroxy group ; X represents S, S (O), S (0) 2, O, N (alkyl) or X-R2 together represent CH2-aryl or CH2-heterocyclyl ; and with the proviso that only one of R3, R4 and R5 is hydrogen and alkyl in R3 is not CF3, preferably wherein X represents S, S (O), S (0) 2, O, N (alkyl), more preferably wherein X represents S; hydrolyzable esters or ethers thereof or a pharmaceutically acceptable salt thereof.

Other preferred embodiments of the invention are compounds of formula I wherein Rl is 4-pyridyl methyl;

R2 is methyl or 3,5-dichlorophenyl; R3 is isopropyl ; R4 is methyl substituted with a hydroxy group or C (=O) R; R5 is methyl; X represents S.

More preferred embodiments of compounds of formula I, as well as hydrolyzable esters or ethers thereof or a pharmaceutically acceptable salt thereof, are listed in table 1 (seebelow): Table 1 STRUCTURE SYSTEMATIC NAME Cl/8 eN 5-(3, 5-Dichlorophenylthio)-4-isopropyl- ci 2-methyl-1- [ (4-pyridyl) methyl]-lH- N pyrrole-3-methanol < tOH OH ci IN 5- (3, 5-Dichlorophenylthio)-4-isopropyl- 9 eJJ 2-methyl-1-[(4-pyridyl) methyl]-1H- pyrrole-3-carboxaldehyde zozo 5- (3, 5-Dichlorophenylthio)-4-isopropyl- ci alpha (RS)-methyl-1- [ (4-pyridyl) methyl]- 1H-pyrrole-3-ethanol OH < fOH ci 5- (3, 5-Dichlorophenylthio)-4-isopropyl- ci j I 1, 2-dimethyl-lH-pyrrole-3-methanol s-t N OH cl cl -5- (3, 5-Dichlorophenylthio)-l-ethyl-4- td NC isopropyl-2-methyl-lH-pyrrole-3 methanol OH Cj ci 1-Benzyl-5- (3, 5-dicblorophenylthio)-4- isopropyl-2-methyl-lH-pyrrole-3- methanol OH CI 1- (Cyclohexylmethyl)-5- (3, 5- dichlorophenylthio)-4-isopropyl-2- 5aNr methyl-lH-pyrrole-3-methanol OH ci cl N 5- (3, 5-Dichlorophenylthio)-4-isopropyl- 9 S 2-methyl-l- [(2-pyridyl) methyl]-1H- N pyrrole-3-methanol OH 5- (3, 5-Dichlorophenylthio)-4-isopropyl- 9 C 2-methyl-l-[(3-pyridyl) methyl]-1H- N pyrrole-3-methanol OH 4-Isopropyl-2-methyl-5-phenylthio-l- [ (4- pyridyl) methyl]-1H-pyrrole-3-methanol N OH ci 5- (3-Chlorophenylthio)-4-isopropyl-2- 9 e) methyl-l- [(4-pyridyl) methyl]-1H- N pyrrole-3-methanol OH 4-Isopropyl-2-methyl-5- (3- 9 nJ nitrophenylthio)-1-[(4-pyridyl) methyl]- SÇt lH-pyrrole-3-methanol OH 5- (3, 5-Dimethylphenylthio)-4-isopropyl- 2-methyl-I- [ (4-pyridyl) methyl]-1H- N pyrrole-3-methanol OH 4-Isopropyl-5-isopropylthio-2-methyl-1- [ (4-pyridyl) methyl]-lH-pyrrole-3- methanol OH 4-Isopropyl-2-methyl-5-methylthio-1- [ (4-pyridyl) methyl]-1 H-pyrrole-3- N methanol OH 5- (3, 5-Dichlorophenylthio)-2-methyl-4- phenyl-1- [ (4-pyridyl) methyl]-1H- N pyrrole-3-methanol < OH OH 4- (4-Chlorophenyl)-5- (3, 5- cl dichlorophenylthio)-2-methyl-l- [ (4- pyridyl) methyl]-1H-pyrrole-3-methanol ON OH cl, N 5- (3, 5-Dichlorophenylthio)-2-methyl-4- ci (4-methylphenyl)-1- [ (4-pyridyl) methyl- s X lH-pyrrole-3-methanol OH v 5- (3, 5-Dichlorophenylthio)-4- (4- methoxyphenyl)-2-methyl-1- [ (4- \ t pyridyl) methyl]-lH-pyrrole-3-methanol OH -0 4- (3, 4-Dichlorophenyl)-5- (3, 5- dichlorophenylthio)-2-methyl-1- [ (4- \5 t pyridyl) methyl]-lH-pyrrole-3-methanol OH ci ci ci 5- (3, 5-Dichlorophenylthio)-4-isopropyl- cl 2-methyl-1- [ (4-pyridyl) methyl]-1H- pyrrole-3-carboxylic acid OH -cw ci ci 5- (3, 5-Dichlorophenylthio)-4-isopropyl- cl 2-methyl-1- [ (4-pyridyl) methyl]-1H- N pyrrole-3-carboxamide a FNH2 Nu2 cl | _ 4- [ [2- (3,5-Dichlorophenylthio)-3- cl isopropyl-4, 5-dimethyl-lH-pyrrol-1- N yl] methyl] pyridine cl t i _ 5-(3, 5-Dichlorophenylthio)-4-isopropyl- 2-methyl-1- [ (4-pyridyl) methyl]-1H- N pyrrole-3-methylamine v a tNH2 cl 4- [ [2- (3, 5-Dichlorophenylthio)-3- isopropyl-4- (methoxymethyl)-5-methyl- N 1H-pyrrol-1-yl] methyl] pyridine a °\ A ci ci 5- (3, 5-Dichlorophenylthio)-3- (hydroxymethyl)-4-isopropyl-1- [ (4- pyridyl) methyl]-lH-pyrrole-2-methanol oh OH ci 5- (3, 5-Dichlorophenylthio)-4-isopropyl- 1- [ (4-pyridyl) methyl]-lH-pyrrole-3- N methanol --OH 5- (3, 5-Dichlorophenylthio)-2-ethyl-4- w isopropyl-1- [ (4-pyridyl) methyl]-lH- N pyrrole-3-methanol OH 5- (3, 5-Dichlorophenoxy)-4-isopropyl-2- methyl-1- [ (4-pyridyl) methyl]-1H- o N pyrrole-3-methanol OH 5- [ (3, 5-Dichlorophenyl) methylamino]-4- cl isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-lH-pyrrole-3-methanol OH 5-Benzyl-4-isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-1H-pyrrole-3-methanol N OH 4-Isopropyl-2-methyl-1, 5-bis [ (4- 9 ß pyridyl) methyl]-lH-pyrrole-3-methanol ar N CL 5- (3, 5-Dichlorophenylthio)-l-isopropyl- 3-methyl-4- [ (4-pyridyl) methyl]-1H- N pyrrole-2-methanol OH j ci 5- (3, 5-Dichlorophenylthio)-4-isopropyl- ct N 1- [ (4-pyridyl) methyl]-1H-pyrrole-2- methanol OH Cl 8-5-(3, 5-Dichlorophenylthio)-4-isopropyl- / 3-methyl-1- [ (4-pyridyl) methyl]-1H- N pyrrole-2-methanol OH Cl 5- (3,5-Dichlorophenylthio)-2,4- cl (dimethyl-1- [ (4-pyridyl) methyl]-lH- N pyrrole-3-methanol / OH 5- (3, 5-Dichlorophenylthio)-4-isopropyl- 2-phenyl-l- [ (4-pyridyl) methyl]-lH- s pyrrole-3-methanol HO \ uo 5- (3, 5-Dichlorophenylthio)-4-isopropyl- W C 2-methyl-1-[(3-pyridyl) methyl]-1H- N pyrrole-3-methanol OH 5- (2-chloro-4-fluorophenylthio)-4- isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-lH-pyrrole-3-methanol cri mu .-ON 0 4-Isopropyl-5- (4-methoxyphenylthio)-2- methyl-1- [ (4-pyridyl) methyl]-1H- pyrrole-3-methanol 5 N OH 5- (2-Chlorophenylthio)-4-isopropyl-2- methyl-1- [ (4-pyridyl) methyl]-1H- pyrrole-3-methanol OH F F 5- [3- (Trifluoromethyl) phenylthio]-4- w N isopropyl-2-methyl-1- [ (4- \ N pyridyl) methyl]-lH-pyrrole-3-methanol Ar OH 5- [4- (Trifluoromethoxy) phenylthio]-4- o isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-1H-pyrrole-3-methanol 5 N OH 5- (2, 5-Dichlorophenylthio)-4-isopropyl- 2-methyl-1- [ (4-pyridyl) methyl]-lH- pyrrole-3-methanol OH 0'rN 5- (3, 5-Dichlorophenylthio)-2,4- / diisopropyl-l- [ (4-pyridyl) methyl]-1H- N pyrrole-3-methanol OH 4-Isopropyl-2-methyl-5- (2- naphthylthio)-l [ (4-pyridinyl) methyl]- 1H-pyrrole-3-methanol 5 N OH 5- (2, 4-Dichlorophenylthio)-4-isopropyl- 2-methyl-1- [ (4-pyridyl) methyl]-1H- cl pyrrole-3-methanol "''N OH ß OH 5- (3-Fluorophenylthio)-4-isopropyl-2- methyl-1- [ (4-pyridyl) methyl]-1H- N pyrrole-3-methanol OH > OH 5- (3-Chlorophenylthio)-2, 4-diisopropyl- 1- [ (4-pyridyl) methyl]-lH-pyrrole-3- methanol OH ~ 4-Isopropyl-5- (3, 4- N dimethoxyphenylthio)-2-methyl-1- [ (4- I X nJ pyridyl) methyl]-lH-pyrrole-3-methanol X \ HÓ 4-Isopropyl-2-methyl-5- (2, 4, 6- trimethylphenylthio)-1- [ (4- pyridyl) methyl]-lH-pyrrole-3-methanol Ar HO N 4-Isopropyl-2-methyl-5- (3, 4- dimethylphenylthio)-1- [ (4- pyridyl) methyl]-lH-pyrrole-3-methanol < \ HO 4-Isopropyl-5- (2, 5- dimethoxyphenylthio)-2-methyl-1- [ (4- pyridyl) methyl]-lH-pyrrole-3-methanol w/X HO 4-Isopropyl-2-methyl-5- (2, 5- tN<) dimethylphenylthio)-1- [ (4- N pyridyl) methyl]-lH-pyrrole-3-methanol H 4-Isopropyl-5- (2-methoxyphenylthio)-2- methyl-1- [ (4-pyridyl) methyl]-1H- 5 pyrrole-3-methanol HO 5- (2-Fluorophenylthio)-4-isopropyl-2- methyl-1- [ (4-pyridyl) methyl]-1H- F pyrrole-3-methanol HO 4-Isopropyl-2-methyl-5- (4- N methylphenylthio)-1- [ (4- pyridyl) methyl]-1H-pyrrole-3-methanol < \ HO 1-Benzyl-5- (3-chlorophenylthio)-4- el isopropyl-2-methyl-lH-pyrrole-3- methanol N HO \ HO v\g° 5- (3-Chlorophenylthio)-4-isopropyl-1- cl (4-methoxybenzyl)-2-methyl-lH- pyrrole-3-methanol s Ho 5- (3-Chlorophenylthio)-4-isopropyl-l- ci /"\ (3-methoxybenzyl)-2-methyl-lH- pyrrole-3-methanol HO HO CI 1- [ (5-Chloro-1-benzothiophen-3- yl) methyl]-5- (3-chlorophenylthio)-4- isopropyl-2-methyl-lH-pyrrole-3- methanol 5 N HO cl N alpha (RS)- [5- (3, 5-Dichlorophenylthio)- ci (P ) P Y 4-isopropyl-2-methyl-l- [ (4- pyridyl) methyl]-lH-pyrrol-3-yljbenzyl alcohol Ha N^5 5- (3-Chlorophenylthio)-4-isopropyl-2- methyl-1- [ (4-thiazolyl) methyl]-1H- pyrrole-3-methanol s Ho 5- (3-Chlorophenylthio)-4-isopropyl-2- methyl-l- [ (3- (4-pyridyl) propyll-lH- ci pyrrole-3-methanol X HO 5-(3-Chlorophenylthio)-4-isopropyl-2- methyl-l- [ (2-quinolyl) methyl]-1H- pyrrole-3-methanol 5 N HO \ 4-Isopropyl-2-methyl-5- (2,4- dimethylphenylthio)-l- [ (4- pyridyl) methyl]-lH-pyrrole-3-methanol N HO 4-Isopropyl-2-methyl-5- (3- methylphenylthio)-l- [ (4- pyridyl) methyl]-lH-pyrrole-3-methanol s HO 5- (2-Chloro-6-methylphenylthio)-4- isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-lH-pyrrole-3-methanol n \ Hg F 5- (3-Chlorophenylthio)-1- [ [4-chloro-2- N F (trifluoromethyl)-6-quinolyl] methyl]-4- ci isopropyl-2-methyl-1H-pyrrole-3- methanol Cl HO 5- (4-Ethylphenylthio)-4-isopropyl-2- methyl-1- [ (4-pyridyl) methyl]-1H- pyrrole-3-methanol 5 N HO 4-Isopropyl-5- (3-methoxyphenylthio)-2- methyl-1- [ (4-pyridyl) methyl]-1H- pyrrole-3-methanol 5 HO cl fN 5-(2, 4,6-Trichlorophenylthio)-4- isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-1H-pyrrole-3-methanol ci 5 \ I ci N-Benzyl-2- (3-chlorophenylthio)-4- (hydroxymethyl)-3-isopropyl-5-methyl- X SJ l-pyrroleacetamide c, 0 zozo 5 HO HA 5- (3-Chlorophenylthio)-1- [ [6- CRI 6f v (trifluoromethyl)-3-pyridyl] methyl]-4- zon isopropyl-2-methyl-lH-pyrrole-3- 5 N methanol HO ci ci [5- (3, 5-Dichloro-phenylsulfanyl)-4- ci isopropyl-2-methyl-l-pyridin-4- N ylmethyl-1H-pyrrol-3-yl]-hydroxy-acetic acid ethyl ester HO C1 N N- [ [5- (3, 5-Dichlorophenylthio)-4- 9 eJ isopropyl-2-methyl-1-[(4- pyridyl) methyl]-1H-pyrrol-3-yl] methyl]- 4-pyridineacetamide 0 O ci N 2-Acetamido-N- [ [5- (3, 5- ct 9 S dichlorophenylthio)-4-isopropyl-2- methyl-1- [ (4-pyridyl) methyl]-lH-pyrrol- 3-yl] methyl] acetamide ° Nd .. N- [ [5- (3, 5-Dichlorophenylthio)-4- ci isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-lH-pyrrol-3-yl] methyl]- p-toluenesulfonamide 0 cl tert.-butyl [ [ [ [5- (3, 5- dichlorophenylthio)-4-isopropyl-2- 5 N methyl-1- [ (4-pyridyl) methyl]-lH-pyrrol- b 3- yl] methyls carbamoyl methyl] carbamate o-- cl N2- [ [5- (3, 5-Dichlorophenylthio)-4- cl N isopropyl-2-methyl-I- [ (4- 5_ {NB pyridyl) methyl]-lH-pyrrol-3- yl] methyl] glycinamide o\NHz Cl N- [ [5- (3, 5-Dichlorophenylthio)-4- cl isopropyl-2-methyl-1- [ (4- pyridyl) methyl-lH-pyrrol-3- yl] methyl] methanesulfonamide b 0 ou- cl w er Phenyl [ [5- (3, 5-dichlorophenylthio)-4- isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-1H-pyrrol-3- yl] methyl] carbamate b Fob b Cl 8 eN Methyl [ [5- (3, 5-dichlorophenylthio)-4- isopropyl-2-methyl-l- [ (4- pyridyl) methyl]-lH-pyrrol-3- yl] methyl] carbamate zu ' 0 N- [ [5- (3,5-Dichlorophenylthio)-4- cl N isopropyl-2-methyl-l- [ (4- pyridyl) methyl]-1H-pyrrol-3- yl] methyl] benzenesulfonamide O-io 0=5 \/ 0 Chiral Nl-acetyl-O-tert.-butyl-N2- [ [5- (3, 5- cl dichlorophenylthio)-4-isopropyl-2- methyl-1- [ (4-pyridyl) methyl]-1H-pyrrol- 3-ylmethyl]-L-serinamide 0 0 t Cl/ » N Chiral Nl-acetyl-N2-[[5-(3, 5- cl dichlorophenylthio)-4-isopropyl-2- methyl-1- [ (4-pyridyl) methyl]-lH-pyrrol- 3-yl] methyl]-L-serinamide o HO Ho Nl- (tert.-butoxycarbonyl)-O-tert.-butyl- N2- [ [5- (3, 5-dichlorophenylthio)-4- 5 N < §4o isopropyl-2-methyl-1- [ (4- oU pyridyl) methyl]-lH-pyrrol-3-yl] methyl]- o/ L-serinamide ) r 1- [ [5- (3, 5-Dichlorophenylthio)-4- ci isopropyl-2-methyl-l- [ (4- pyridyl) methyl]-lH-pyrrol-3-yl] methyl]- 3, 3-dimethylurea oF \ 1- [ [5- (3, 5-Dichlorophenylthio)-4- cl isopropyl-2-methyl-1- [ (4-pyriyl) methyl]- 1H-pyrrol-3-yl] methyl]-3-methyl-3- phenylurea L cl 1- [ [5- (3, 5-Dichlorophenylthio)-4- cl N isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-lH-pyrrol-3- yl] methyl] urea NH2 \ -NH, CI cl"q ci 4- [ [2- (3, 5-Dichlorophenylthio)-3- isopropyl-4- (methoxymethyl)-5-methyl- 1-pyrrolyl] methyl] pyridine N \ 4- [ [2- (3-Chlorophenylthio)-3-isopropyl- 4- (methoxymethyl)-5-methyl-l- pyrrolyl] methyl] pyridine Eo\ Cl/8 eN 4-[[3-(Azidomethyl)-5-(3,5- dichlorophenylthio)-4-isopropyl-2- N methyl-1-pyrrolyl] methyl] pyridine N=Nt--N- Cl er N- [ [5- (3,5-Dichlorophenylthio)-4- e1 N isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-lH-pyrrol-3- yl] methyl] acetamide F o cl, N 4- [ [2- (3, 5-Dichlorophenylthio)-3- cl isopropyl-5-methyl-4-vinyl-l- pyrrolyllmethyllpyridine cl(RS)- [5- (3, 5-Dichlorophenylthio)-4- cl isopropyl-2-methyl-1- [ (4- N pyridyl) methyl]-1H-pyrrol-3-yl]-1, 2- ethanediol OH OH OH N- [ [5- (3, 5-Dichlorophenylthio)-4- cl isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-1H-pyrrol-3- XN yl] methyl] benzamide 0 Br/er tert.-butyl 5-(3-bromo-5- Br chlorophenylthio)-4-isopropyl-2-methyl- -q 1- [ (4-pyridyl) r4ethyll-lH-pyrrole-3- carboxylate o k o Br w f r tert.-butyl 5-(3,5-dibromophenylthio)-4- Br isopropyl-2-methyl-l- [ (4- pyridyl) methyl]-lH-pyrrole-3- carboxylate zozo o ci 1- [5- (3,5-Dichlorophenylthio)-4- cl " 9 eJ isopropyl-2-methyl-1-[(4- pyridyl) methyl]-lH-pyrrol-3-yl]-2, 2,2- trifluoroethanone F F 1- [5- (3, 5-Dichlorophenylthio)-4- cl W} e) isopropyl-2-methyl-1-[(4- pyridyl) methyl]-IH-pyrrol-3-yI] ethanone A óf 5- (3, 5-Dibromophenylthio)-4-isopropyl- Br 2-methyl-1- [ (4-pyridyl) methyl]-1H- N pyrrole-3-carboxamide NHZ 0 4-Isopropyl-5- (3, 5- dimethoxyphenylthio)-2-methyl-I- [ (4- pyridyl) methyl]-lH-pyrrole-3- carboxamide NH2 a 0e 5- (3-Bromo-5-chlorophenylthio)-4- 8r isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-1H-pyrrole-3- carboxamide f kNH2 Ethyl 5- (3, 5-dichlorophenylthio)-4- isopropyl-2-methyl-1- [ (4- N pyridyl) methyl]-lH-pyrrole-3-glyoxalate 0 .. 5- (3-Cyanophenylthio)-4-isopropyl-2- methyl-l- [ (4-pyridyl) methyl]-lH- N pyrrole-3-carboxamide a FNH2 5- (3-Chlorophenylthio)-2- 9 eJ (hydroxymethyl)-4-isopropyl-alpha (RS)- methyl-1- [ (4-pyridyl) methyl]-1H- OH pyrrole-3-ethanol HO ci 5- (3, 5-Dichlorophenylthio)-3- (hydroxymethyl)-4-isopropyl-l- [ (4- pyridyl) methyl]-lH-pyrrole-2- /yo carboxaldehyde OH ci 5- (3, 5-Dichlorophenylthio)-4-isopropyl- 1- [ (4-py-ridyl) methyl]-IH-pyrrole-2, 3- dicarboxaldehyde d ° 5- (3, 5-Dichlorophenylthio)-3- (hydroxymethyl)-4-isopropyl-alpha (RS)- N methyl-1- [ (4-pyridyl) methyl]-1H- pyrrole-2-ethanol OH ci__qcl N 5- (3, 5-Dichlorophenylthio)-4-isopropyl- 1- [ (3-pyridyl] methyl]-IH-pyrrole-2, 3- dimethanol OH ow OH ci ci 5- (3, 5-Dichlorophenylthio)-4-isopropyl- -q I- [ (4-pyridyl) methyl]-IH-pyrrole-2- methanol OH ci [5- (3, 5-Dichlorophenylthio)-4-isopropyl- 1- [ (4-pyridyl) methyl]-lH-pyrrol-2- \oA yl] methyl acetate cl "< 5- (3, 5-Dichlorophenylthio)-4-isopropyl- 1- [ (4-pyridyl) methyll-1H-pyrrole-2- carbaldehyde a ci 4- [5- (3, 5-Dichloro-phenylsulfanyl)-4- cl isopropyl-1-pyridin-4-ylmethyl-1H- pyrrol-2-yl]-but-3-en-2-one a ci 4- [ [2- (3, 5-Dicblorophenylthio)-5- methyl-3-phenyl-l- pyrrolyl] methyl] pyridine cl W 4- [ [2- (3, 5-Dichlorophenylthio)-3-. isopropyl-5-methyl-l- pyrrolyl] methyl] pyridine CRI 5- (3, 5-Dichlorophenylthio)-N- (2, 4,6- trimethoxybenzyl)-2-methyl-4-phenyl-1- [ (4-pyridyl) methyl]-lH-pyrrole-3- o carboxamide d v/v °\ Cl 8 eN 5-(3, 5-Dichlorophenylthio)-2-methyl-4- phenyl-1- [ (4-pyridyl) methyl]-1H- 0 pyrrole-3-carboxylicacidtrifluoroacetate OH (1: 1) F. OH O/ Cl eN 5-(3, 5-Dichlorophenylthio)-4-phenyl-2- ci methyl-1- [ (4-pyridyl) methyl]-1H- N pyrrole-3-carboxamide v O ci 5- (3, 5-Dichlorophenylthio)-2-methyl-4- ci phenyl-l- [ (4-pyridyl) methyl]-1H- pyrrole-3-carbonitrile \N cl 5- (3, 5-Dichlorophenylthio)-4-isopropyl- N, 2-dimethyl-1- [ (4-pyridyl) methyl]-1H- N pyrrole-3-carboxamide H 0 5- (3, 5-Dichlorophenylthio)-4- cl cyclopropyl-2-methyl-1- [ (4- N pyridyl) methyl]-lH-pyrrole-3- carboxamide NH2 OU 5- (3, 5-Dichlorophenylthio)-4-isopropyl- 2-methyl-I- [ (4-pyridyl) methyl]-1H- N pyrrole-3-carboxanilide 4r W I cl w er 5-(3, 5-Dichlorophenylthio)-4-isopropyl- cl w 9 e) N, N, 2-trimethyl-1- [ (4-pyridyl) methyl- N 1H-pyrrole-3-carboxamide cl 5- (3-Allyl-5-chlorophenylthio)-4- L/- r N isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-lH-pyrrole-3- s carboxamide a 0F OU 5- (3-Chloro-5-propylphenylthio)-4- isopropyl-2-methyl-I- [ (4- pyridyl) methyl]-lH-pyrrole-3- s carboxamide ),.-NHZ o N 5- (3-Chloro-5-vinylphenylthio)-4- isopropyl-2-methyl-l- [ (4- pyridyl) methyl]-lH-pyrrole-3- carboxamide ~< FNH2 HO 5- [3-Chloro-5- (2 (RS), 3- OU , N dihydroxypropyl) phenylthio]-4- 9 e) isopropyl-2-methyl-1- [(4- pyridyl) methyl]-1H-pyrrole-3- s carboxamide NH2 OU ci 4- [ [2- (3, 5-Dichlorophenylthio)-5- cul (ethoxymethyl)-3-isopropyl-l- N pyrrolyl] methyls pyridine N 4- [ [2- (3, 5-Dichlorophenylthio)-3- roll isopropyl-5- (methoxymethyl)-l- N pyrrolyl) methyl] pyridine ß ci [5- (3, 5-Dichlorophenylthio)-4-isopropyl- c 1- [ (4-pyridyl) methyl]-lH-pyrrol-2- N yllmethyl carbamate \/°NHz Br ci 4-[[2-(3-Bromo-5-chlorophenylthio)-3- Br isopropyl-5-methyl-1- N pyrrolyl] methyl] pyridine cl, N 4- [ [2- (3-Allyl-5-chlorophenylthio)-3- /< r N isopropyl-5-methyl- [ (4- pyrrolyl] methyl] pyridine < cl 4- [ [2- (3-Chloro-5-propylphenylthio)-3- L/ f N isopropyl-S-methyl-1- / pyrrolyl] methyl] pyridine Cl 5- (3-Chloro-5-ethylphenylthio)-4- 9 e) isopropyl-2-methyl-1-[(4- pyridyl) methyl]-lH-pyrrole-3- carboxamide NH2 O HO ci 5- [3-Chloro-5- w N (hydroxymethyl) phenylthio]-4- isopropyl-2-methyl-1- [ (4- X} ~ pyridyl) methyl]-lH-pyrrole-3- NH2 carboxamide \ ó' 5- (2-Biphenylylthio)-4-isopropyl-2- v e) methyl-1- [(4-pyridyl) methyl]-lH-pyrrol- N 3-methanol HO 5- (3-Biphenylylthio)-4-isopropyl-2- methyl-1- [ (4-pyridyl) methyl] 1H- pyrrole-3-methanol N bd 4-Isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-5- [2- (3- pyridyl) phenylthioJ-lH-pyrrole-3- methanol N HO 5- [2- (Hydroxymethyl) phenylthio]-4- isopropyl-2-methyl-1- [ (4- Nô pyridyl) methyl]-1H-pyrrole-3-methanol HO \ HO /1 c, N 5- (5-Chloro-3-biphenylylthio)-4- isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-1H-pyrrole-3- carboxamide NH2 O 3-Chloro-5- [3-isopropyl-5-methyl-l- [ (4- 9 e) pyridinylmethyl]-lH-pyrrol-2- N ylthio] benzonitrile 5- [3-Isopropyl-5-methyl-1- [ (4- pyridyl) methyl]-1H-pyrrol-2-ylthio]-1, 3- dibenzonitrile I I

The compounds of formula I and hydrolyzable esters or ethers thereof or a pharmaceutically acceptable salt thereof are inhibitors of the human immunodeficiency virus reverse transcriptase enzyme both in vitro and in vivo, and can be used in the control or prevention of diseases mediated by the human immunodeficiency virus (HIV).

The pyrrole derivatives provided by the present invention are useful in therapeutic treatment of the human or animal body.

The pyrrole derivatives provided by the present invention are inhibitors of the human immunodeficiency virus reverse transcriptase enzyme. Accordingly, the present pyrrole derivatives are therapeutically active substances in the treatment of diseases mediated by the human immunodeficiency virus (HIV) and can be used as medicaments for the treatment of such diseases.

They can be used as medicaments, especially for treating viral diseases, immune mediated conditions or diseases, bacterial diseases, parasitic diseases, inflammatory diseases, hyperproliferative vascular diseases, tumors, and cancer.

In particular, compounds of the present invention and pharmaceutical compositions containing the same are useful as chemotherapeutic agents, inhibitors of viral replication and modulators of the immune system, and can be used for the treatment of diseases mediated by the human immunodeficiency virus (HIV) other viral diseases such as retroviral infections (either alone or in combination with other antiviral agents such as interferon or derivatives thereof, such as conjugates with polyethylene glycol).

They can be used alone, or in combination with other therapeutically active agents, for example, an immunosuppressant, a chemotherapeutic agent, an anti-viral agent, an antibiotic, an anti-parasitic agent, an anti-inflammatory agent, an anti-fungal agent and/or an anti-vascular hyperproliferation agent.

Compounds, whenever prepared by the processes of the present invention are also an object of the present invention.

The compounds of the present invention can be prepared as shown in the following scheme.

Reaction scheme 1: wherein Rl, R2, R3'R5 and R are as defined for compounds of formula I and and Prot is an amino protecting group.

In accordance with the present invention, compounds of formula VIII are prepared by reacting the compound of formula VII wherein R, R3 and R5 are as described in formula I with a iodination agent to obtain the iodo pyrrole derivative of formula VIII

wherein R, R3 and R5 are as described in formula I.

The iodination agent used for this reaction are known in the art and are for example N-iodosuccinimide, iodic acid in the presence of iodine, iodine in the presence of potassium iodide or sodium iodide, potassium iodide or sodium iodide in the presence of hydrogen peroxide.

The reactions can be carried out in a conventional manner known to the skilled in the art.

In Reaction scheme I, N-protected glycine (commercially available from Fluka) of formula II is reacted with N, O-dimethylhydroxylamine hydrochloride in the presence of N-ethylmorpholine and N-ethyl-N'- (3-dimethylaminopropyl) carbodiimide hydrochloride under nitrogen atmosphere. The term"amino protecting group" (Prot) as used herein refers to groups such as those employed in peptide chemistry such as a tert.- butoxycarbonyl group (t-BOC) or a benzyloxycarbonyl group (Z). Preferred amino protecting group (Prot) for this reaction is a tert.-butoxycarbonyl group. The reaction is conveniently carried out at a reaction temperature from 0°C to room temperature in an inert solvent, for example halogenated hydrocarbons such as anhydrous dichloromethane or polar aprotic solvents such as N, N-dimethylformamide (DMF) or tetrahydrofuran (THF) preferably dichloromethane, to yield the N-protected glycine N-methyl-N- methoxyamide of formula III.

The N-protected glycine N-methyl-N-methoxyamide of formula III is converted to the compound of formula IV by reaction with a Grignard reagent of the formula R3MgX (commercially available or synthesized according to methods known from textbooks on organic chemistry e. g. from J. March (1992),"Advanced Organic Chemistry: Reactions,

Mechanisms, and Structure", 4th ed. John Wiley & Sons) wherein R3 is as defined above but not hydrogen (for R3 being hydrogen, the reaction sequence starts with compound of the formula V; see below) and X represents a halogen for example chlorine. The reaction is conveniently carried out in an inert solvent, for example ethers such as anhydrous tetrahydrofuran, diethyl ether, dioxane or a mixture of the mentioned solvents at a reaction temperature from 0°C to room temperature. After the reaction, the Grignard product is worked-up in a manner known in the art for example with a solution of diluted hydrochloric acid, to yield the N-protected a-amino ketone of formula IV.

In the next step of the reaction, the N-protected oc-amino ketone of formula IV is reacted with trifluoroacetic acid or with hydrogen chloride thereby obtaining the deprotected a-amino ketone of formula V. In forming the compound of formula V, any conventional method for deprotection reactions of protected amino groups can be utilized in carrying out this reaction. The deprotection reaction of the compounds of formula IV is preferably carried out with trifluoroacetic acid optionally dissolved in dichloromethane or hydrogen chloride dissolved in ethyl acetate, dioxane or methanol at a reaction temperature from 0°C to room temperature. Most preferred, the deprotection reaction is carried out with hydrogen chloride dissolved in ethyl acetate.

The a-amino ketone of formula V is coupled with a (3-keto ester of the formula VI wherein R5 and R are as defined above (commercially available or synthesized according to methods known from textbooks on heterocyclic chemistry or organic chemistry e. g. from J. March (1992),"Advanced Organic Chemistry: Reactions, Mechanisms, and Structure", 46 ed. John Wiley & Sons) to form a pyrrole derivative of the formula VII. The synthesis of the pyrrole derivatives according to the Knorr synthesis of the formula VII is carried out in a manner known in the art. The reaction of the compounds of formula V and VI to yield compounds of the formula VII is preferably carried out with a mixture of potassium hydroxide and K2HPO4 in water at a reaction temperature from 20 to 40°C. Most preferred, the reaction is carried out with a mixture of ethyl acetoacetate, sodium acetate and acetic acid at a reaction temperature from 70 to 100°C.

In the next step of the reaction, an iodo pyrrole derivative of formula VIII is formed by the reaction of pyrrole derivative of the formula VII with an iodination agent. The iodination agent used for this reaction is known in the art and are for example N- iodosuccinimide, iodic acid in the presence of iodine, iodine in the presence of potassium iodide or sodium iodide, potassium iodide or sodium iodide in the presence of hydrogen peroxide. The reaction is for example carried out in an inert solvent, such as ethers, hydrocarbons or halogenated hydrocarbons preferably anhydrous dichloromethane at a reaction temperature from 0 to 40°C, preferably at room temperature in the presence of a iodination agent for example N-iodosuccinimide to yield the iodo pyrrole derivative of

formula VIII. After the reaction, the product is worked-up in a manner known in the art for example the mixture is washed with an aqueous solution of sodium thiosulphate and an aqueous solution of sodium hydrogen carbonate, dried over anhydrous sodium sulphate and finally the organic solvent was evaporated. The reaction is known in the literature for example from textbooks on organic chemistry e. g. J. March (1992), "Advanced Organic Chemistry: Reactions, Mechanisms, and Structure", 4th ed. John Wiley & Sons or as described in Y. Murata, Bull. Chem. Soc. Jpn. 1996 (11), 3339. The use of above-mentioned iodination agents is described for example in Synthesis 1995 (12), 1480, Tetrahedron 1992 (48) 44,9661 or Liebigs Ann. Chem. 1989 (9), 863.

The iodo pyrrole derivatives of formula VIII are converted to the corresponding pyrrole thio compounds of formula IX by reaction with a disulphide compound of the formula R2SSR2 or by the reaction with a compound of the formula R2SX wherein R2 is as defined above and X is a halogen, preferably chlorine (the compounds of the formula R2SSR2 and R2SX are commercially available or can be synthesized according to methods known from the art for example as described in US 4,282,242). The reaction is conveniently carried out by treating the compound of formula VIII under nitrogen atmosphere with a strong base for example sodium hydride or preferably lithium hydride, in an inert solvent for example anhydrous dimethyl sulphoxide at a reaction temperature from 0°C to room temperature and then reacting the mixture with the compounds of the formula R2SX or preferably with the disulphide compound of the formula R2SSR2. The reaction is preferably carried out at a reaction temperature from 40 to 60°C, yielding the compound of formula IX. After the reaction, the product is worked-up in a manner known in the art for example extracted with diethyl ether, dried over anhydrous magnesium sulphate and finally the organic solvent is evaporated.

In the next step of the reaction, the compound of formula IX is reacted with a compound of the formula RlX wherein Rl is as defined above but not hydrogen (the compound for Rl being hydrogen has already been described; see compound IX) and X represents a halogen for example bromo (commercially available or synthesized according to methods known from textbooks on organic chemistry e. g. from J. March (1992), "Advanced Organic Chemistry: Reactions, Mechanisms, and Structure", 4th ed. John Wiley & Sons) to obtain the N-substituted compound of the formula XI. In forming the compound of formula XI, any conventional method of substitution can be utilized in carrying out this reaction. The reaction of the compounds of formulas IX is preferably carried out under nitrogen in an inert solvent for example polar aprotic solvents such as tetrahydrofuran (THF) or N, N-dimethylformamide (DMF), preferably anhydrous THF at a temperature from 0°C to room temperature in the presence of tetra-n-butylammonium bromide and in the presence of a base such as sodium hydroxide, potassium carbonate,

sodium hydride or an amine of the formula R3N wherein R is methyl, ethyl or propyl.

Most preferred base is sodium hydroxide. Finally the mixture is reacted with the compound of the formula RlX to obtain the compound of formula XI.

The conversion of a compound of the formula XI to a compound of the formula Ia wherein R, Rl, R2, R3 and Rsare as defined above and R4 is CH20H and X represents S, is carried in that the compound of formula XI is reduced to the compound of formula la by reacting it with a reducing agent such as lithium aluminium hydride. The reaction is conveniently carried out by treating the compound of formula XI under nitrogen atmosphere with a reducing agent for example LiAIH4, LiBH4, BH3*S (CH3) 2, iso-Bu2AlH or Vitride@, in an inert solvent such as ethers for example anhydrous diethyl ether, THF of dioxane at a reaction temperature from 0°C to room temperature. Preferably, the reaction is carried out with LiAIH4 and ethers. Then a solution of ammonium chloride is added to yield to a compound of the formula Ia. After the reaction, the product is worked-up in a manner known in the art for example extracted with ethyl acetate, dried over anhydrous magnesium sulphate and finally the organic solvent is evaporated.

Oxidation of a compound of the formula Ia to a compound of the formula Ib wherein R, Rl, R2, R3 and Ware as defined above, R4 is C (=O) H and X represents S, is carried in that the compound of formula Ia is oxidized with an oxidizing reagent such iodobenzene diacetate in the presence of 2, 2,6,6-tetramethylpiperidine N-oxide, (COCI) 2 in the presence of dimethyl sulfoxide (DMSO), pyridinium chlorochromate in dichloromethane or MnO2 in ethers such as diethyl ether or in a halogenated hydrocarbons such as anhydrous dichloromethane or trichloromethane or in an aprotic polar solvent such as acetone and a compound of the formula Ib is obtained. The reaction is conveniently carried out by treating the compound of formula Ia under nitrogen atmosphere with an oxidizing agent, preferably iodobenzene diacetate and 2,2,6,6-tetramethylpiperidine N-oxide, in an inert solvent for example anhydrous dichloromethane at a reaction temperature from 0°C to room temperature to yield to a compound of the formula Ib. After the reaction, the product is worked-up in a manner known in the art for example washed with solutions of sodium thiosulphate and sodium hydrogen carbonate dried over anhydrous sodium sulphate and finally the organic solvent is evaporated.

Conversion of a compound of the formula Ib to a compound of the formula Ic wherein R, R, R2, R3 and R5are as defined above and R4 is CH (R) OH and X represents S, is carried in that the compound of formula Ib is reacted with a Grignard reagent of the formula RMgX or a reagent of the formula RLi (both compounds are commercially available or can be synthesized according to methods known from textbooks on organic chemistry e. g. from J. March (1992),"Advanced Organic Chemistry: Reactions,

Mechanisms, and Structure", 4th ed. John Wiley & Sons) wherein R is as defined above but not hydrogen (for R being hydrogen, the synthesis has already been described; see compound of the formula Ia) and X represents a halogen for example bromo to yield to a compound of the formula Ic. The reaction is conveniently carried out by treating the compound of formula Ib under nitrogen atmosphere, in an inert solvent for example ethers such as anhydrous tetrahydrofuran (THF), diethyl ether or dioxane, preferably THF with a Grignard reagent of the formula RMgX, preferably methyl magnesium bromide at a reaction temperature from 0°C to room temperature and then a solution of ammonium chloride is added to yield to a compound of the formula Ib. After the reaction, the product is worked-up in a manner known in the art for example extracted with ethyl acetate dried over anhydrous magnesium sulphate and finally the organic solvent is evaporated.

Compounds of the formula Ia wherein R, Rl, R2, R3 and R5are as defined above, R4 is hydrogen and X represents S, are synthesized according to known methods from the art.

For example the ester compounds of the formula XI are hydrolysed to the corresponding carboxylic acid according to methods known in the literature for example from textbooks on organic chemistry e. g. J. March (1992),"Advanced Organic Chemistry: Reactions, Mechanisms, and Structure", 4th ed. John Wiley & Sons. In a second step carboxylic acid function of the pyrrole derivative is then decarboxylated according to methods known in the art and for example described in S. F. Macdonald, J. Chem. Soc. 1952,4176 or G.

Kleinspehn, J. Am. Chem. Soc. 1954,76,5641.

Compounds of the formula Ia wherein R, Ri, R2, R3 and R5are as defined above, R4 is alkyl and X represents S, are synthesized according to known methods from the art. For example the compounds can be synthesised through elimination reaction of a compound of the formula Ic in a two step reaction, first in the presence of CH3SO2C1 and Et3N and secondly with a base such as potassium hydroxide or sodium hydroxide to form the corresponding alkenyl compound which is subsequently hydrogenated in the presence of hydrogen and palladium on activated coal (Pd/C) to the corresponding alkyl substituted pyrrole derivative. The reaction are all known in the literature for example from textbooks on organic chemistry e. g. J. March (1992),"Advanced Organic Chemistry: Reactions, Mechanisms, and Structure", 4th ed. John Wiley & Sons.

Compound of the formula I wherein R, Rl, R2, R3 and Rsare as defined above and R4 is C (=O) R wherein R is alkyl are synthesized according to known methods from the art.

For example, the hydroxy compounds of the formula Ic are oxidised according to methods known from the art for example from textbooks on organic chemistry e. g. from J. March (1992),"Advanced Organic Chemistry: Reactions, Mechanisms, and Structure", 4 th ed.

John Wiley & Sons) to obtain the corresponding oxo derivatives.

Compounds of the formula I wherein R, Rl, R2, R3 and R5are as defined above and is CONR2 are synthesized according to known methods from the art. For example, the ester compounds of the formula XI is hydrolysed as described above, then reacted with thionyl chloride to obtain the activated acid chloride and finally reacted with a compound of the formula HNR2 wherein R is hydrogen or alkyl to obtain the corresponding amide derivative. The reaction are all known in the literature for example from textbooks on organic chemistry e. g. J. March (1992),"Advanced Organic Chemistry: Reactions, Mechanisms, and Structure", 4 ed. John Wiley & Sons.

Compounds of the formula I wherein R, RI, R2, R3 R4 and Rare as defined above and X is S (O) or S (0) 2 are synthesized according to known methods from the art. For example, the compounds of the formula I, Ia, Ib or Ic are oxidized, to obtain the corresponding oxidised thio compounds derivatives. The reaction is known in the literature for example from textbooks on organic chemistry e. g. J. March (1992), "Advanced Organic Chemistry: Reactions, Mechanisms, and Structure", 4th ed. John Wiley & Sons.

Compounds of the formula I wherein R, Rl, R2, R3 R4 and Ware as defined above and X is O or N (alkyl) are synthesized according to known methods from the art. For example, the compounds of the formula VII are reacted with N-bromosuccinimide (NBS) to obtain the corresponding 2-substituted bromopyrrole which is further reacted with a neutral oxygen nucleophile, such as 3-methoxyphenol in the presence of Et3N to obtain the corresponding oxy pyrrole derivative. To obtain the corresponding N-substituted pyrrole derivatives, the above-mentioned 2-substituted bromopyrrole is reacted with a secondary amine in a polar aprotic solvent such as N, N-dimethylformamide (DMF). The reactions are all known in the literature for example from textbooks on organic chemistry e. g. J.

March (1992),"Advanced Organic Chemistry: Reactions, Mechanisms, and Structure", 4th ed. John Wiley & Sons or G. Cirrincione et al., Synthesis, 1997,1169.

Compounds of the formula I wherein R, Rl, R2, R3 R4 and R5are as defined above and X-R2 together represent CH2-aryl or CH2-heterocyclyl are synthesized according to known methods from the art. For example, compounds of the formula Va wherein R3 is as defined above and X-R together represent CH2-aryl or CH2-heterocyclyl are coupled with a P-keto ester of the formula VI wherein R5 and R are as defined above

(commercially available or synthesized according to methods known from textbooks on heterocyclic chemistry or organic chemistry e. g. from J. March (1992),"Advanced Organic Chemistry: Reactions, Mechanisms, and Structure", 4th ed. John Wiley & Sons) to form a pyrrole derivative of the formula VIIa wherein R, R3, R5 and X-R2 are as defined above. The synthesis of the pyrrole derivatives according to the Knorr synthesis of the formula VIIa is carried out in a manner known in the art. Subsequently the compound of the formula VIIa is further reacted according the above-described reactions starting with compound IX#XI#Ia#Ib#Ic.

The compounds of formula VIII are new intermediates and therefore also subject of the present invention.

Reaction scheme 2: wherein Rl, R2, R3'and R5 are as defined for compounds of formula I, R6 is Cl 4-alkyl and R taken together with the amino-methyl group is 2-pyridyl-carbonyl-amino-methyl, 3-pyridyl-carbonyl-amino-methyl, 4-pyridyl-carbonyl-amino-methyl, (amino-methyl)-

carbonyl-amino-methyl, (phenoxy)-carbonyl-amino-methyl, (methoxy)-carbonyl-amino- methyl, (di-methyl-amino)-carbonyl-amino-methyl, (phenyl-amino)-carbonyl-amino- methyl, (amino)-carbonyl-amino-methyl, (phenyl)-carbonyl-amino-methyl, (methyl)- carbonyl-amino-methyl, methyl-carbonyl-amino-methyl-carbonyl-amino-methyl, (tert.- butyl)-carbonyl-amino-methyl-carbonyl-amino-methyl, (Nl-Acetyl-O-tert.-butyl-N2- ylmethyl)-L-serinamide, (Nl-Acetyl-N2-yl] methyl)-L-serinamide, [N1- (tert.- butoxycarbonyl)-O-tert.-butyl-N2-yl-methyl]-L-serinamide, methyl-sulfonyl-amino- methyl, phenyl-sulfonyl-amino-methyl or p-toluyl-sulfonyl-amino-methyl.

The primary alcohol I-a may be alkylated, acylated or reacted with isocyanates to give carbamates according to methods known from textbooks on organic chemistry e. g. from J. March (1992),"Advanced Organic Chemistry: Reactions, Mechanisms, and Structure", 4th ed. John Wiley & Sons. These are standard reactions of which there are many combinations of reagents, for example, alkylation may be achieved using alkyl iodides, bromides, chlorides, triflates or any other suitable leaving group. Acylation may be achieved via acid chlorides or other activated carbonyl compounds such as activated carboxylic acids. Carbamates are accessible by reacting I-a with isocyanates in a standard procedure.

I-a may be further derivatised to the azide I-e using sodium azide or diphenylphosphoryl azide in standard procedures according to methods known from textbooks on organic chemistry e. g. from J. March (1992),"Advanced Organic Chemistry: Reactions, Mechanisms, and Structure", 4th ed. John Wiley & Sons.. I-e may be reduced to the primary amine I-f using hydrogenation with standard catalysts such as 10% palladium on carbon in suitable solvents, such as ethyl acetate, methanol or ethanol, or with a trialkyl or aryl phosphine.

The primary amine 1-f may be alkylated, acylated, sulfonylated or reacted with isocyanates (to give ureas) to give I-g according to methods known from textbooks on organic chemistry e. g. from J. March (1992),"Advanced Organic Chemistry: Reactions, Mechanisms, and Structure", 4th ed. John Wiley & Sons. These are standard reactions of which there are many combinations of reagents, for example, alkylation may be achieved using alkyl iodides, bromides, chlorides, triflates or any other suitable leaving group.

Acylation may be achieved via acid chlorides or other activated carbonyl compounds such as activated carboxylic acids. Sulfonylation may be via sulfonyl chlorides using a base such as triethylamine, N-methyl morpholine or N-ethyl morpholine. All these reactions may be

conducted in suitable solvents known to those skilled in the art, for example, dichloromethane, chloroform, dioxane, dimethyformamide, tetrahydrofuran, etc.

Ureas are accessible by reacting I-f with isocyanates in a standard procedure.

Derivatives of ester XI (reaction scheme 1), where the ester is replaced by other carbonyl groups (see reaction scheme 3), may be prepared according to reaction scheme 1 where the only change is intermediate VI for intermediate XII: Reaction scheme 3 (additional reagents of type VI): according to, Rs O O N R5 reaction scheme 1 s I R5 CIH. H2N + RSRsa- Ra Rsa Rs Rsa XVIII 1-h xiii i-h wherein Rl, W and R3 are as defined for compounds of formula I, where R5 is alkyl and R5a is hydrogen, amino, alkyl, alkoxy, trifluoromethyl, methyl-oxy-carbonyl or ethyl-oxy- carbonyl.

The chemistry to form the pyrrole and the subsequent reactions are as for those reactions already described in reaction scheme 1.

When R5a = methyl, yet further derivatives of the pyrrole may be prepared according to reaction scheme 4: Reaction scheme 4:

wherein Rl, R2, R3, and R5 are as defined for compounds of formula I.

I-h, prepared according to reaction scheme 3, may be reduced to the ethanol derivative I-i as already described. Elimination of water to form the vinyl compound I-j is achieved thermally by heating in a high boiling solvent such as DMSO, DMF, N-methyl pyrrolidinone, etc. Conversion of I-j into diol I-k may be achieved with osmium tetroxide, a standard reaction according to methods known from textbooks on organic chemistry e. g. from J. March (1992),"Advanced Organic Chemistry: Reactions, Mechanisms, and Structure", 4th ed. John Wiley & Sons.

Ketone reduction of I-1 (when R5a = COCOOEt) to form I-m is achieved using the same chemistry as for preparation of I-i : Reaction scheme 5: 1-1 I-m made via intermediate XII (reaction scheme 3) according to reaction scheme 1 wherein R', R2, R3'and R5 are as defined for compounds of formula I.

The pyrrole may also be constructed using a cycloaddition reaction according to the method of Yavari, Synthetic Communications, 1996,4495-4500 (reaction scheme 6).

Reaction scheme 6: H according to R' 3 co 2Et N CC) Et reaction scheme 1 1 ZS N C02Et 0 R C02Et et et R3 CO Et fiv xi xi FIV S N R R2.-S N NOme R2/C02H R Cet R C02Et 2. S N XVIII I R3 , OH I-n I-n R R N 2,, S_NC N R R3/7oH I-o I-p

wherein Rl, R2 and R3 are as defined for compounds of formula I.

In reaction scheme 6, the amino ketone V is reacted with diethylacetylene dicarboxylate of formula XIV in sodium acetate in refluxing ethanol to give an intermediate which is cyclised with acid giving XV. Other acetylenic esters may be used such as methyl, benzyl or aryl in a range of alcoholic solvents such as propanol or butanol.

Intermediate XV may be converted to XVI according to methods already described in reaction scheme 1.

Reduction of both esters in XVI to give I-n may be accomplished according to the preparation of la from Xl (see Reaction Scheme 1), preferably with lithium aluminium hydride in ether.

Using basic hydrolysis, the 2-position ester may be selectively cleaved to give carboxylic acid XVII. Any strong mineral base is suitable for this purpose, preferably hydroxide ions (sodium or potassium hydroxide), in an alcoholic solvent such as ethanol, propanol, butanol.

XVII may then be derivatised with N, O-dimethyl hydroxylamine according to intermediate III (see Reaction Scheme 1) to give the amide XVIII. Reduction of this amide and the ester in XVIII with lithium aluminium hydride (as above for the synthesis of I-n) gives aldehyde I-o. Grignard addition to the aldehyde in I-o gives compounds I-p, using the same method as for the synthesis of I-c (reaction scheme 1).

Reaction scheme 7: p H according to, R C02 Et reaction scheme 1 1 CIH. H2N"") r + I I > 3 R2.,'S O v C02Et R V CO, Et R)-- XIX XX XXI 1° , R' c N NU R'L/OH OH RS + HO I-q wherein Rl, R2 and R3 are as defined for compounds of formula I.

Preparation of intermediate XX may be constructed using a cycloaddition reaction according to the method of Yavari, Synthetic Communications, 1996,4495-4500 (Scheme 2a), as for intermediate XV.

Reduction of the ester and ketone in XXI to give I-q may be accomplished with lithium aluminium hydride in ether, as for I-p and I-a.

Reaction scheme 8: 1 1 R R R Rz. S NI Rs y R2. S N Rs y 2. S N Rs Fi N 5 s N OtBu R3 H R3 N'/OMe 0 0 0 \- O XI-a XXII I-s MeO accordingto reaction scheme 1 R1 R' Fut R R S N R 5 I-r 0 , R'R3 R3) NH2 Ss tNX R5 I-r I-t o R' R Ru O 0 to R3 N o I-s'R' (i. e. R4 = CONR'R") RZ, S \/R R I-u N 1-u

wherein Rl, R2, R3'and R5 are as defined for compounds of formula I.

Tert.-butyl ester XI-a (prepared according to reaction scheme 1) may be hydrolysed using methods known in the art, such as trifluoroacetic acid in dichloromethane, to give the carboxylic acid XXII, a versatile intermediate which may be either thermally decarboxylated to I-r or derivatised further to amide I-s. Similar amide bond formations of XXII may be carried out with a variety of amines to give amides I-s'where, R'and R"are defined above. Treatment of I-s with trifluoroacetic acid in dichloromethane reveals the primary amide 1-t. Dehydration of I-t to give 1-u may be achieved with Lawessons reagent according to Cava, Michael P.; Levinson, Matthew I Tetrahedron (1985), 41 (22), 5061-87, which gives the nitrile Reaction scheme 9: R R1 1 i R p 1 1 R R R R3 fixture i-r(R5 = methyl) I-v 1-w (according to reaction scheme 8) R R 1 1 R \N/OH t R2'S \N/\ b _'. 2 R I-z R3I x separated R I-y

wherein Rl, R2 and R3 are as defined for compounds of formula I.

In reaction scheme 9, compound I-r (R = methyl, synthesized according to reaction scheme 8), may be oxidised with lead tetraacetate to give a mixture of the aldehyde I-v and acetate I-w. Lead tetraacetate is a well known oxidant to those skilled in the art but other oxidants, such as potassium permanganate may also be used to oxidise aromatic methyl groups as in I-r.

Acetate 1-w (crude) may then be hydrolysed to primary alcohol I-x using any method known in the art, such as alkaline hydrolysis with sodium or potassium hydroxide.

On purification the by-product I-y was isolated. Alcohol I-x may then be derivatised to the primary carbamate I-z using trichloroacetyl isocyanate. The starting alcohol may be conveniently dissolved in a suitable organic solvent such as dichloromethane or chloroform and the reagent trichloroacetyl isocyanate added keeping the reaction temperature below 5 degrees but above-10 degrees. The work up involves use of bases such as sodium or potassium carbonate followed by purification using standard procedures. Other methods known in the art are not effective in this transformation, such as chlorosulfonyl isocyanate or trimethylsilyl isocyanate.

Reaction scheme 10:

wherein Rl, R3 and R5 are as defined for compounds of formula I, A is Cl-4-alkoxy or amino and R is Cl 4-alkyl.

In reaction scheme 10, intermediate XXIII (synthesized according to reaction scheme 1 using 3-bromo-5-chlorophenyldisulfide) may be transformed to I-aa using sp2-sp2 coupling reactions known to persons skilled in the art (e. g. from J. March (1992), "Advanced Organic Chemistry: Reactions, Mechanisms, and Structure", 4 ed. John Wiley & Sons). Such reactions are typically catalysed by a suitable palladium species such as tetrakis (triphenylphosphine) palladium, palladium acetate or dibenylideneacetone palladium. Nitrile groups may be installed using the reactivity of the aryl bromide XXIII using copper (I) cyanide to give I-ab. This reaction may also be performed on the aryl dibromide to give the aryl dinitrile.

Reaction scheme 11:

wherein R', R3 and R5 are as defined for compounds of formula I and n is 0 or 1.

In reaction scheme 11, intermediate XXIV, a subset of XXIII, may be reduced to the saturated alkyl chain I-ac by palladium catalysed hydrogenation. Oxidation of XXIV via osmium catalysed dihydroxylation gives I-ae. Sodium periodate cleavage of I-ae gives alcohol I-ad, according to standard procedures well known in the art.

The following assay methods are described.

HIV-1 reverse transcriptase assay : Inhibitor ICON determination.

HIV-1 RT assay was carried out in 96-well Millipore filtermat NOB50 plates using purified recombinant enzyme and a poly (rA)/oligo (dT) 16 template-primer in a total volume of 50 pL. The assay constituents were 50 mM Tris/HCl, 50 mM NaCI, 1 mM EDTA, 6 mM MgCl2, 5 uM dTTP, 0.1 Ci [H] dTTP, 5 jg/ml poly (rA) pre annealed to 2.5 µg/ml oligo (dT) 16 and a range of inhibitor concentrations in a final concentration of 10% DMSO. Reactions were initiated by adding 5 nM HIV-1 RT and after incubation at 37°C for 30 min, they were stopped by the addition of 50 p1 ice cold 20% TCA and allowed to precipitate at 4°C for 30 min. The precipitates were collected by applying vacuum to the plate and sequentially washing with 2 x 200 pl of 10% TCA and 2 x 200 ul 70% ethanol.

Finally the plates were dried and radioactivity counted in a Wallac Microbeta 1450 after the addition of 15 ul scintillation fluid per well. Iso s were calculated by plotting % inhibition versus logic inhibitor concentrations.

Antiviral assay method Anti-HIV antiviral activity was assessed using an adaptation of the method of Pauwels et al. {Pauwels et al., 1988, J Virol Methods 20: 309-321}. The method is based on the ability of compounds to protect HIV-infected T lymphoblastoid cells (MT4 cells) from cell-death mediated by the infection. The endpoint of the assay was calculated as the concentration of compound at which the cell viability of the culture was preserved by 50% ('50% inhibitory concentration', IC50). The cell viability of a culture was determined by the uptake of soluble, yellow 3- [4, 5-dimethylthiazol-2-yl]-2, 5-diphenyltetrazolium bromide (MTT) and its reduction to a purple insoluble formazan salt. After solubilization, spectrophotometric methods were employed to measure the amount of formazan product.

MT4 cells were prepared to be in logarithmic-phase growth and a total of 2 x 106 cells infected with the HXB2-strain of HIV at a multiplicity of 0.0001 infectious units of virus per cell in a total volume of between 200-500 microlitres. The cells were incubated with virus for one h at 37°C before removal of virus. The cells are then washed in 0.01 M phosphate buffered saline, pH 7.2 before being resuspensed in culture medium for incubation in culture with serial dilutions of test compound. The culture medium used was RPMI 1640 without phenol red, supplemented with penicillin, streptomycin, L- glutamine and 10% fetal calf serum (GM10).

Test compounds were prepared as 2 mM solutions in dimethyl sulphoxide (DMSO).

Four replicate, serial 2-fold dilutions in GM10 were then prepared and 50 microlitres amounts placed in 96-well plates over a final nanomolar concentration range of 625-1.22.

Fifty microlitres GM10 and 3.5 x 104 infected cells were then added to each well. Control cultures containing no cells (blank), uninfected cells (100% viability; 4 replicates) and infected cells without compound (total virus-mediated cell death; 4 replicates) were also prepared. The cultures were then incubated at 37 °C in a humidified atmosphere of 5% CO2 in air for 5 d.

A fresh solution of 5 mg/mL MTT was prepared in 0.01 M phosphate buffered saline, pH 7.2 and 20 microlitres added to each culture. The cultures were further incubated as before for 2 h. They were then mixed by pipetting up and down and 170 microlitres of Triton X-100 in acidified isopropanol (10% v/v Triton X-100 in 1: 250 mixture of concentrated HCl in isopropanol). When the formazan deposit was fully solubilized by further mixing, the absorbance (OD) of the cultures was measured at 540nm and 690nm wavelength (690nm readings were used as blanks for artefacts between wells). The percent protection for each treated culture can be calculated from the equation: % Protection = (OD drug-treated cultures)- (OD untreated virus control cultures) x 100% (OD uninfected cultures)- (OD untreated virus control cultures) In the assay, compounds of the formulas I range in activity from an IC50 of about 0.5 to about 5000 nM, with preferred compounds having a range of activity from about 0.5 to about 750 nM, more preferably about 0.5 to 300 nM, and most preferably about 0.5 to 50 nM. Structure RT ICso/nM HIV ICs0/nM ci N CI ./I s \N/79 17.5 du08 CI CI s N 930 580 OH CI N^5 \ s N 4120 ND ho zu \ X OH 260 11.5 OH ZU F /I s N 5430 ND OH : : K cl u s N 86 69 oh cri N cl cl--q 5 N 5 493 407 Ha cri cl 1 w _I i 5 N 198 32 0 cul ci ci s 117 44 cl CL N 91 16 N=N'--N- cl N \ ere0 90 \ zu cl Ci fN CI X °\ 658 91 S \ cri -A 289 183 OH ci c cl-qc, 972 ND a N xi 5 N s 2450 ND N CI CRI 1/ i 5 287 49 OH cri C) 150 22 NH O ci ci 125 94 ci oh / 283 84 0 \/ \ u N ci nez t ° NH2 33 16 Z CL CRI roll WH 43 11 OH ciS HS 272 110 OH CRI CI 60 10 OH -.-OH ND = not determined

It will be understood that references herein to treatment extend to prophylaxis as well as to treatment of existing conditions. It will also be understood that references to the treatment of animals includes the treatment of humans as well as other mammals.

In the present specification"comprise"means"includes or consists of'and "comprising"means"including or consisting of'.

The features disclosed in the foregoing description, or the following claims, or the accompanying drawings, expressed in their specific forms or in terms of a means for performing the disclosed function, or a method or process for attaining the disclosed result, as appropriate, may, separately, or in any combination of such features, be utilised for realising the invention in diverse forms thereof.

The pyrrole derivatives provided by the present invention can be used together with a therapeutically inert carrier as medicaments in the form of pharmaceutical preparations.

The pharmaceutical preparations can be administered enterally, such as orally, in the form of tablets, coated tablets, dragees, hard and soft gelatine capsules, solutions, emulsions or suspensions, or nasally, e. g. in the form of nasal sprays. They can also be administered rectally, e. g. in the form of suppositories, or parenterally, (e. g. intramuscularly, intravenously, or subcutaneously), for example, in the form of injection solutions.

For the manufacture of pharmaceutical preparations the pyrrole derivatives can be formulated with therapeutically inert, inorganic or organic carriers.

Lactose, corn starch or derivatives thereof, talc, stearic acid or its salts can be used, for example, as such carriers for tablets, coated tablets, dragees and hard gelatine capsules.

Suitable carriers for soft gelatine capsules are, for example, vegetable oils, waxes, fats, semi-solid and liquid polyols and the like.

Suitable carriers for the manufacture of injection solutions are, for example, water, saline, alcohols, polyols, glycerine, vegetable oils and the like. Natural or hardened oils, waxes, fats, semi-liquid or liquid polyols and the like are suitable carriers for the manufacture of suppositories. The pharmaceutical preparations of the present invention may also be provided as sustained release formulations or other appropriate formulations.

The pharmaceutical preparations can also contain preservatives, solubilizers, stabilizers, wetting agents, emulsifiers, sweeteners, colorants, flavourants, salts for adjustment of the osmotic pressure, buffers, masking agents or antioxidants.

The pharmaceutical preparations may also contain other therapeutically active agents such as those mentioned above.

The pyrrole derivatives provided by the invention in the treatment of an immune mediated condition or disease, a viral disease, a bacterial disease, a parasitic disease, an inflammatory disease, a hyperproliferative vascular disease, a tumor, or cancer.

The dosage can vary within wide limits and will, of course, be adjusted to the individual requirements in each particular case.

Dosage levels of between about 0.01 and about 100 mg/kg body weight per day in monotherapy and/or in combination therapy are commonly administered from about 1 to 5 times per day. A typical preparation will contain from about 5% to 95% active compound (w/w). The daily dosage can be administered as a single dosage or in divided dosages.

The pyrrole derivatives provided by the present invention or the medicaments thereof may be for use in monotherapy and/or combination therapy, i. e. the treatment may be in conjunction with the administration of one or more additional therapeutically active substance (s). When the treatment is combination therapy, such administration may be concurrent or sequential with respect to that of the pyrrole derivatives of the present invention. Thus, concurrent administration, as used herein, includes administration of the agents in conjunction or combination, together, or before or after each other.

It will be understood that references herein to treatment extend to prophylaxis as well as to treatment of existing conditions. Treatment of a disease or condition, as used herein, also includes preventing, inhibiting, regressing, reversing, alleviating or relieving the disease or condition, or the clinical symptoms thereof. The term"subject"as used herein refers to animals, including humans and other mammals.

With regard to the starting materials that are known compounds some of these may be purchased from commercial suppliers. Other starting materials that are known and their analogues can be prepared by methods well known in the art. Examples of compounds available from commercial suppliers, and citations to the synthesis of other compounds and their analogues are provided in the following: The described NMR spectra were recorded on a Bruker DRX 400 MHz spectrometer with the probe temperature set at 300 K.

The mass spectra indicated by" (M+ ; EI)", were recorded under electron impact conditions (EI), on a THERMOQUEST MAT95 S with a source temperature of 200°C.

Other mass spectra were recorded under electrospray ionization spectra (ESI) conditions, on one of the following machines: a) THERMOQUEST SSQ 7000 [Solvent 0.085% TFA in 90% Acetonitrile/water ; flow rate 100 microliters/minute; capillary 250°C ; spray voltage 5KV ; sheath gas 80 psi], or b) LC-MS system (liquid chromatograph coupled to mass spectrum) THERMOQUEST TSQ 7000 ELECTROSPRAY or MICROMASS PLATFORM ELECTROSPRAY [Solvent 0.1% TFA in water or 0.085% TFA in 90% acetonitrile/water or 0.085% TFA in acetonitrile].

In the following examples the abbreviations used have the following significations: min minute (s) h hour (s) d day (s) EDAC l-Ethyl-3- (3-dimethylaminopropyl)-carbodiimide hydrochloride HOBt 1-Hydroxybenzotriazole The following examples illustrate the present invention: Example 1 5-(3-5-Dichlorophenylthio)-4-isopropyl-2-methyl-1-[(4-pyridy l)methyl]-1H-pyrrole-3- methanol A solution containing O. lg of ethyl 5- (3, 5-dichlorophenylsulphanyl)-4-isopropyl-2- methyl-1-pyridin-4-yl-lH-pyrrole-3-carboxylate in 0.5 ml of anhydrous diethyl ether was added dropwise to 0.54 ml of a 1M solution of lithium aluminium hydride which was stirred and cooled at 0-5°C. The mixture was stirred at 5°C for 1 h then at room temperature for 1 h. The mixture was cooled again to 5°C and quenched with saturated ammonium chloride solution, then extracted three times with 10ml of ethyl acetate. The combined extracts were washed with 10ml of brine, then dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using methanol/dichloromethane (1 : 19) for the elution to give 70mg of 5- (3, 5- dichlorophenylthio)-4-isopropyl-2-methyl-1- [ (4-pyridyl) methyl]-lH-pyrrole-3-methanol as a pale orange gum. Mass spectrum (ESI) m/z 421 [M+H] +. tH SMR (CDCl3) 1.31 (d, 6H), 2.21 (s, 3H), 3.24 (m, 1H), 4.66 (s, 2H), 5.10 (s, 2H), 6.68 (d, 2H), 6.74 (m, 2H), 6.98 (t, 1H), 8.44 (m, 2H).

The starting material ethyl 5- (3, 5-dichlorophenylsulphanyl)-4-isopropyl-2-methyl- 1-pyridin-4-yl-lH-pyrrole-3-carboxylate was prepared as follows:

(A) A solution containing 18.8g of N-tert.-butoxycarbonylglycine in 180ml of anhydrous dichloromethane was stirred under nitrogen and cooled at 0-5°C while 11.5g of N, O-dimethylhydroxylamine hydrochloride, 27.1g of N-ethylmorpholine and 22.5g of N- ethyl-N'- (3-dimethylaminopropyl) carbodiimide hydrochloride were added. The mixture was allowed to warm slowly to room temperature and stirred for 16 h. The mixture was washed twice with 150ml of 1M hydrochloric acid, and 150ml of saturated sodium hydrogen carbonate then dried over anhydrous sodium sulphate, filtered and evaporated to give 22.5g of N-tert.-butoxycarbonylglycine N-methyl-N-methoxyamide as a white solid which was used without further purification.

(B) A solution of 10. 9g of N-tert.-butoxycarbonylglycine N-methyl-N- methoxyamide in 300ml of anhydrous tetrahydrofuran and 100ml of anhydrous diethyl ether was cooled at 0-5°C while 100ml of a 2M solution of isopropyl magnesium chloride in tetrahydrofuran was added slowly. The mixture was stirred at 0-5°C for 4 h then poured into 1.5 litre of 1M hydrochloric acid. The product was extracted with three portions of 500ml diethyl ether. Combined extracts were washed with 500ml brine then dried over anhydrous magnesium sulphate, filtered and evaporated to give 8.38g of 4-tert.- butoxycarbonylamino-2-methyl-3-butanone as a colourless oil which was used without further purification.

(C) 7.03g of 4-tert.-butoxycarbonylamino-2-methyl-3-butanone was added to 80ml of an ice cold 4M solution of hydrogen chloride in ethyl acetate. The solution was stirred at 0-5°C for 1 h during which time a precipitate separated. The mixture was evaporated under reduced pressure and the residue triturated with anhydrous ether. The white solid product was filtered off, washed with anhydrous diethyl ether and dried to give 4.14g of 4-amino-2-methyl-3-butanone hydrochloride.

(D) A solution containing 0.32g of 4-amino-2-methyl-3-butanone hydrochloride, 0.33g of ethyl acetoacetate and 0.28g of sodium acetate in 2ml of 75% acetic acid was heated at 100°C for 1.5 h. The mixture was poured into 10ml of water and extracted three times with 10ml of diethyl ether. Combined extracts were washed three times with 10ml of saturated sodium hydrogen carbonate and with 10ml of brine then dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using dichloromethane for the elution to give 0.15g of ethyl 4-isopropyl-2-methyl-lH-pyrrole-3-carboxylate. Recrystallisation from isohexane gave analytically pure material of melting point 67-68.5°C; mass spectrum (EI) m/z 195 [M] +.

(E) A solution of 1.03g of ethyl 4-isopropyl-2-methyl-lH-pyrrole-3-carboxylate in 27ml of anhydrous dichloromethane was treated with 2.06g of N-iodosuccinimide and stirred at room temperature for 2 h. The mixture was diluted with a further 50ml of

dichloromethane and washed with 50ml of saturated sodium thiosulphate solution and 50ml of saturated sodium hydrogen carbonate solution. The dichloromethane extract was dried over anhydrous sodium sulphate then filtered and evaporated. The residue was triturated with 50ml of petroleum ether (bp 40-60°C). The orange solid product was filtered off and dried to give 1.32g of ethyl 5-iodo-4-isopropyl-2-methyl-lH-pyrrole-3- carboxylate; mass spectrum (ESI) m/z 322 [M+H] +.

(F) A solution of 1.3g of ethyl 5-iodo-4-isopropyl-2-methyl-lH-pyrrole-3- carboxylate in 8ml of anhydrous dimethyl sulphoxide was stirred under nitrogen at room temperature and 39mg of lithium hydride added followed after 10min by 0.86g of bis- (3, 5- dichlorophenyl) disulphide. The mixture was stirred under nitrogen and heated at 60°C for 6 h then stood at room temperature for 16 h. The mixture was diluted with 150ml of water and extracted three times with 75ml of diethyl ether. Combined extracts were washed with 50ml of brine then dried over anhydrous magnesium sulphate, filtered and evaporated to give a brown gum which crystallised. Recrystallisation from methylcyclohexane gave 0.66g of ethyl 5- (3, 5-dichlorophenylsulphanyl)-4-isopropyl-2-methyl-lH-pyrrole-3 -carboxylate of melting point 148-151°C ; mass spectrum (EI) m/z 371 [M] +.

(G) A solution of O. lg of ethyl 5- (3, 5-dichlorophenylsulphanyl)-4-isopropyl-2- methyl-lH-pyrrole-3-carboxylate in 2ml of anhydrous tetrahydrofuran was stirred at room temperature under nitrogen and treated with 65mg of 4-bromomethylpyridine hydrobromide, 5mg of tetra-n-butylammonium bromide and 24mg of powdered sodium hydroxide. The mixture was stirred at room temperature for 20 h then diluted with 20ml of water and extracted three times with 10ml of ethyl acetate. Combined extracts were washed with 10ml of brine, then dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using ethyl acetate/isohexane (1: 1) for the elution to give 0.104g of ethyl 5- (3, 5- dichlorophenylsulphanyl)-4-isopropyl-2-methyl-1-pyridin-4-yl -1H-pyrrole-3-carboxylate as a colourless gum. Mass spectrum (ESI) m/z 463 [M+H] +. lu NMR (CDC13) 1.32 (d, 6H), 1.40 (t, 3H), 2.45 (s, 3H), 3.61 (m, 1H), 4.34 (q, 2H), 5.16 (s, 2H), 6.69 (d, 2H), 6.76 (m, 2H), 7.01 (t, 1H), 8.47 (m, 2H).

Example 2 <BR> <BR> <BR> <BR> <BR> <BR> 5-(3*5-Dichlorophenylthio)-4-isopropyl-2-methyl-1- [ (4-pyridyl) methyll-lH-pyrrole-3- carboxaldehyde A solution of 0. 2g of 3, 5-dichlorophenylsulphanyl-3-hydroxymethyl-4-isopropyl-2- methyl-l-pyridin-4-yl-pyrrole and 7.5mg of 2, 2,6,6-tetramethylpiperidine N-oxide in

0.5ml of anhydrous dichloromethane was treated with 0.17g of iodobenzene diacetate. The mixture was stirred at room temperature for 4 h then diluted with 10 rnl of dichloromethane and washed with 10ml of saturated sodium thiosulphate and 10ml of saturated sodium hydrogen carbonate, then dried over anhydrous sodium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using methanol/dichloromethane (1: 49) for the elution to give 50mg of 5- (3, 5- dichlorophenylthio)-4-isopropyl-2-methyl-1- [ (4-pyridyl) methyl]-lH-pyrrole-3- carboxaldehyde as a gum. Mass spectrum (ESI) m/z 419 [M+H] +. 1H NMR (CDCl3) 1.36 (d, 6H), 2.53 (s, 3H), 3.46 (m, 1H), 5.16 (s, 2H), 6.69 (d, 2H), 6.74 (m, 2H), 7.02 (t, 1H), 8.47 (m, 2H), 10.21 (s, 1H).

Example 3 <BR> <BR> <BR> <BR> <BR> 5-(3. 5-Dichlorophenylthio)-4-isopropyl-alpha (RS)-methyl-1- [(4-pyridvl) methyll-1H-<BR> <BR> <BR> <BR> pyrrole-3-ethanol A solution of 90mg of 5- (3, 5-dichlorophenylsulphanyl)-4-isopropyl-2-methyl-1- pyridin-4-yl-lH-pyrrole-3-carboxaldehyde in lml of anhydrous tetrahydrofuran was stirred under nitrogen and cooled at 0-5°C while 0.21ml of a 1.4M solution of methyl magnesium bromide in toluene/tetrahydrofuran (75: 25) was added dropwise. The mixture was stirred at 0-5°C for 2 h then diluted with 10ml of saturated ammonium chloride solution and extracted twice with 10ml of ethyl acetate. Combined extracts were washed with 10ml of brine, dried over anhydrous magnesium sulphate, filtered and evaporated.

The residue was purified by flash chromatography on silica gel using methanol/dichloromethane (1: 19) for the elution to give 19mg of 5- (3, 5- dichlorophenylthio)-4-isopropyl-alpha (RS)-methyl-1- [(4-pyridyl) methyl]-lH-pyrrole-3- ethanol as a gum. Mass spectrum (ESI) m/z 435 [M+H] +. lH NMR (CDC13) 1.26 (d, 3H), 1.29 (d, 3H), 1.55 (d, 3H), 1.77 (bs, 1H), 2.30 (s, 3H), 3.30 (m, 1H), 5.08 (s, 2H), 5.25 (q, 1H), 6.67 (d, 2H), 6.71 (m, 2H), 6.97 (t, 1H), 8.43 (m, 2H).

Examples 4-9 In a manner analogous to that described in example 1-3, starting with N-tert.- butoxycarbonylglycine (commercially available from Fluka or Aldrich), the compounds shown in table 2 were also prepared: Table 2 Example Structure Name Mass Spectrum (m/z ES, +ve ion) 4 cl 5_35_ cl Dichlorophenylthio)- N 4-isopropyl-1, 2- 344 < dimethyl-lH-pyrrole- OH 3-methanol 5 cl 5- (3, 5- ci Dichlorophenylthio)- 1-ethyl-4-isopropyl-2-356 methyl-lH-pyrrole-3- methanol 6 1-Benzyl-5- (3, 5- dichlorophenylthio)-4- isopropyl-2-methyl- 1H-pyrrole-3-420 methanol 1_ (Cyclohexylmethyl)- cl 5- (3, 5- dichlorophenylthio)-4- isopropyl-2-methyl- OH 1H-pyrrole-3- methanol 5_ (35_ cl Dichlorophenylthio)- N 4-isopropyl-2-methyl- 421 1- (2-pyridyl) methyl]- 1H-pyrrole-3- methanol

9 ci ci N 1 5- (3, 5- c- Dichlorophenylthio)- N 4-isopropyl-2-methyl- s 421 M [ (3-pyridyl) methyl]- OH 1H-pyrrole-3- methanol Examples 10-15 In a manner analogous to that described in example 1-3, starting with N-tert.- butoxycarbonylglycine (prepared as described in example Ia), the compounds shown in table 3 were also prepared: Table 3 Example Structure Name Mass Spectrum (m/z ES, +ve ion) 10 4-Isopropyl-2-methyl-5- phenylthio-l- [ (4- pyridyl) methyl]-1H- 352 pyrrole-3-methanol OH 5- (3-Chlorophenylthio)- cl 4-isopropyl-2-methyl-l- [ (4-pyridyl) methyl]-IH- 387 pyrrole-3-methanol OH 12 o N N 4-Isopropyl-2-methyl-5- (3-nitrophenylthio)-1- \5 N 1 (4-pyridyl) methyl]-1H- pyrrole-3-methanol ß OH OH 13 Dimethylphenylthio)-4- isopropyl-2-methyl-l-380 [ (4-pyridyl) methyl]-1H- OH pyrrole-3-methanol 4-Isopropyl-5- isopropylthio-2-methyl- Nl- [ (4-pyridyl) methyl]- < lH-pyrrole-3-methanol > OH OH 15 4-Isopropyl-2-methyl-5- methylthio-1- [ (4- N pyridyl) methyl]-1H- pyrrole-3-methanol > OH OH

Examples 16-20 In a manner analogous to that described in example 1-3, starting with N-tert.- butoxycarbonylglycine (prepared as described in example Ia), the compounds shown in table 4 were also prepared: Table 4 Example Structure Name Mass Spectrum (m/z ES, +ve ion) 0 CI. Dichlorophenylthio)-2- N methyl-4-phenyl-1- [ (4- pyridyl) methyl]-1H- 455 OH pyrrole-3-methanol 4- (4-Chlorophenyl)-5- cl 9) (3, 5-dichlorophenylthio)- N 2-methyl-1- [ (4- pyridyl) methyl]-lH- 490 OH pyrrole-3-methanol cl 18 ci N 5- (3, 5- cl Dichlorophenylthio)-2- methyl-4- (4- methylphenyl)-1- [ (4-469 /= (OH pyridyl) methyl]-lH- pyrrole-3-methanol 19 ci 5- (3, 5- ct Dichlorophenylthio)-4- S N (4-methoxyphenyl)-2- methyl-1- [ (4-485 OH pyridyl) methyl]-lH- pyrrole-3-methanol _ 20 Cl 8 er 4-(3, 4-Dichlorophenyl)- c 5- (3, 5- dichlorophenylthio)-2- methyl-l- [ (4- 524 OH pyridyl) methyl]-lH- pyrrole-3-methanol cl ci

Examples 21-22 In a manner analogous to that described in example 1-3, starting with N-tert.- butoxycarbonylglycine (prepared as described in example Ia) transferred to a compound of the formula XI, the compounds shown in table 5 were also prepared via hydrolysis of XI when R = tert.-butyl (example 21) or via intermediate XII (Scheme 3) where R5a _ amino (example22): Table 5 Example Structure Name Mass Spectrum (m/z ES, +ve ion) 21 cl cl Dichlorophenylthio)-4- N isopropyl-2-methyl-1- [ (4- 435 pyridyl) methyl]-1H- pyrrole-3-carboxylic acid 22 ci 5- (3, 5- Dichlorophenylthio)-4- isopropyl-2-methyl-l- [ (4- 434 pyridyl) methyl]-1H- NH2 pyrrole-3-carboxamide ru

Examples 23 In a manner analogous to that described in example 1-3, starting with N-tert.- butoxycarbonylglycine (prepared as described in example Ia) transferred to a compound of the formula Ic, the compounds shown in table 6 were prepared by mesylation reaction with for example CH3SO2C1 and Et3N followed by a reduction reaction with for example Zn/acetic acid (as described in J. Org. Chem. 1997,62,9223): Table 6 Example Structure Name Mass Spectrum (m/z ES, +ve ion) 23-C _ __-. cl 'jv Dichlorophenylthio)-3- isopropyl-4, 5-dimethyl- 405 1H-pyrrol-l- ß yl] methyl] pyridine

Examples 24-25 In a manner analogous to that described in example 1-3, starting with N-tert.- butoxycarbonylglycine (prepared as described in example Ia) the compounds shown in table 7 were prepared from la by conversion of alcohol to chloride then displacement of chloride with azide and finally reduction of azide with hydrogen (example 24) or via nucleophilic substitution reaction with a methoxide anion (example 25) of the chloride of the alcohol of the formula Ia.

Table 7 Example Structure Name Mass Spectrum (m/z ES, +ve ion) 24 ci 5- (3, 5- Dichlorophenylthio)- N N 4-isopropyl-2-methyl- 420 1- [ (4-pyridyl) methyl]- ß NHz lH-pyrrole-3- methylamine . ll r cl 9 e) Dichlorophenylthio)- 5 N 3-isopropyl-4- 5 N 435 (methoxymethyl)-5- ß \ methyl-lH-pyrrol-l- yl] methyl] pyridine

Examples 26-28 In a manner analogous to that described in example 1-3, starting with N-tert.- butoxycarbonylglycine (prepared as described in example Ia) the compounds shown in table 8 were also prepared up to intermediate V which was then taken forward via Reaction Scheme 6. Example 28 was prepared according to Scheme 1 where R = ethyl in intermediate VI.

Table8 Example Structure Name Mass Spectrum (m/z ES, +ve ion) 26 cI cl 5_ (3,5- Dichlorophenylthio)-3- t rDicMorophenylthio)-3- (hydroxymethyl)-4- isopropyl-l- [ (4- H pyridyl) methyl]-lH- pyrrole-2-methanol 27 5- (3, 5- Dichlorophenylthio)-4- isopropyl-1- [ (4- pyridyl) methyl]-lH- OH pyrrole-3-methanol 28 c \ CI, 9 e) Dichlorophenylthio)-2- 5 N ethyl-4-isopropyl-1- [(4-435 pyridyl) methyl]-1H- pyrrole-3-methanol

Examples 29-30 In a manner analogous to that described in example 1-3, starting with N-tert.- butoxycarbonylglycine (prepared as described in example Ia) the compounds shown in table 9 were also prepared. The examples are prepared by bromination of the compounds of the formula VII to the corresponding 2-substituted bromopyrrole which is then further reacted with the corresponding neutral oxygen nucleophile in the presence of Et3N to obtain the corresponding oxy pyrrole derivative (example 29). To obtain the corresponding N-substituted pyrrole derivatives (example 30), the above-mentioned 2- substituted bromopyrrole is reacted with a primary or a secondary amine.

Table 9 Example Structure Name Mass Spectrum (m/z ES, +ve ion) 29 ci 5- (3, 5-Dichlorophenoxy)- ci 4-isopropyl-2-methyl-1- o N [(4-pyridyl) methyl]-lH- pyrrole-3-methanol OH y \-oH 30-ct ~ 5-[(3, 5- Dichlorophenyl) methylami N N no]-4-isopropyl-2-methyl- Q 1-[(4-pyridyl) methyll-lH- pyrrole-3-methanol

Examples 31-32 In a manner analogous to that described in example 1-3, starting with N-tert.- butoxycarbonylglycine (prepared as described in example Ia) the compounds shown in table 10 were also prepared. The examples are prepared by coupling reaction of the corresponding compounds of the formula 5a with the corresponding ß-keto ester of the formula VI to obtain examples 31-32.

Table 10 Example Structure Name Mass Spectrum (m/z ES, +ve ion) 31 i N 5-Benzyl-4-isopropyl-2- methyl-1- [ (4- pyridyl) methyl]-lH- 334 pyrrole-3-methanol OH 4-Isopropyl-2-methyl- 1, 5-bis [ (4- pyridyl) methyl]-1H- pyrrole-3-methanol OH

Examples 33-35 In a manner analogous to that described in example 1-3, starting with N-tert.- butoxycarbonylglycine (prepared as described in example Ic) example 34 was made according to reaction scheme 9.

Table 11 Example Structure Name Mass Spectrum (m/z ES, +ve ion) 33 5- (3,5- cl 9 Y Dichlorophenylthio)-l- N isopropyl-3-methyl-4- N OH [ (4-pyridyl) methyl]-lH- pyrrole-2-methanol 34 ,"5_ (3, 5- cl V Dichlorophenylthio)-4- S N isopropyl-l- [(4-407 mOH pyridyl) methyl]-1H- pyrrole-2-methanol 35 5- (3, 5- Dichlorophenylthio)-4- isopropyl-3-methyl-1- [ (4-pyridyl) methyll-lH- pyrrole-2-methanol Example 93 Ex. STRUCTURE SYSTEMATIC NAME MS Cl eN 4- [ [3-(Azidomethyl)-5-(3, 5- ci I dichlorophenylthio)-4-isopropyl-2- 93 As_6) methyl-1-pyrrolyl] methyl] pyridine 446 N=N=N

To a solution of 200mg of 4- [ [3- (Chloromethyl)-5- (3, 5-dichlorophenylthio)-4- isopropyl-2-methyl-l-pyrrolyl] methyl] pyridine in 5mL of DMF was added 137mg of sodium azide. The mixture was stirred at room temperature for 18 h. The yellow solution was quenched with saturated sodium bicarbonate solution and extracted with diethyl ether. The combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 2) then ethyl acetate for the elution to give 129mg as a yellow oil. Mass spectrum (ESI) m/z 446 [M+H] +. Mass spectrum (ESI) m/z 446 [M+H] +.

Example 76 cl cri \ Dichlorophenylthio)-4-525 N \N isopropyl-2-methyl-1- [ (4- P PY Y-t- pyridyl) methyll-lH-pyrrol-3- yl] methyll-4-pyrldineacetamide To a solution of 70mg of 5- (3, 5-Dichlorophenylthio)-4-isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-lH-pyrrole-3-methylaminein 3mL of dichloromethane was added 30mg of isonicotinyl chloride and 50mg of triethylamine. The mixture was stirred at room temperature for 18 h then quenched with saturated sodium bicarbonate solution and extracted with dichloromethane. The combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was preabsorbed onto silica then purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 9 then 1: 4) for the elution to give 50mg as a cream solid. Mass spectrum (ESI) m/z 525 [M+H] +.

The starting material 5- (3, 5-Dichlorophenylthio)-4-isopropyl-2-methyl-l- [ (4- pyridyl) methyl]-lH-pyrrole-3-methylaminewas prepared as follows: To a solution of 2. 33g of 4- [ [3- (Azidomethyl)-5- (3, 5-dichlorophenylthio)-4- isopropyl-2-methyl-1-pyrrolyl] methyl] pyridinein 100mL of ethyl acetate was added 100mg of 10% Pd on carbon catalyst. The mixture was hydrogenated for 1.5 h. The mixture was filtered and evaporated to give 2.2g of a yellow oil. Mass spectrum (ESI) m/z 446 [M+H] +.

Example 95 cl, N 4- [ [2- (3, 5-Dichlorophenylthio)- cl 3-isopropyl-5-methyl-4-vinyl-1- 95 5 pyrrolyl] methyl] pyridine 417

A solution of 90mg of 5- (3, 5-dichlorophenylthio)-4-isopropyl-alpha (RS)-methyl-1- [ (4-pyridyl) methyl]-lH-pyrrole-3-ethanol in 3mL of DMSO was heated at 160°C for.

30 min. The brown solution was cooled to room temperature then quenched with saturated sodium bicarbonate solution and extracted with diethyl ether. The combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated.

The residue was purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 4 up to 1: 1) then ethyl acetate for the elution to give 28mg as a oil. Mass spectrum (ESI) m/z 417 [M+H] +.

Example 96 cl i 1 (S)- [5- (3, 5- cl Dichlorophenylthio)-4- isopropyl-2-methyl-1- [ (4- 96 9~ pyridyl) methyl]-1 H-pyrrol-3-451 OH yl]-1, 2-ethanediol OH To a degassed solution of61mg of4-t [2- (3, 5-Dichlorophenylthio)-3-isopropyl-5- methyl-4-vinyl-1-pyrrolyl] methyls pyridine in 20mL of dioxane and 3.5mL of water was added 26mg of N-methyl morpholine N-oxide and 4mg of osmium tetroxide. The reaction was kept dark by covering with aluminium foil and stirred at room temperature for 24 h.

The solution was quenched with saturated sodium bicarbonate solution and extracted with ethyl acetate. The combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated to give a brown gum which solidified on addition of ethyl acetate to give 29mg of a brown solid. This solid was further purified by HPLC to give 0.4mg of the product. Mass spectrum (ESI) m/z 451 [M+H] +.

Example 75 tcl t » [5-(3, 5-Dichloro- phenylsulfanyl)-4-isopropyl-2- 5 N methyl-1-pyridin-4-ylmethyl- 75 1H-pyrrol-3-ylj-hydroxy-acetic 493 ho acid ethyl ester

To a solution of 140mg of [5- (3, 5-Dichloro-phenylsulfanyl)-4-isopropyl-2-methyl- l-pyridin-4-ylmethyl-lH-pyrrol-3-yl]-oxo-acetic acid ethyl ester in 5mL of ethanol was added 54mg of sodium borohydride. The mixture was stirred at room temperature for 2 h. The reaction was quenched with saturated sodium bicarbonate solution and extracted with ethyl acetate. The combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 9 up to 1: 4) for the elution to give 22mg as a white foam. Mass spectrum (ESI) m/z 493 [M+H] +.

Example 107 cl/N 5- (3, 5-Dihlorophenylthio)-2- ex (hydroxymethyl)-4-isopropyl- 107 5 r-C alpha (RS)-methyl-1- [ (4- 451 pyridyl) methyl]-lH-pyrrole-3- ethanol HO To a solution of 120mg of 1- [5- (3, 5-Dichlorophenylthio)-4-isopropyl-2-methyl-1- [(4-pyridyl) methyl]-lH-pyrrol-3-yl] ethanone in 3 mL of ether at 0°C was added 1.25mL of a 1M solution of lithium aluminium hydride in ether. The reaction was allowed to warm to room temperature over 30 min. The reaction was quenched with saturated ammonium chloride solution and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over anhydrous magnesium sulphate, filtered and evaporated.

The residue was purified by flash chromatography on silica gel using ethyl acetate for the elution to give 35mg which required further purification by HPLC giving the desired product and the de-chlorinated derivative 5- (3-chlorophenylthio)-4-isopropyl-2-methyl- 1-[(4-pyridyl) methyl]-lH-pyrrole-3-(2-ethanol). Mass spectrum (ESI) m/z 451 [M+H] +.

The starting material 1- [5- (3, 5-Dichlorophenylthio)-4-isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-lH-pyrrol-3-yllethanone was prepared as follows : (A) A mixture of 2. 45g of pent-2-yn-4-one-oate ethyl ester, 3.19g of 1-amino-3- methylbutan-2-one hydrobromide and 1.44g of sodium acetate were dissolved in 88ml of ethanol and heated at reflux for 30 min. Then 8ml of concentrated hydrochloric acid were added and reflux continued. After 1 h the solvent was evaporated and the residue partitioned between saturated sodium bicarbonate solution and extracted with ethyl acetate. The combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 9 up to 1: 4) for the elution to give 750mg of 4- isopropyl-lH-pyrrole-3-ethanone-2-ethyl ester as a white foam. Mass spectrum (ESI) m/z 223 [M+H]'.

(B) Iodination, sulfuration and alkylation to give 5- (3, 5-dichlorophenylthio)-4-isopropyl- 1- [ (4-pyridyl) methyl]-lH-pyrrole-3-ethanone-2-ethyl ester were all carried out according to procedures described for examples from Scheme 1.

Example 108 cl w er 5-(3, 5-Dichlorophenylthio)-3- (hydroxymethyl)-4-isopropyl-1- 108 \ N [ (4-pyridyl) methyl]-lH-pyrrole-438 2-carboxaldehyde 0 To a solution of 88mg of 5- (3, 5-dichlorophenylthio)-4-isopropyl-3-ethyl ester-1- [ (4-pyridyl) methyl]-lH-2- [N-methyl-N-methoxyamide]-pyrrole in 5mL of THF at 0°C was added 0.33mL of a 1M solution of lithium aluminium hydride in ether. The reaction was allowed to warm to room temperature over 1 h. The reaction was quenched with saturated ammonium chloride solution and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 2) for the elution to give the desired product, 29mg of an oil, and 6mg of 5-(35-Dichlorophenylthio)-4-isopropyl-l-[(4-pyridyl) methyl]-1H-pyrrole 2,3-dicarboxaldehyde as an oil. Mass spectrum (ESI) m/z 438 [M+H] +.

The starting material 5- (3, 5-dichlorophenylthio)-4-isopropyl-3-ethyl ester-1- [ (4- pyridyl) methyl]-2- [N-methyl-N-methoxyamidel-lH-pyrrole was prepared as follows: (A) A mixture of 0. 5g of amino-3-methylbutan-2-one hydrochloride, 0.58ml of diethylacetylene dicarboxylate and 295mg of sodium acetate were refluxed in 18ml of ethanol for 10 min. A few drops of concentrated hydrochloric acid were then added and the mixture boiled further. The reaction was cooled to room temperature then partitioned between dichloromethane and ice water. The combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 9,1: 6 then 1: 4) then ethyl acetate for the elution to give 323mg of 4-isopropyl-2, 3- dicarboxylate ethyl ester as a yellow oil. Mass spectrum (ESI) m/z 253 [M+H] +.

(B) Iodination, sulfuration and alkylation to give 5- (3, 5-dichlorophenylthio)-4-isopropyl- 1- [ (4-pyridyl) methyl]-1H-pyrrole-2, 3-bisethyl ester were all carried out according to procedures described for examples from Scheme 1.

(C) To a solution of 462mg of 5- (3, 5-dichlorophenylthio)-4-isopropyl-1- [ (4- pyridyl) methyl]-lH-pyrrole-2, 3-bisethyl ester in 12mL of ethanol was added 50mg of potassium hydroxide. The mixture was refluxed for 18 h then a further 20mg of potassium hydroxide was added and refluxing continued for 3 h. The solvent was evaporated and the residue partitioned between ethyl acetate and dilute hydrochloric acid. The aqueous phase was extracted with ethyl acetate and the combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was triturated with ether to give 417mg of 5- (3, 5-dichlorophenylthio)-4- isopropyl-3-ethyl ester-1- [ (4-pyridyl) methyl]-lH-pyrrole-2-carboxylic acid as an orange foam. Mass spectrum (ESI) m/z 493 [M+H] +.

(D) To a solution of 417mg of 5- (3, 5-dichlorophenylthio)-4-isopropyl-3-ethyl ester-1- [ (4- pyridyl) methyl]-lH-pyrrole-2-carboxylic acid in lOmL of dichloromethane was added 243mg of EDAC, 171mg of HOBt, 124mg of N, N-dimethyl hydroxylamine then finally 0.33mL of N-ethyl morpholine. The reaction mixture was stirred at room temperature for 1 h. The orange solution was quenched with saturated sodium bicarbonate solution and extracted with ethyl acetate. The combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 4 then 1: 2) then ethyl acetate for the elution to give 233mg of 5- (3, 5-dichlorophenylthio)-4-isopropyl-3- ethyl ester-1- [ (4-pyridyl) methyl]- 2- [N-methyl-N-methoxyamide]-lH-pyrrole as a yellow oil. Mass spectrum (ESI) m/z 535 [M+H] +.

Example 110

5- (3, 5-Dichlorophenylthio)-3- (hydroxymethyl)-4-isopropyl- 110 \ N t alpha (RS)-methyl-l- [(4-451 pyridyl) methyl]-lH-pyrrole-2- H ethanol To a solution of 60mg of 5- (3, 5-Dichlorophenylthio)-3- (hydroxymethyl)-4- <BR> <BR> isopropyl-1- [ (4-pyridyl) methyl]-lH-pyrrole-2-carboxaldehydein ImL ofTHF was added O. lmL of a 3M solution of methyl magnesium iodide in diethyl ether. The mixture was stirred at room temperature under nitrogen for 1 h. The reaction was quenched with saturated ammonium chloride solution and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using ethyl acetate for the elution to give 22mg of a gum. Mass spectrum (ESI) m/z 451 [M+H] +.

The starting material 5- (3, 5-Dichlorophenylthio)-3- (hydroxymethyl)-4-isopropyl-l- [(4-pyridyl) methyl]-lH-pyrrole-2-carboxaldehyde was prepared as follows: To a solution of 371mg of 5- (3, 5-dichlorophenylthio)-4-isopropyl-3-ethyl ester-1- [ (4-pyridyl) methyl]- 2- [N-methyl-N-methoxyamide]-lH-pyrrole in lOmL of THF at 0°C was added 1. 4mL of a 1M solution of lithium aluminium hydride in ether. The mixture was stirred for 30 min then quenched with saturated ammonium chloride solution and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using ethyl acetate for the elution to give 223mg of 5- (3,5-dichlorophenylthio)-4-isopropyl-1- [ (4-pyridyl) methyl]-lH-pyrrole-3-methanol-2 carboxaldehyde as a gum. Mass spectrum (ESI) m/z 434 [M+H] +.

Example 111 ci ci N I 5- (3, 5-DicMorophenylthio)-4- isopropyl-1- [ (3- 111 \5 N pyridyllmethyl]-lH-pyrrole-2, 3-437 dimethanol OH

To a 1M solution of lithium aluminium hydride in ether at 0°C, under nitrogen, was added 70mg of 5- (3, 5-dichlorophenylthio)-4-isopropyl-l- [ (4-pyridyl) methyl]-1H- pyrrole-2,3-bisethyl ester as a solution in 3mL of ether. The mixture was stirred for 1 h then quenched with saturated ammonium chloride solution and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 9 then 1: 4) for the elution to give 16mg of a gum. Mass spectrum (ESI) m/z 437 [M+H] +.

Example 117 5- (3, 5-Dichlorophenylthio)-2- methyl-4-phenyl-1- [ (4- 117 s N pyridyl) methyll-lH-pyrrole-3- 469 carboxylic acid trifluoroacetate C o OH (1 : 1)

To a solution of 243mg of 5- (3, 5-dichlorophenylthio)-4-phenyl-2-methyl-1- [ (4- pyridyl) methyl]-lH-pyrrole-3-tertbutyl ester in 6ml of dichloromethane was added 6ml of trifluoroacetic acid at room temperature. The mixture was stirred for 1 h then evaporated and the residue was purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 4 then 1: 1) for the elution to give 155mg of a foam. Mass spectrum (ESI) m/z 469 [M+H] +.

Example 115 ci 5- (3,5-Dichlorophenylthio)-N- 1/f v (2,4,6-trimethoxybenzyl)-2- N 115 methyl-4-phenyl-l- [ (4- 614 o,, pyridyl) methyl]-lH-pyrrole-3- _o carboxamide 4- [ [2- (3, 5-Dichlorophenylthio)- cl 3-isopropyl-5-methyl-1- 115a N pyrrolyl] methyl] pyridine 391

To a solution of 160mg of 5-(3,5-Dichlorophenylthio)-2-methyl-4-isopropyl-1-[(4- pyridyl)methyl]-1H-pyrrole-3-carboxylic acid in 10ml of dichloromethane was added 60mg of EDAC, 40mg of HOBt, 68mg of 2, 4,6-trimethoxybenzylamine hydrochloride and 0. 1 lml of N-ethyl morpholine. The reaction mixture was stirred at room temperature for 18 h. The reaction was quenched with saturated sodium bicarbonate solution and extracted with ethyl acetate. The combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 4 then 1: 2) then ethyl acetate for the elution to give 29mg of 5- (3, 5-dichlorophenylthio)-4-isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-lH-pyrrole as an oil, mass spectrum (ESI) m/z 391 [M+H]+ and 114mg of <BR> <BR> <BR> 5-(3, 5-dichlorophenylthio)-4-isopropyl-2-methyl-1- [(4-pyridyl) methyl]-lH-pyrrole-3-N- [ (2, 4,6-trimethoxy) benzyl]-carboxamide as an oil, mass spectrum (ESI) m/z 614 [M+H] +.

Example 118

5- (3, 5-Dichlorophenylthio)-4- phenyl-2-methyl-1- [ (4- 118 s N pyridyl) methyl]-lH-pyrrole-3-468 118 AT,., 468 carboxamide w di s To a solution of 110mg of 5- (3, 5-Dichlorophenylthio)-N- (2,4,6-trimethoxybenzyl)- 2-methyl-4-phenyl-1- [ (4-pyridyl) methyl]-lH-pyrrole-3-carboxamidein 4ml of

dichloromethane was added 3ml of trifluoroacetic acid at room temperature. The mixture was stirred for 1 h then evaporated and the residue was purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 9 then 1: 4) for the elution to give 26mg of a white solid. Mass spectrum (ESI) m/z 468 [M+H] +.

Example 119 cl< er 5-(3, 5-Dichlorophenylthio)-2- methyl-4-phenyl-1- [ (4- \ N pyridyl) methyl]-lH-pyrrole-3-450 119 /,.. 450 carbonitrile 9 N

To a solution of 17mg of 5- (3, 5-Dichlorophenylthio)-4-phenyl-2-methyl-1- [ (4- pyridyl) methyl]-lH-pyrrole-3-carboxamide in toluene was added 22mg of Lawessons reagent. The mixture was refluxed for 1 h then cooled to room temperature. The reaction was quenched with saturated sodium bicarbonate solution and extracted with ethyl acetate. The combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 4 then 1: 2) then ethyl acetate for the elution to give 13mg of a gum. Mass spectrum (ESI) m/z 450 [M+H] +.

Example 113 5- (3, 5-Dichlorophenylthio)-4- Ci isopropyl-1- [ (4- 113a \5 N pyridyl) methyl]-lH-pyrrole-2-405 carbaldehyde % ci cl [5- (3, 5-Dichlorophenylthio)-4- isopropyl-1- [ (4- 113 s N (pyridyl) methyl]-1H-pyrrol-2- 447 yl] methyl acetate

To a solution of 160mg of 5-(3, 5-dichlorophenylthio)-4-isopropyl-2-methyl-1-[(4- pyridyl) methyl]-lH-pyrrole in 3ml of acetic acid was added 200mg of lead tetraacetate over 30 min. After stirring for 2 h at room temperature a further 100mg of lead tetraacetate was added and the mixture stirred for 18 h. After this time a further 100mg of lead tetraacetate was added and the mixture stirred for 18 h. The reaction was quenched with saturated sodium bicarbonate solution and extracted with ethyl acetate. The combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated.

The residue was purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 4 then 1: 2) then ethyl acetate for the elution to give 23mg of 5- (3, 5- dichlorophenylthio)-4-isopropyl-1- [ (4-pyridyl) methyl]-lH-pyrrole-2-carbaldehyde, mass spectrum (ESI) m/z 405 [M+H] +, as a brown oil and 51mg of 5- (3, 5-dichlorophenylthio)- 4-isopropyl-1-[(4-pyridyl) methyl]-lH-pyrrole-2-acylmethanol as an impure yellow foaming oil, Mass spectrum (ESI) m/z 447 [M+H] +.

Examples 112. 114 5- (3, 5-Dichlorophenylthio)-4- cI isopropyl-1- [ (4- 112 S N pyridyl) methyl]-lH-pyrrole-2-407 M methanol 4- [5- (3, 5-Dichloro- cl phenylsulfanyl)-4-isopropyl-l- 114 0 pyridin-4-ylmethyl-I H-pyrrol-445 2-yl]-but-3-en-2-one To a solution of 51mg of the impure 5- (3, 5-dichlorophenylthio)-4-isopropyl-l- [ (4- pyridyl) methyl]-lH-pyrrole-2-acylmethanol in 4ml of 50% aqueous acetone was added 50mg of powdered potassium hydroxide. The mixture was stirred at room temperature for 2 h. The reaction was quenched with water and extracted with diethyl ether. The combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated.

The residue was purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 4 then 1: 2) then ethyl acetate for the elution to give 8mg of 5- (3, 5-dichlorophenylthio)- 4-isopropyl-l- [ (4-pyridyl) methyl]-lH-pyrrole-2-methanol as a yellow gum, mass spectrum (ESI) m/z 407 [M+H] +, and 9mg of 5- (3,5-dichlorophenylthio)-4-isopropyl-l- [ (4-pyridyl) methyl]-lH-pyrrole-2- [4'-but-3-en-2-one] as a yellow gum, mass spectrum (ESI)m/z 445 [M+H] +.

Example 130

ci [5- (3, 5-Dichlorophenylthio)-4- isopropyl-1- [ (4- pyridyl) methyl]-lH-pyrrol-2- X \ ylJmethyl carbamate 0 To a solution of 103mg of 5-(3,5-Dichlorophenylthio)-4-isopropyl-1-[(4- pyridyl) methyl]-lH-pyrrole-2-methanol in 3ml of dichloromethane was added 57mg of trichloroacetyl isocyanate dropwise at 0°C. The mixture was stirred at 0°C for 2 h then evaporated. To the residue was added 2ml of methanol, lml of water and 103mg of potassium carbonate at 0°C. The mixture was warmed to room temperature and stirred for 2 h. After this time the solution was homogenous and orange in colour. The reaction was quenched with water and extracted with ethyl acetate. The combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 4) for the elution to give 27mg of a white solid. Mass spectrum (ESI) m/z 450 [M+H3+.

Example 132 ci 4- [ [2- (3-Allyl-5- chlorophenylthio)-3-isopropyl- 132/N S-methyl- [ (4- 397 pyrrolyl] methyl] pyridine -< To a solution of 80mg of 4- [ [2- (3-Bromo-5-chlorophenylthio)-3-isopropyl-5- methyl-1-pyrrolyl] methyls pyridine in 5ml of dimethoxyethane was added 156ul of allyltributyltin and 60mg of tetrakis (triphenylphosphine) palladium. The mixture was

heated to 70°C for 18 h. The mixture was directly purified by flash chromatography on silica gel using methanol/dichloromethane (1: 19) for the elution to give 40mg of a white solid. Mass spectrum (ESI) m/z 397 [M+H] +.

Example 133 ci 4- [ [2- (3-Chloro-5- I propylphenylthio)-3-isopropyl- 5-methyl-1- 133 s ß pyrrolylj methyl] pyridine 399 To a solution of 10mg of 4- [ [2- (3-Allyl-5-chlorophenylthio)-3-isopropyl-5-methyl- [ (4-pyrrolyl] methyl] pyridine in 5ml of warm ethanol was added lmg of 10% palladium on carbon. The mixture was hydrogenated for 10 min then filtered through a pad of celite.

The filtrate was evaporated to dryness to give 10mg of a white solid. Mass spectrum (ESI) m/z 399 [M+H] +.

Example 135 HO cul 5- [3-Chloro-5- r 01' (hydroxymethyl) phenylthiol-4- 135 \5 N isopropyl-2-methyl-1- [(4-430 < pyridyl) methyl]-lH-pyrrole-3- ß of 2 carboxamide To a solution of 25mg of 5- [3-Chloro-5- (carboxaldehyde) phenylthio]-4-isopropyl- 2-methyl-1-t (4-pyridyl) methyl]-lH-pyrrole-3-ca} boxamide in 5ml of methanol was added 3mg of sodium borohydride. The mixture was stirred at room temperature for 2 h. A further 3mg of sodium borohydride was then added and the mixture stirred for 1 h. To the reaction was added 150mg of silica gel and the solvents evaporated. The product, absorbed onto silica, was purified by flash chromatography on silica gel using methanol/dichloromethane (1: 9) for the elution to give 15mg of a white solid. Mass spectrum (ESI) m/z 430 [M+H] +.

The starting material 5- [3-Chloro-5- (carboxaldehyde) phenylthio]-4-isopropyl-2- methyl-1- [ (4-pyridyl) methyl]-lH-pyrrole-3-carboxamide was prepared as follows: To a solution of 5- [3-Chloro-5-vinyl phenylthio]-4-isopropyl-2-methyl-1- [ (4- pyridyl) methyl]-lH-pyrrole-3-carboxamide in 20ml of THF, l0ml of water and 6ml of tertbutanol was added 290mg of osmium tetroxide. The mixture was stirred at room temperature for 30 min and 330mg of sodium periodate added. After 2 h 60mg of the product was precipitated as a white solid by addition of ethyl acetate/water. Mass spectrum (ESI) m/z 425 [M+H] +.

Example 127 HO HO OH 5- [3-Chloro-5- (2 (RS), 3- N dihydroxypropyl) phenylthio]-4- I isopropyl-2-methyl-1- [ (4- 127 pyridyl) methyl]-1H-pyrrole-3-474 5 carboxamide d kNH2 OU To a solution of 30mg of 4- [ [2- (3-Allyl-5-chlorophenylthio)-3-isopropyl-5-methyl- [ (4-pyrrolyl] methyl] pyridinein 7.5ml of THF, 4ml of water and lml of tert.-butanol was added 18mg of osmium tetroxide. The mixture was stirred at room temperature for 30 min and 20mg of sodium periodate added. After 2 h 15mg of the product was precipitated as a white solid by addition of diethyl ether. Mass spectrum (ESI) mlz 474 [M+H] +.

Example 141 ci 3-Chloro-5- [3-isopropyl-5- methyl-1- [ (4-pyridinyl) methyl- 141 s N 1H-pyrrol-2-ylthio] benzonitrile A mixture of 120mg of 4- [ [2- (3-Bromo-5-chlorophenylthio)-3-isopropyl-5-methyl- 1-pyrrolyl] methyl] pyridine, 96mg of copper (I) cyanide, 30mg of diphenylphosphino

ferrocene, 40mg of tetraethylammonium cyanide and 15mg of bispalladium tris (dibenzylidene acetone) were dissolved on 15ml of dioxane. The mixture was heated to 80°C for 2 h then another 96mg of copper (I) cyanide, 30mg of diphenylphosphino ferrocene, 40mg of tetraethylammonium cyanide and 15mg of bispalladium tris (dibenzylidene acetone) were added and the mixture heated for 72 h. The reaction was then cooled and The mixture was stirred at room temperature for 18 h. The orange solution was quenched with saturated sodium bicarbonate solution and extracted with ethyl acetate. The combined organic extracts were dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using petrol/ethyl acetate (1: 4 then 1: 2) then ethyl acetate for the elution to give 57mg as an oil which was further purified by HPLC to give 17mg of an oil. Mass spectrum (ESI) m/z 382 [M+H] +. STRUCTURE SYSTEMATIC Mass NAME Spectrum Ex. Reaction Scheme (m/z ES, +ve ion) Compounds were prepared analogous to reaction scheme 1: i N 5- (3, 5- ci 9 H Dichlorophenylthio) 1 using 1 using 36 N. -2, 4-dimethyl-l- [ (4- 393 ° < y"'MeCOCH2NH2 pyridyl) methyl]-1H- MeCOCH2NH2 OH pyrrole-3-methanol cl cl- Dichlorophenylthio) -4-isopropyl-2- 37 phenyl-l- [ (4- 483 PhCOCH2CO2 H) pyridyl) methyl]-lH- Et \ no pyrrole-3-methanol ci t"Dichlorophenylthio) /I Dichlorophenylthio) -4-isopropyl-2-41 1 different R1 methyl-1- [ (3- pyridyl) methyl]-lH- pyrrole-3-methanol 5- (2-chloro-4- /N fluorophenylthio)-4- ,../) isopropyl-2-methyl-1 different s 1- [ (4- disulfrde OH pyridyl) methyl]-1H- pyrrole-3-methanol 4-Isopropyl-5- (4- methoxyphenylthio) -2-methyl-1- [ (4- 1 different 40 5 N pyridyl) methyl]-lH-382 disulfide pyrrole-3-methanol OH 5- (2- CMorophenylthio)- N 4-isopropyl-2-1 different i N'- 'T, R7 methyl-l- [ (4- disul6de pyridyl) methyl]-1H- pyrrole-3-methanol F F F 5- [3- F (Trifluoromethyl) ph \ f') enylthioj-4- N enylthio]-4- 42 isoprop7l-2-methyl-420 disulfide zou pyridyl)methyl]-1H- pyrrole-3-methanol - (Trifluoromethoxy) p henylthio]-4- 43 9 e) isopropyl-2-methyl-436 1 different s \N 1- [ (4- disulfide OH pyridyl) methyl]-1H- OH pyrrole-3-methanol 5- (2, 5- Dichlorophenylthio) r\ t 44-4-isopropyl-2-421 1 different 44 methyl-1- [ (4- disulfide OH pyridyl) methyl]-lH- pyrrole-3-methanol cl 5- (3, 5- ci Dichlorophenylthio) I using "1 musing N-2, 4-diisopropyl-1- OH [ (4-pyridyl) methyl]- Et oh eut 1H-pyrrole-3- methanol 4-Isopropyl-2- methyl-5- (2- I naphthylthio)-l [ (4- I different 46 pyridinyl) methyll- 402 disulfide 1H-pyrrole-3- OH methanol el ci 5- (2, 4- Dichlorophenylthio) -4-isopropyl-2-I different 47 N421 methyl-1- [ (4-disulfide 4 \OH pyridyl) methyl]-lH- pyrrole-3-methanol 5- (3- Fluorophenylthio)- 4-isopropyl-2-1 different 48 methyl-1- [ (4-disulfide OH pyridyl) methyll-lH- pyrrole-3-methanol cle er 5-(3- 9 eJ Chlorophenylthio)-1 using 1 using 49 s N 2, 4-diisopropyl-1- 415 iPr2COCH2C0 OH [ (4-pyridyl) methyl]- oH 2Et 1H-pyrrole-3- methanol 0 4-Isopropyl-5- (3, 4- N dimethoxyphenylthi I 9 NS o)-2-methyl-1-[(4-1 different 50 N pyridyl) methyl]-lH- 412 disulfide pyrrole-3-methanol HO 4-Isopropyl-2- methyl-5- (2, 4, 6- trimethylphenylthio) 394 1 different -1- [ (4- disulfide pyridyl) methyl]-1 H- HO pyrrole-3-methanol 4-Isopropyl-2- methyl-5- (3, 4- dimethylphenylthio) 1 different -1- [ (4- disulfide pyridyl) methyl]-1H- HO pyrrole-3-methanol N 4-Isopropyl-5- (2, 5- dimethoxyphenylthi o)-2-methyl-l- [ (4- 1 different ~ pyridyl) methyl]-1H-disulfide pyrrole-3-methanol HO 4-Isopropyl-2- methyl-5- (2, 5- 5 N dimethylphenylthio) 1 different -1- [ (4- disulfide pyridyl) methyl]-1H- pyrrole-3-methanol 4-Isopropyl-5- (2- methoxyphenylthio) 55 1 s N-2-methyl-1- [ (4- 3g2 1 different pyridyl) methyl]-1H- disulfide pyrrole-3-methanol HO 5- (2- Fluorophenylthio)- 5 N 4-isopropyl-2-1 different 56 methyl-1- [ (4-disulfide ) pyridyl) methyl]-lH- PO pyrrole-3-methanol 4-Isopropyl-2- zon methyl-5- (4- t (methylphenylthio)-1 different disulfide pyridyl) methyl]-lH- \ HO pyrrole-3-methanol I-Benzyl-5- (3- cl cmorophenylthio)- 58 4-isopropyl-2-386 1 different methyl-lH-pyrrole-disulfide 3-methanol o'5-(3- ho Chlorophenylthio)- 4-isopropyl-1- (4- 1 different methoxybenzyl)-2-disulfide and Rl n H1 methyl-lH-pyrrole- 3-methanol 5- (3- ci s \ Chlorophenylthio)- 4-isopropyl-1- (3- 1 different 60 s/-. - 416 60 5 methoxybenzyl)-2-416 disulfide and RI methyl-lH-pyrrole- HO 3-methanol 1- [(5-Chloro-l- benzothiophen-3- yl) methyl]-5- (3- 6 chlorophenylthio)-476 1 different 4-isopropyl-2-disulfide methyl-lH-pyrrole- 3-methanol HO i N alpha (RS)- [5- (3, 5- cl Dichlorophenylthio) -4-isopropyl-2- 62 methyl-l- [ (4- 497 1 using PhMgBr \ HO pyridyl) methyl]-lH- pyrrol-3-yllbenzyl alcohol Chlorophenylthio)- 4-isopropyl-2- -' Idifferent 63 methyl-1- [ (4-393 1 different disulfide and R1 thiazolyl) methyl]- 1H-pyrrole-3- methanol Chlorophenylthio)- 4-isopropyl-2- ,,,,,.,, Idifferent 64 \methyl-l- [ (3- (4- 415 S. N disulfide and R1 pyridyl) propyl]-lH- pyrrole-3-methanol Ha 5- (3- Chlorophenylthio)- 4-isopropyl-2- . NIdifferent 65 4-isopropyl-2-1 different disulfide and Rl quinolyl) methyl]- Ho lH-pyrrole-3- methanol 4-Isopropyl-2- methyl-5- (2, 4- dimethylphenylthio) 1 different -1- [ (4- disulfide pyridyl) methyl]-1H- HO pyrrole-3-methanol 4-Isopropyl-2- methyl-5- (3- N methylphenylthio)-366 1 different 1- [ (4- disulfide pyridyl) methyl]-1H- WHO pyrrole-3-methanol 5- (2-Chloro-6- methylphenylthio)- 68 N 4-isopropyl-2-1 different 68- '"'401 methyl-1- [ (4-disulfide Ho Pyridyl) methyl]-lH- WO pyrrole-3-methanol F F 5- (3- N F Chlorophenylthio)- ci 1- [ [4-chloro-2- 69 (trifluoromethyl)-6-539 1 different 69 L 539 quinolyl] methyl]-4-disulfide and R1 HO isopropyl-2-methyl- lH-pyrrole-3- methanol 5- (4- Ethylphenylthio)-4- isopropyl-2-methyl-1 different 144-380 70 1- [ (4- 380 disulfide pyridyl) methyl]-1H- ß HO pyrrole-3-methanol 4-Isopropyl-5- (3- methoxyphenylthio) -2-methyl-I- [ (4-1 different 1 different 71 \5 N pyridyl) methyl]-lH-382 disulfide pyrrole-3-methanol HO ci N 5- (2, 4,6- ci Trichlorophenylthio 496 --N)-4-isopropyl-2-1 different 72 5 [M+Me methyl-1- [ (4- disulfide pyridyl) methyl]-lH- pyrrole-3-methanol N-Benzyl-2- (3- chlorophenylthio)- 4- (hydroxymethyl)- han 3-isopropyl-5-1 different 73 - r'o 443 methyl-l-disulfide and Rl 5 N pyrroleacetamide HO HO ci N F 5- (3- CI F Chlorophenylthio)- 74 s N (trifluoromethyl)-3-455 1 different pyridyl] methyl]-4- disulfide and R1 Ha isopropyl-2-methyl- lH-pyrrole-3- methanol Compounds were prepared analogous to reaction scheme 2: Cl <s [5-(3, 5-Dichloro- CI w phenylsulfanyl)-4- isopropyl-2-methyl- 75 J o l-pyridin-4-493 ketone) ylmethyl-lH-pyrrol- \ HO P < 3-yl]-hydroxy-acetlc acid ethyl ester cl, cl N N- [f5- (3, 5- ci Dichlorophenylthio) 5 N -4-isopropyl-2- 76 \.-b methyl-1- [ (4- 525 2 o pyridyl) methyl]-lH- pyrrol-3-yl] methyll- 4-pyridineacetamide CI/N ci ci 2-Acetamido-N- [ [5- (3, 5- dichlorophenylthio)- 4-isopropyl-2- methyM- [ (4- pyridyl)methyl]-1H- pyrrol-3- yl] methyl] acetamide CI/N cm. N- [ [5- (3, 5- 1 Dichlorophenylthio) -4-isopropyl-2- methyl-l- [ (4- 78'oJ''574 2 pyridyl) methyl]-1H- pyrrol-3-yl] methyl]- p toluenesulfonamide X @ tert. butyl [ [ [ [5- (3, 5- dichlorophenylthio)- 0 4-isopropyl-2- 79 methyl_ 1- [ (4- 577 2 pyridyl)methyl]-1H- pyrrol-3- yl] methyls carbamoyl ] methyl] carbamate N2- [ [5- (3, 5- cmr I 9 e) Dichlorophenylthio) -4-isopropyl-2- methyl-1- [ (4-477 2 80- (-R'477 2 O\NH2 pyridyl) methyl]-1H- p"NHz pyrrol-3- yl] methyl] glycinami de ci N_5_3'S_- c Dichlorophenylthio) -4-isopropyl-2- 81 methyl-l- [ (4- 498 2 81 pyridyl) methyl-1H- pyrrol-3- yl] methyl] methanes ulfonamide N Phenyl [ [5- (3, 5- ci 1 I dichlorophenylthio)- S N 4-isopropyl-2- 82 oN methyl-1- [ (4- 540 2 pyridyl) methyl]-1H- pyrrol-3- pYr yl] methyl] carbamate Cl 8 eN Methyl [ [5- (3, 5- dichlorophenylthio)- 4-isopropyl-2- 83 < methyl-1-[(4-478 2 pyridyl) methyl]-lH- oF \ pyrrol-3- yl] methyls carbamate ci """ N-5- (3, 5- Dichlorophenylthio) 5 N -4-isopropyl-2- methyl-l- [ (4- id 1 meth 1-1H-560 2 o PYr Y Y pyrrol-3- yl]methyljbenzenesu Ifonamide ci N Nl-Acetyl-0-tert.- butyl-N2- [ [5- (3, 5- \. N dichlorophenylthio)- 4-isopropyl-2- S5 \) r< ° J., r.. 605 2 Ó/) methyl-1-[(4- pyridyl) methyl]-lH- pyrrol-3-ylmethyl]- L-serinamide Nl-Acetyl-N2- [ [5- cl 1 (3, 5- N dichlorophenylthio)- 4-isopropyl-2- 86 \ \- (, o J-. 549 2 ) methyl-1- [ (4- HO pyridyl) methyl]-1H- pyrrol-3-yl]methyl- L-serinamide N1- (tert.- j butoxycarbonyl)-O- tert.-butyl-N2- [ [5- 0 (3, 5- dichlorophenylthio)- 87/r* 663 2 4-isopropyl-2- methyl-1-[(4- pyridyl)methyl]-1H- pyrrol-3-yl] methyl]- L-serinamide Cl 1- [ [5- (3, 5- c w Dichlorophenylthio) -4-isopropyl-2- 88 - H methyl-l- [ (4- 491 2 a Ls/pyridyl) methyll-lH- pyrrol-3-yl] methyl]- 3,3-dimethylurea ci N 1- [ [5- (3, 5- Dichlorophenylthio) S N 5-4-isopropyl-2- 89 methyl-l- [ (4- 553 2 Ok \ pyriyl) methyl]-lH- pyrrol-3-yl] methyl]- 3-methyl-3- phenylurea cl "1_ (5- (3, 5- cl Dichlorophenylthio) -4-isopropyl-2- 90 XN methyl-1- [ (4-463 2 h-NH2 pyridYI) methyl]-IH- 0 pyrrol-3- yl] methyls urea I 0" 4- [ [2- (3, 5- cl w Dichlorophenylthio) -3-isopropyl-4- 91 xi (methoxymethyl)-5-435 2 > methyl-1- pyrrolyl] methyl] pyri dine 4- [ [2- (3- Chlorophenylthio)- N 3-isopropyl-4- (methoxymethyl)-5-401 2 methyl-1- pyrrolyl] methyl] pyri dine N 4- [ [3- (Azidomethyl)-5- s-y-- (3, 5- 93 SNNN dichlorophenylthio)-446 2 93 /\. N==N=N ''446 2 4-isopropyl-2- methyl-1- pyrrolyl] methyl] pyri dine cl "N_ (5-35- ci " Dichlorophenylthio) -4-isopropyl-2- 94 methyl-I-f (4-462 2 pyridyl) methyl]-lH- pyrrol-3- yl] methyl] acetamide cl--qcl 4- [ [2- (3, 5- ci Dichlorophenylthio) 95 5 N-3-isopropyl-5-417 2 95 417 2 methyl-4-vinyl-l- % pyrrolyl] methyl] pyri dine i N 1 (RS)- [5- (3, 5- cl S CJ Dichlorophenylthio) 5-4-isopropyl-2-2 96 methyl-1- [ (4-451 ß f OH pyridyl) methyl]-lH-from vinyl pyrrol-3-yl]-1, 2- ethanediol N- [ [5- (3, 5- cri Dichlorophenylthio) 'N s-4-isopropyl-2- 97 methyl-1- [ (4- 9 524 2 Ó/pyridyl) methyl]-1H- pyrrol-3- yl] methyl] benzamid e Br 8 er tert.-butyl 5-(3- Br bromo-5- chlorophenylthio)- 4-isopropyl-2-2 tBu only 9g o 536 methyl-l- [ (4- difference pyridyl) methyl]-lH- pyrrole-3- carboxylate Br 8 er tert.-butyl 5-(3,5- Br dibromophenylthio) -4-isopropyl-2- 2 tBu only 99 methyl-1- [ (4-580 /\-r). i i i difference pyridyl) methyl]-lH- /pyrrole-3- i carboxylate Compounds were prepared analogous to reaction scheme 3: ci," cl Dichlorophenylthio) -4-isopropyl-2-3 using 100 F methyl-l- [ (4- 487 CF3COCH2CO FF pyridyl) methyl]-lH-2Et pyrrol-3-yl]-2,2,2- trifluoroethanone ci ci 1- [5- (3, 5- cl w 9 tJ Dichlorophenylthio) 3 using 3 using '. N.-4-isopropyl-2- N-4-isopropyl-2- methyl-1- (4- -pyridyl) methyl]-lH- pyrrol-3-yl] ethanone Ber/" Br Dibromophenylthio) -4-isopropyl-2- 102 \\ 1l methyl-1-[(4-523 NH2COCH2C0 NH2 pyridyl) methyl]-lH- 2Et O pyrrole-3- carboxamide 4-Isopropyl-5- (3, 5- dimethoxyphenylthi 3 using different 9 NC o)-2-methyl-1-[(4-disulfide and 103 sY 41 pyridyl) methyl]-1H-425 NH2COCH2CO pyrrole-3-2Et ?,--NH carboxamide Brs 5-(3-Bromo-5- B t H) chlorophenylthio)- 4-isopropyl-2- 104 J'methyl-l- [ (4- 480 ,/-\u, NH2COCH2CO eNH2 pyridyl) methyl]-1H-2Et 2Et pyrrole-3- carboxamide Ethyl 5- (3, 5- dichlorophenylthio)- N 4-isopropyl-2-3 using 105 ß p methyl-1- [(4-491 EtO2CCOCH2C -y pyridyl) methyl]-lH- 02Et o pyrrole-3-glyoxalate N\ er 5-(3- Cyanophenylthio)- sw s7 4-isopropyl-2-disulfide and '/r,,, disulfideand 106 \ methyl-1-4-390 > 'pyridyl) methyl]-lH- \ o 2Et pyrrole-3- carboxamide Compounds were prepared analogous to reaction scheme 6 or 7: 5- (3- Chlorophenylthio)- 2- (hydroxymethyl)- 4-isopropyl- 107/\ 417 6 alpha (RS)-methyl-l- PO [ (4-pyridyl) methyl- lH-pyrrole-3- ethanol ei f"or 5- (3, 5- Dichlorophenylthio) -3- (hydroxymethyl)- w 108 0 4-isopropyl-l- [ (4- 438 6 H pyridyl) methyl]-lH- pyrrole-2- carboxaldehyde cl w c i ( 5- (3, 5- Dichlorophenylthio) N-4-isopropyl-1- [ (4- 109"<) ro 433 6 J ° pyridyl) methyl]-lH- pyrrole-2, 3- dicarboxaldehyde cl 5- (3, 5- Dichlorophenylthio) -3- (hydroxymethyl)- 110 OH 4-isopropyl-451 6 ..-oH lpha (RS)-methyl-1- [ (4-pyridyl) methyl]- lH-pyrrole-2- ethanol cl. Dichlorophenylthio) N-4-isopropyl-1- [ (3- 4376 ~t/4 OH pyridyl] methyl]-1H- OH pyrrole-2,3- dimethanol Compounds were prepared analogous to reaction scheme 8 or 9: cl (3, 5- cl Dichlorophenylthio) 112-4-isopropyl-l- [ (4-407 8 pyridyl) methyl]-1H- pyrrole-2-methanol ci [5- (3,5- Dichlorophenylthio) -4-isopropyl-l- [ (4- 113 LJ/°pyridyl) methyl]-lH- g pyrrol-2-yl] methyl acetate cl cl, Dichlorophenylthio) 113a s N-4-isopropyl-1- [ (4-405 8 /° pyridyl) methyl-1H- pyrrole-2- carbaldehyde ci 4- [5- (3, 5-Dichloro- cl phenylsulfanyl)-4- 0 isopropyl-l-pyridin- 114 4-ylmethyl-lH-445 8 pyrrol-2-yl]-but-3- en-2-one cl N 4y2- (35- c Dichlorophenylthio) -5-methyl-3-phenyl- v 1- pyrrolyl] methyl) pyri dine -pyrrolyllmethyllpyri dine 1 e Dichlorophenylthio) -3-isopropyl-5- 115a ',, 391 8 methyl-1- ß pyrrolyl] methyl] pyri dine ci cl-5- (3,5- Dichlorophenylthio) -N- (2, 4, 6- trimethoxybenzyl)- 116 2-methyl-4-phenyl-648 8 1- [ (4- pyridyl)methyl]-1 H- pyrrole-3- carboxamide cl +c er 5-(35- Dichlorophenylthio) -2-methyl-4-phenyl- 1- ( (4- C ot pyridyl) methyl3-lH- 0 pyrrole-3-carboxylic acidtrifluoroacetate (1: 1) , N 5- (3, 5- cl Dichlorophenylthio) 5 N-4-phenyl-2-methyl- 118 1- [ (4- 468 8 NH2 pyridyl) methyl]-lH- pyrrole-3- carboxamide ci 5- (3, 5- Dichlorophenylthio) -2-methyl-4-phenyl- 119 1- [ (4- 450 8 C WN pyridyl) methyl]-lH- N pyrrole-3- carbonitrile ci cl 5- (3, 5- Dichlorophenylthio) -4-isopropyl-N, 2- 120 dimethyl-l- [ (4- 448 8 pyridyl) methyl]-lH- pyrrole-3- carboxamide cri, cl Dichlorophenylthio) -4-cyclopropyl-2- 121 methyl-1- [ (4-432 8 pyridyl) methyl]-lH- i/ pyrrole-3- carboxamide cl, n 5- (3, 5- Dichlorophenylthio) -4-isopropyl-2- 122 methyl-l- [ (4- 510 8 b pyridyl) methyl]-lH- pyrrole-3- carboxanilide ci 5- (3, 5- ci Dichlorophenylthio) -4-isopropyl-N, N, 2- 123 trimethyl-l- [ (4- 462 8 pyridyl) methyl]-lH- pyrrole-3- carboxamide ci 5- (3-Allyl-5- chlorophenylthio)- 4-isopropyl-2- 124 s X methyl-1-[(4-440 8 NH2 pyridyl) methyl]-1H- 0 o pyrrole-3- carboxamide ci N 5- (3-Chloro-5- propylphenylthio)- 4-isopropyl-2- N 125 5 methyl-1- [ (4-442 8 pyridyl) methyl]-lH- pyrrole-3- carboxamide ci 5- (3-Chloro-5- vinylphenylthio)-4- isopropyl-2-methyl- s 126 1- [ (4- 426 8 NH2 pyridyl) methyl]-1H- OU pyrrole-3- carboxamide HO HO OH 5- [3-Chloro-5- ci (2 (RS), 3- dihydroxypropyl) ph N enylthio]-4- 127 isopropyl-2-methyl-474 8 o,.-NHz 1-L pyridyl)methyl]-1H- pyrrole-3- carboxamide 4- [ [2- (3, 5- cul 9 e) Dichlorophenylthio) -5- (ethoxymethyl)- 128 wo 3-isopropyl-1-435 8 pyrrolyl] methyl] pyri dine ci N 4- [ [2- (3, 5- ci td Dichlorophenylthio) -3-isopropyl-5- 129 421 8. (methoxymethyl)-1- > pyrrolyl] methyl] pyri dine ct Cl/8 N (5_ (35_ ijichlorophenylthio) 0 0 4-isopropyl-l- [ (4- 130 0 NH, 450 8 pyridyl) methyl]-1 H- \ pyrrol-2-yl] methyl carbamate Br/cr 4-[12-(3-Bromo-5- Br chlorophenylthio)- N 3-isopropyl-5- 131 435 8 methyl-1- \ pyrrolyl] methyl] pyri dine Compounds were prepared analogous to reaction scheme 10 4- [ [2- (3-Allyl-5- , chlorophenylthio)- 3-isopropyl-5-397 10 132 s... 397 10 methyl- [ (4- pyrrolyl] methyl] pyri dine 4- [ [2- (3-Chloro-5- propylphenylthio)- 3-isopropyl-5- methyl-l- "\ methyl-1- pyrrolyl] methyl] pyri dine 5- (3-Chloro-5- ethylphenylthio)-4- N isopropyl-2-methyl- s 134 1- [ (4- 428 10- NH, pyridyl) methyl]-lH- pyrrole-3- carboxamide 5- [3-Chloro-5- (hydroxymethyl) phe N nylthio]-4- s 135 XNH2 isopropyl-2-methyl-430 10 -NHZ 1-4_ pyridyl) methyl]-1H- pyrrole-3- carboxamide Biphenylylthio)-4- 136 C s_t isopropyl-2-methyl-428 10 pyridyl) methyl]-1H- HO pyrrol-3-methanol Biphenylylthio)-4- isopropyl-2-methyl- 137 1- [ (4- 428 10 pyridyl) methyl]-1H- HO pyrrole-3-methanol 4-Isopropyl-2- methyl-1- [ (4- pyridyl) methyl]-5- il8 N [2- (3- 429 10 pyridyl) phenylthio]- HO lH-pyrrole-3- methanol 5- [2- HO_4 9 (Hydroxymethyl) ph enylthio]-4- 139 isopropyl-2-methyl-382 10 1- [ (4- pyridyl) methyl]-1 H- pyrrole-3-methanol Cl 5- (5-Chloro-3- biphenylylthio)-4- N isopropyl-2-methyl- s 140 1- [ (4- 476 10 ß ok 2 pyridyl) methyl]-lH- : : po pyrrole-3- carboxamide N. iCi 3-Chloro-5- [3- isopropyl-5-methyl- 141 382 10 kb pyridinyl) methyl]- % lH-pyrrol-2- ylthio] benzonitrile N 5- [3-Isopropyl-5- N methyl-1- (4- pyridyl) methyl]-1H- s X pyrrol-2-ylthio]-1, 3- dibenzonitrile