Radiolabeled compounds

Abstract

The present invention relates to radiolabeled compounds of formula I ##STR00001##
wherein either A, B, R.sub.1, R.sub.2, is labeled with a radionuclide selected from .sup.3H, .sup.11C and .sup.18F and its use for imaging alpha synuclein and/or Abeta deposits in mammals.

Claims

1. A method of imaging alpha synuclein and/or Abeta deposits in a brain of a mammal, comprising: introducing into a mammal a detectable quantity of a radiolabeled compound selected from the group consisting of: 2-Fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide 4-Hydroxy-N-[4-[4-(2-pyridyl)piperazin-1-yl]phenyl]benzamide 4-Methoxy-N-[4-(4-pyridin-2-ylpiperazin-1-yl)phenyl]benzamide 6-Methoxy-N-[4-[4-(5-methyl-2-pyridyl)piperazin-1-yl]phenyl]pyridine-3-carboxamide 4-Methyl-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide 4-(4-Methylpiperazin-1-yl)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide 4-(Dimethylamino)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide 4-Morpholino-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide 2-Fluoro-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide 2-Fluoro-4-methyl-N-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide 4-Methoxy-2-methyl-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide 4-(2-(2-Fluoroethoxy)ethoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide 4-Methoxy-N-[4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]benzamide N-(4-(4-(Pyridin-2-yl)piperazin-1-yl)phenyl)-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxamide N-(4-(4-(Pyridin-2-yl)piperazin-1-yl)phenyl)benzo[d][1,3]dioxole-5-carboxamide N-(4-(4-(Pyridin-2-yl)piperazin-1-yl)phenyl)imidazo[1,2-a]pyridine-7-carboxamide N-(4-(4-(Pyridin-2-yl)piperazin-1-yl)phenyl)imidazo[1,2-a]pyridine-6-carboxamide 2-Fluoro-4-methoxy-N-[4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]benzamide 4-Methoxy-2-methyl-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide 4-(Dimethylamino)-N-[4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]benzamide 2-Fluoro-4-methyl-N-[4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]benzamide 4-(4-Methylpiperazin-1-yl)-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide 2-Fluoro-4-methyl-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide 4-Methoxy-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide 5-Methyl-N-[4[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]pyridine-2-carboxamide 4-Morpholin-4-yl-N-[4[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]benzamide 4-Methyl-N-[4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]benzamide 4-(4-Methylpiperazin-1-yl)-N-[4[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]benzamide 2-Fluoro-4-methoxy-N-[2-methyl-4[4-(2-pyridyl)piperazin-1-yl]phenyl]benzamide 4-(Dimethylamino)-N-[4[4-(6-methyl-2-pyridyl)piperazin-1-yl]phenyl]benzamide 4-(Dimethylamino)-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide 4-Morpholino-N-6[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide 5-Methyl-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]pyridine-2-carboxamide 2-Fluoro-4-methoxy-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide 4-Methyl-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide 4-(Dimethylamino)-N-[6-[4-(2-pyridyl)piperazin-1-yl]pyridazin-3-yl]benzamide 4-Methyl-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide 4-Methoxy-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide 4-Morpholino-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide 2-Fluoro-4-methoxy-N-[6-[4-(2-pyridyl)piperazin-1-yl]pyridazin-3-yl]benzamide 4-Methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide 4-Methyl-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)-3,4-dihydro-2H-benzo[b] [1,4] oxazine-7-carboxamide 4-Methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide 2-Fluoro-4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide 4-Methyl-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide 4-(Dimethylamino)-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide 2-Fluoro-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide 4-Morpholino-N-[6-[4-(2-pyridyl)piperazin-1-yl]pyridazin-3-yl]benzamide 4-Methoxy-N-{4-[4-(pyrimidin-2-yl)piperazin-1-yl]phenyl}benzamide N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide 4-Morpholino-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide 2-Fluoro-4-methyl-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide 5-Methyl-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)picolinamide 3-Methyl-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide 4-Methoxy-N-{4-[4-(1,3,5-triazin-2-yl)piperazin-1-yl]phenyl}benzamide 4-Methoxy-N-{4-[4-(pyrimidin-4-yl)piperazin-1-yl]phenyl}benzamide N-[4-[4-(4-Cyanophenyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide 4-Methoxy-N-[4-[4-(6-methoxypyridin-3-yl)piperazin-1-yl]phenyl]benzamide 4-Methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide 2-Fluoro-4-methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide 2-Fluoro-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide 4-(Dimethylamino)-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide 4-Morpholino-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide 3-Methyl-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide N-[4-[4-(4-Cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide 4-Methoxy-N-{4-[4-(thiophen-2-yl)piperazin-1-yl]phenyl}benzamide 4-Methoxy-N-{4-[4-(2-methoxypyridin-3-yl)piperazin-1-yl]phenyl}benzamide 4-Methoxy-N-{4-[4-(6-methoxypyridin-2-yl)piperazin-1-yl]phenyl}benzamide 4-Methoxy-N-{4-[4-(2-methoxyphenyl)piperazin-1-yl]phenyl}benzamide N-{4-[4-(2-Cyanophenyl)piperazin-1-yl]phenyl 1-4-methoxybenzamide N-{4-[4-(2-Fluorophenyl)piperazin-1-yl]phenyl 1-4-methoxybenzamide 4-Methoxy-2-methyl-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide 4-(4-Methylpiperazin-1-yl)-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide 4-Methyl-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide 5-Methyl-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)picolinamide 5-Methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)picolinamide 5-Methoxy-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)picolinamide 5-Methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)picolinamide 5-Methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)picolinamide 4-Methoxy-2-methyl-N-[5-(4-pyridin-2-ylpiperazin-1-yl)pyridin-2-yl]benzamide 4-(4-Methylpiperazin-1-yl)-N-5-(4-pyridin-2-ylpiperazin-1-yl)pyridin-2-yl]benzamide 4-Methoxy-N-[4-[4-(4-methoxy-2-pyridyl)piperazin-1-yl]phenyl]benzamide Acetic acid; 4-Methoxy-N-[4-[4-(3-methyl-4-pyridyl)piperazin-1-yl]phenyl]benzamide 2-Fluoro-4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide 4-Methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide 4-(Dimethylamino)-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide 4-(4-Methylpiperazin-1-yl)-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide 4-Morpholino-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide 4-Methyl-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide 5-Methyl-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)picolinamide N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-6-methoxypicolinamide N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-4-morpholinobenzamide N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-6-methoxypicolinamide 4-Morpholino-N-(4-(4-(thiophen-2-yl)piperazin-1-yl)phenyl)benzamide N-(5-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)pyridin-2-yl)-4-methoxybenzamide N-(5-(4-(4-Cyanophenyl)piperazin-1-yl)pyridin-2-yl)-4-methoxybenzamide N-(2-(4-(4-Cyanophenyl)piperazin-1-yl)pyrimidin-5-yl)-4-methoxybenzamide N-(2-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)-4-methoxybenzamide N-(2-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)-4-morpholinobenzamide N-[4-[4-(6-Cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide 4-Methoxy-N-[4-(4-phenylpiperazin-1-yl)phenyl]benzamide 4-Methoxy-N-[4-[4-(4-methyl-2-pyridyl)piperazin-1-yl]phenyl]benzamide N-[4-[4-(3-Cyanophenyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide N-[4-[4-(3-Fluorophenyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide N-[4-[4-(4-Fluorophenyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide N-[3-Fluoro-4-[4-(2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide N-[4-[4-(5-Cyano-2-pyridyl)piperazin-1-yl]-3-fluoro-phenyl]-4-methoxy-benzamide N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-hydroxybenzamide 4-Methoxy-N-[4-[4-(p-tolyl)piperazin-1-yl]phenyl]benzamide 4-Methoxy-N-[4-[4-(4-methoxyphenyl)piperazin-1-yl]phenyl]benzamide 4-Methoxy-N-[4-[4-(4-methylsulfonylphenyl)piperazin-1-yl]phenyl]benzamide N-[4-[4-(4-Cyanophenyl)piperazin-1-yl]-3-methyl-phenyl]-4-methoxy-benzamide N-[4-[4-(5-Cyano-2-pyridyl)piperazin-1-yl]-3-methyl-phenyl]-4-methoxy-benzamide N-[4-[4-(4-Cyanophenyl)piperazin-1-yl]phenyl]-2-fluoro-4-methoxy-benzamide N-[4-[4-(5-Cyano-2-pyridyl)piperazin-1-yl]phenyl]-2-fluoro-4-methoxy-benzamide N-[4-[4-(5-Cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-(2-fluoroethoxy)benzamide N-[4-[4-(4-Cyanophenyl)piperazin-1-yl]phenyl]-4-(2-fluoroethoxy)benzamide 4-(2-Fluoroethoxy)-N-[4-[4-(2-pyridyl)piperazin-1-yl]phenyl]benzamide 4-(2-Fluoroethoxy)-N-[4-(4-thiazol-2-ylpiperazin-1-yl)phenyl]benzamide 4-[2-[2-(2-Fluoroethoxy)ethoxy] ethoxy]-N-[4-(4-thiazol-2-ylpiperazin-1-yl)phenyl]benzamide N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-(2-(2-fluoroethoxy)ethoxy)benzamide N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-4-(2-(2-fluoroethoxy)ethoxy)benzamide N-[4-[4-(4-Cyanophenyl)piperazin-1-yl]phenyl]-4-[2-[2-(2-fluoroethoxy)ethoxy]ethoxy]benzamide rac-4-(2-((tert-Butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide rac-4-(3-Fluoro-2-hydroxypropoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide rac-4-(2-((tert-Butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(thiazol-2-yl)piperazin-1-yl)phenyl)benzamide rac-4-(2-((tert-Butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(4-cyanophenyl)piperazin-1-yl)phenyl)benzamide rac-4-(2-((tert-Butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(4-cyanopyridin-2-yl)piperazin-1-yl)phenyl)benzamide rac-N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-(3-fluoro-2-hydroxypropoxy)benzamide rac-4-(3-Fluoro-2-hydroxypropoxy)-N-(4-(4-(thiazol-2-yl)piperazin-1-yl)phenyl)benzamide rac-N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-4-(3-fluoro-2-hydroxypropoxy)benzamide 4-Methoxy-N-(4-((3 aS,6aS)-5-(pyridin-2-yl)hexahydropyrrolo [3,4-c]pyrrol-2(1H)-yl)phenyl)benzamide 4-Methoxy-N-(4-((3aR,6aR)-5-(pyridin-2-yl)hexahydropyrrolo [3,4-c]pyrrol-2(1H)-yl)phenyl)benzamide 4-(Fluoromethoxy)-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide 4-(Fluoromethoxy)-N-[4-(4-pyridin-2-ylpiperazin-1-yl)phenyl]benzamide N-[4-[4-(5-Cyanopyridin-2-yl)piperazin-1-yl]phenyl]-4-(fluoromethoxy)benzamide 4-(2-(2-Hydroxyethoxy)ethoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide 4-Hydroxy-N-[4-(4-pyridin-3-ylpiperazin-1-yl)phenyl]benzamide N-(4-(4-(4-Cyano-2-methoxyphenyl)piperazin-1-yl)phenyl)-4-methoxybenzamide N-(4-(4-(4-Cyano-3-methoxyphenyl)piperazin-1-yl)phenyl)-4-methoxybenzamide N-(4-(4-(5-Fluoropyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide N-(4-(4-(5-(Dimethylamino)pyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide N-(4-(4-(5-Cyanopyrimidin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide N-(4-(4-(4-Cyano-2-methylphenyl)piperazin-1-yl)phenyl)-4-methoxybenzamide N-(4-(4-(4-Cyano-2-fluorophenyl)piperazin-1-yl)phenyl)-4-methoxybenzamide N-(4-(4-(6-Fluoropyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide N-(4-(4-(5-Cyanopyrazin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide N-(4-(4-(3-Fluoropyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide N-(4-(4-(4-Chloropyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide N-(4-(4-(4-Cyano-3-fluorophenyl)piperazin-1-yl)phenyl)-4-methoxybenzamide N-(4-(4-(5-Cyano-4-methylpyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide N-(4-(4-(4-Chloro-5-cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide N-(4-(4-(4-Cyano-3-methylphenyl)piperazin-1-yl)phenyl)-4-methoxybenzamide N-(4-(4-(6-Cyanopyridin-3-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide 4-Methoxy-N-(4-(4-(2-methoxypyridin-4-yl)piperazin-1-yl)phenyl)benzamide 4-Methoxy-N-(4-(4-(6-methylpyridin-3-yl)piperazin-1-yl)phenyl)benzamide N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-6-methoxynicotinamide N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-1-methyl-1H-pyrazole-4-carboxamide N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-3,4-dimethoxybenzamide N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-3-fluoro-4-methoxybenzamide N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)isonicotinamide N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-5-methoxypicolinamide N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-3-fluoro-4-methoxybenzamide 4-Cyano-N-(4-(4-(5-cyanopyridin-2-yl)piperazin-1-yl)phenyl)benzamide N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)pyrimidine-4-carboxamide N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-5-methoxypicolinamide N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-4-methoxy-3-methylbenzamide N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-4-methoxy-2-methylbenzamide N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-3,4-dimethoxybenzamide N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxy-3-methylbenzamide N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-6-methoxynicotinamide Methyl 6-(4-(4-(4-methoxybenzamido)phenyl)piperazin-1-yl)nicotinate N-(4-(4-(6-Cyanopyridin-3-yl)piperazin-1-yl)phenyl)-5-methoxypicolinamide N-[4-[4-(5-Cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-prop-2-ynoxy-benzamide N-[4-[4-(5-Cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-(2-prop-2-ynoxyethoxy)benzamide N-[4-[4-(5-Ethynyl-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide 4-Prop-2-ynoxy-N-[4-[4-(2-pyridyl)piperazin-1-yl]phenyl]benzamide and 4-(2-Prop-2-ynoxyethoxy)-N-[4-[4-(2-pyridyl)piperazin-1-yl]phenyl]benzamide, wherein the compounds are labeled with the radionuclide .sup.3H.

2. The method of claim 1, wherein the radiolabeled compound is selected from the group consisting of: 2-Fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide 4-Methoxy-N-[4-(4-pyridin-2-ylpiperazin-1-yl)phenyl]benzamide 4-(2-(2-Fluoroethoxy)ethoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-(2-(2-fluoroethoxy)ethoxy)benzamide N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-4-(2-(2-fluoroethoxy)ethoxy)benzamide 4-(Fluoromethoxy)-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide 4-(Fluoromethoxy)-N-[4-(4-pyridin-2-ylpiperazin-1-yl)phenyl]benzamide and N-[4-[4-(5-Cyanopyridin-2-yl)piperazin-1-yl]phenyl]-4-(fluoromethoxy)benzamide, wherein the compounds are labeled with the radionuclide .sup.3H.

3. The method of claim 1, wherein the radiolabeled compound is selected from the group consisting of: ##STR00309##

4. The method of claim 1, wherein the radiolabeled compound is in a pharmaceutical composition further comprising a pharmaceutical acceptable carrier.

Description

SHORT DESCRIPTION OF THE FIGURES

(1) FIG. 1: Binding of radioligand [.sup.3H]Example-3 binding (3 nM) to A30P transgenic mouse brain sections (top left) and human PD cortical tissue sections (top middle) showing good co-localization with the anti-aSyn mAb pS129 (bottom). At higher magnification, hot spots of the autoradiograms show good co-localization with LBs stained by the aSyn mAb pS129 (right image, arrows).

(2) FIG. 2: Principle of the in vitro displacement screening assay using the specific binding of the screening radioligand [.sup.3H]Example-3 to A30P transgenic mouse brain sections and assessing the displacement potency of novel compounds. Maximal displacement (100%) is defined by co-incubation with 3 μM cold compound Example 3.

(3) FIG. 3: In vitro displacement screening results of six novel compounds showing high affinity for aSyn aggregates in A30P transgenic mouse brain sections.

(4) FIG. 4: In vitro autoradiography of tritiated compounds which have been identified as high affinity displacers in the screening assay. All ligands (at 10 nM) show strong binding to aSyn in A30P transgenic mouse brain sections.

(5) FIG. 5: Ex vivo autoradiography of tritiated compounds after i.v. injection in A30P mice and sacrificing the animal at 30 min p.i.

(6) FIG. 6: Principle of the Aβ counterscreen based on an in vitro displacement assay using the specific binding of the screening radioligand [.sup.3H]Example 3 to human AD brain sections and assessing the displacement potency of novel compounds. Maximal displacement (100%) is defined by co-incubation with 3 μM cold compound Example 3.

(7) FIG. 7: In vitro autoradiography of AD tissue sections using tritiated compounds which have been identified as high affinity displacers in the A30P screening assay. All ligands (at 10 nM) show strong binding to Aβ in human AD brain sections.

(8) FIG. 8: Binding of radioligand [.sup.3H]Example 134 (3 nM) to a human AD cortical tissue section showing an autoradiographical distribution pattern (left) which corresponds to the staining pattern of an anti-AD mAb (middle). Merged images of autoradiography and immunohistochemistry show co-localization of hot spots of the autoradiograms with Aβ plaques stained by an Aβ mAb (right).

DETAILED DESCRIPTION OF THE INVENTION

Definitions

(9) Unless otherwise indicated, the following definitions are set forth to illustrate and define the meaning and scope of the various terms used to describe the invention herein.

(10) The terms “compound(s) of the formula (I)”, “compound(s) of formula (I)”, “compound(s) of this invention” or “compound(s) of the present invention” refer to any compound selected from the genus of compounds as defined by the formula (I) including stereoisomers, tautomers, solvates, and salts (e.g. pharmaceutically acceptable salts) thereof.

(11) It must be noted that, as used in the specification and the claims, the singular forms “a”, “an” and “the” include plural referents unless the context clearly dictates otherwise.

(12) The use of “or” or “and” means “and/or” unless stated otherwise.

(13) When indicating the number of, the term “one or more” means from one substituent to the highest chemically? possible number of substitution, i.e. replacement of one hydrogen up to replacement of all hydrogens by substituents.

(14) The term “optional” or “optionally” denotes that a subsequently described event or circumstance may but need not occur, and that the description includes instances where the event or circumstance occurs and instances in which it does not.

(15) Any formula given herein is also intended to represent isotopically labeled forms of the compounds. Isotopically labeled compounds have structures depicted by the formulas given herein except that one or more atoms are replaced by an atom having a selected atomic mass or mass number. Examples of isotopes that can be incorporated into compounds of the invention include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, fluorine, chlorine, and iodine, such as .sup.2H, .sup.3H, .sup.11C, .sup.13C, .sup.14C, .sup.15N, .sup.18O, .sup.17O, .sup.31P, .sup.32P, .sup.35S, .sup.18F, .sup.36Cl, and .sup.125I, respectively. Substitution with heavier isotopes such as deuterium (i.e., .sup.2H) may afford certain therapeutic advantages resulting from greater metabolic stability, for example increased in vivo half-life or reduced dosage requirements. Substitution with .sup.2H may in particular be used to prevent the formation of undesired radiometabolites or to block radiodefluorination. Isotopically labeled compounds of this invention and prodrugs thereof can generally be prepared by carrying out the procedures disclosed in the schemes or in the examples and preparations described below by substituting a readily available isotopically labeled reagent for a non-isotopically labeled reagent. Furthermore, several methods exist for incorporating .sup.11C (Peter J. H. Scott, Angew. Chem. Int. Ed. 2009, 48, 6001-6004) or .sup.18F (Sean Preshlock et al., Chem. Rev. 2016, 116, 719-766. Frederic Dolle (2008) Fluorine-18 chemistry for molecular imaging with positron emission tomography. In Fluorine and Health: Molecular Imaging, Biomedical Materials and Pharmaceuticals (Tressaud, A. and Haufe, G., eds), pp. 3-66, Elsevier) into compounds.

(16) The term “substituent” denotes an atom or a group of atoms replacing a hydrogen atom on the parent molecule.

(17) The term “halogen” refers to fluorine, chlorine, bromine and iodine, and in some embodiments more specifically fluorine, chlorine and bromine.

(18) The term “alkoxy” denotes a group of the formula —O—R′, wherein R′ is an alkyl group. Examples of alkoxy moieties include methoxy, ethoxy, isopropoxy, and tert-butoxy.

(19) The term “alkyl” denotes a monovalent linear or branched saturated hydrocarbon group of 1 to 12 carbon atoms. In particular embodiments, alkyl has 1 to 7 carbon atoms, and in more particular embodiments 1 to 4 carbon atoms. Examples of alkyl include methyl, ethyl, propyl, isopropyl, n-butyl, iso-butyl, sec-butyl, or tert-butyl.

(20) The term “alkynyl” denotes a monovalent linear or branched hydrocarbon group of 2 to 12 carbon atoms with at least one triple bond. In particular embodiments, alkynyl has 2 to 7 carbon atoms, and in more particular embodiments 2 to 4 carbon atoms. Examples of alkynyl groups include ethynyl and propynyl.

(21) The term“alkynoxy” denotes a group of the formula —O—R′, wherein R′ is an alkynyl group.

(22) The term “aromatic” denotes the conventional idea of aromaticity as defined in the literature, in particular in IUPAC—Compendium of Chemical Terminology, 2nd, A. D. McNaught & A. Wilkinson (Eds). Blackwell Scientific Publications, Oxford (1997).

(23) The term “aryl” denotes a monovalent aromatic carbocyclic mono- or bicyclic ring system comprising 6 to 10 carbon ring atoms. Examples of aryl moieties include phenyl and naphthyl.

(24) The term “haloalkoxy” denotes an alkoxy group wherein at least one of the hydrogen atoms of the alkoxy group has been replaced by same or different halogen atoms, particularly fluoro atoms. Examples of haloalkoxyl include monofluoro-, difluoro- or trifluoro-methoxy, -ethoxy or -propoxy, for example 3,3,3-trifluoropropoxy, 2-fluoroethoxy, 2,2,2-trifluoroethoxy, fluoromethoxy, or trifluoromethoxy. The term “perhaloalkoxy” denotes an alkoxy group where all hydrogen atoms of the alkoxy group have been replaced by the same or different halogen atoms.

(25) The term “hydroxyl-haloalkoxy” denotes an haloalkoxy group wherein at least one of the hydrogen atoms of the haloalkoxy group has been replaced by a hydroxyl group.

(26) The term “heteroaryl” denotes a monovalent aromatic heterocyclic mono- or bicyclic ring system of 5 to 12 ring atoms, comprising 1, 2, 3 or 4 heteroatoms selected from N, O and S, the remaining ring atoms being carbon. Examples of heteroaryl moieties include pyrrolyl, furanyl, thienyl, imidazolyl, oxazolyl, thiazolyl, triazolyl, oxadiazolyl, thiadiazolyl, tetrazolyl, pyridinyl, pyrazinyl, pyrazolyl, pyridazinyl, pyrimidinyl, triazinyl, azepinyl, diazepinyl, isoxazolyl, benzofuranyl, isothiazolyl, benzothienyl, indolyl, isoindolyl, isobenzofuranyl, benzimidazolyl, benzoxazolyl, benzoisoxazolyl, benzothiazolyl, benzoisothiazolyl, benzooxadiazolyl, benzothiadiazolyl, benzotriazolyl, purinyl, quinolinyl, isoquinolinyl, quinazolinyl, or quinoxalinyl.

(27) The term “heterocycloalkyl” denotes a monovalent saturated or partly unsaturated mono- or bicyclic ring system of 3 to 12 ring atoms, comprising 1, 2, or 3 ring heteroatoms selected from N, O and S, the remaining ring atoms being carbon. In particular embodiments, heterocycloalkyl is a monovalent saturated monocyclic ring system of 4 to 7 ring atoms, comprising 1, 2, or 3 ring heteroatoms selected from N, O and S, the remaining ring atoms being carbon. In particular embodiments, heterocycloalkyl is a benzo-fused heterocyclic group of 9-12 ring atoms. Examples are benzo[d][1,3]dioxolyl, 2,3-dihydrobenzo[b][1,4]dioxinyl, 3,4-dihydro-2H-benzo[b][1,4]oxazinyl. Examples for monocyclic saturated heterocycloalkyl are aziridinyl, oxiranyl, azetidinyl, oxetanyl, pyrrolidinyl, tetrahydrofuranyl, tetrahydro-thienyl, pyrazolidinyl, imidazolidinyl, oxazolidinyl, isoxazolidinyl, thiazolidinyl, piperidinyl, tetrahydropyranyl, tetrahydrothiopyranyl, piperazinyl, morpholinyl, thiomorpholinyl, 1,1-dioxo-thiomorpholin-4-yl, azepanyl, diazepanyl, homopiperazinyl, or oxazepanyl. Examples for bicyclic saturated heterocycloalkyl are 8-aza-bicyclo[3.2.1]octyl, quinuclidinyl, 8-oxa-3-aza-bicyclo[3.2.1]octyl, 9-aza-bicyclo[3.3.1]nonyl, 3-oxa-9-aza-bicyclo[3.3.1]nonyl, or 3-thia-9-azabicyclo[3.3.1]nonyl. Examples for partly unsaturated heterocycloalkyl are dihydrofuryl, imidazolinyl, dihydro-oxazolyl, tetrahydro-pyridinyl, or dihydropyranyl.

(28) The term “hydroxyalkyl” denotes an alkyl group wherein at least one of the hydrogen atoms of the alkyl group has been replaced by a hydroxy group. Examples of hydroxyalkyl include hydroxymethyl, 2-hydroxyethyl, 2-hydroxypropyl, 3-hydroxypropyl, 1-(hydroxymethyl)-2-methylpropyl, 2-hydroxybutyl, 3-hydroxybutyl, 4-hydroxybutyl, 2,3-dihydroxypropyl, 2-hydroxy-1-hydroxymethylethyl, 2,3-dihydroxybutyl, 3,4-dihydroxybutyl or 2-(hydroxymethyl)-3-hydroxypropyl.

(29) The term “alkoxyalkyl” denotes an alkyl group wherein at least one of the hydrogen atoms of the alkyl group has been replaced by an alkoxy group. Exemplary alkoxyalkyl groups include 2-methoxyethyl, 3-methoxypropyl, 1-methyl-2-methoxyethyl, 1-(2-methoxyethyl)-3-methoxypropyl, and 1-(2-methoxyethyl)-3-methoxypropyl.

(30) The term “half maximal inhibitory concentration” (IC50) denotes the concentration of a particular compound required for obtaining 50% inhibition of a biological process in vitro.

(31) IC50 values can be converted logarithmically to pIC50 values (−log IC50), in which higher values indicate exponentially greater potency. The IC50 value is not an absolute value but depends on experimental conditions e.g. concentrations employed. The IC50 value can be converted to an absolute inhibition constant (Ki) using the Cheng-Prusoff equation (Biochem. Pharmacol. (1973) 22:3099).

(32) The term “subject” denotes a vertebrate. In certain embodiments, the vertebrate is a mammal. Mammals include humans, non-human primates such as chimpanzees and other apes and monkey species, farm animals such as cattle, horses, sheep, goats, and swine, domestic animals such as rabbits, dogs, and cats, laboratory animals including rodents, such as rats, mice, and guinea pigs. In certain embodiments, a mammal is a human. The term subject does not denote a particular age or sex.

(33) The term “pharmaceutically acceptable salts” denotes salts which are not biologically or otherwise undesirable. Pharmaceutically acceptable salts include both acid and base addition salts.

(34) The terms “pharmaceutically acceptable excipient” and “therapeutically inert excipient” can be used interchangeably and denote any pharmaceutically acceptable ingredient in a pharmaceutical composition having no therapeutic activity and being non-toxic to the subject administered, such as disintegrators, binders, fillers, solvents, buffers, tonicity agents, stabilizers, antioxidants, surfactants, carriers, diluents or lubricants used in formulating pharmaceutical products.

(35) The present invention relates to radiolabeled compounds of formula I

(36) ##STR00003##

(37) wherein

(38) A is heterocycloalkyl,

(39) B is aryl or heteroaryl both optionally substituted by C.sub.1-7alkyl or halogen,

(40) R.sub.1 is selected from aryl, heteroaryl optionally substituted by C.sub.1-7alkyl, C.sub.1-7alkoxy, cyano, halogen, —C(O)O—C.sub.1-7alkyl, —N(C.sub.1-7alkyl).sub.2, halo-C.sub.1-7alkoxy, —SO.sub.2—C.sub.1-7alkyl, C.sub.2-7alkynyl, R.sub.2 is selected from aryl, heteroaryl optionally substituted by halogen, C.sub.1-7alkoxy, halo-C.sub.1-7alkoxy, hydroxyl, —N(C.sub.1-7alkyl).sub.2, halo-C.sub.1-7alkoxy-(C.sub.1-7-alkoxy).sub.n, hydroxyl-halo-C.sub.1-7alkoxy, hydroxyl-(C.sub.1-7alkoxy), cyano, C.sub.1-7alkyl, C.sub.2-7alkynoxy, C.sub.2-7alkynoxy-(C.sub.1-7-alkoxy).sub.n, halo-C.sub.1-7 alkoxy substituted by —O—Si(C.sub.1-7alky).sub.2-C.sub.1-7alkyl and heterocycloalkyl optionally substituted by C.sub.1-7alkyl,

(41) n is 1, 2

(42) wherein either A, B, R.sub.1, R.sub.2, is labeled with a radionuclide selected from .sup.3H, .sup.11C or .sup.18F.

(43) In a particular embodiment, the invention relates to compounds of formula I, wherein

(44) A is heterocycloalkyl,

(45) B is aryl or heteroaryl both optionally substituted by C.sub.1-7alkyl or halogen,

(46) R.sub.1 is selected from aryl, heteroaryl optionally substituted by C.sub.1-7alkyl, C.sub.1-7alkoxy, cyano, halogen, C(O)O—C.sub.1-7alkyl, —N(C.sub.1-7alkyl).sub.2, halo-C.sub.1-7alkoxy, —SO.sub.2—C.sub.1-7alkyl and

(47) R.sub.2 is selected from aryl, heteroaryl optionally substituted by halogen, C.sub.1-7alkoxy, halo-C.sub.1-7alkoxy, hydroxyl, —N(C.sub.1-7alkyl).sub.2, halo-C.sub.1-7alkoxy-(C.sub.1-7-alkoxy).sub.n, C.sub.1-7alky-Si—O-halo-C.sub.1-7 alkoxy, hydroxyl-halo-C.sub.1-7alkoxy, hydroxyl-(C.sub.1-7alkoxy), cyano, C.sub.1-7alkyl, heterocycloalkyl optionally substituted by C.sub.1-7alkyl.

(48) In a particular embodiment, the invention relates to radiolabeled compounds of formula I, wherein A is selected from piperazinyl and hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl.

(49) In a particular embodiment, the invention relates to radiolabeled compounds of formula I, wherein B is selected from a 5- or 6-membered aryl or a 5- or 6-membered heteroaryl, preferably selected from phenyl, pyridinyl, piperazinyl, pyrimidinyl, pyrazinyl.

(50) In a particular embodiment, the invention relates to radiolabeled compounds of formula I, wherein A is piperazinyl and B is phenyl.

(51) In a particular embodiment, the invention relates to radiolabeled compounds of formula I, wherein A is piperazinyl and B is pyridinyl.

(52) In a particular embodiment, the invention relates to radiolabeled compounds of formula I, wherein R.sub.2 is selected from a 5- or 6-membered aryl or 5- or 6-membered heteroaryl group.

(53) In a particular embodiment, the invention relates to radiolabeled compounds of formula I, wherein R.sub.2 is selected from phenyl, pyridinyl.

(54) In a particular embodiment, the invention relates to radiolabeled compounds of formula I, wherein R.sub.2 is substituted by halogen, C.sub.1-7alkoxy, hydroxyl, 6-membered heterocycloalkyl, C.sub.1-7alkyl, halo-C.sub.1-7alkoxy, halo-C.sub.1-7alkoxy-(C.sub.1-7-alkoxy).sub.n where n is 1, 2.

(55) In a particular embodiment, the invention relates to radiolabeled compounds of formula I, wherein R.sub.2 is labeled with a radionuclide selected from .sup.3H, .sup.18F and .sup.11C.

(56) In a particular embodiment, the invention relates to radiolabeled compounds of formula I selected from the group consisting of.

(57) ##STR00004## ##STR00005##

(58) In another embodiment the present invention relates to the use of the radiolabeled compounds of the present invention in an alpha synuclein and/or Abeta binding study.

(59) In another embodiment the present invention relates to the use of the radiolabeled compounds of the present invention in diagnostic imaging of alpha synuclein and/or Abeta aggregates in the brain of a mammal.

(60) In another embodiment, the present invention relates to a pharmaceutical composition comprising a radiolabeled compound of the present invention and a pharmaceutical acceptable carrier.

(61) In a further embodiment, the present invention relates to a method of imaging alpha synuclein and/or Abeta deposits in a mammal, comprising:

(62) introducing into a mammal a detectable quantity of a pharmaceutical composition of the present invention; and

(63) detecting the compound associated with alpha synuclein and/or Abeta deposits.

(64) In another embodiment, the present invention relates a use of a compound of the present invention for diagnostic imaging of alpha synuclein and/or Abeta deposits in the brain of a mammal.

(65) The preparation of compounds of formula (I) of the present disclosure may be carried out in sequential or convergent synthetic routes. Syntheses of the disclosure are shown in the following general schemes. The skills required for carrying out the reactions and purifications of the resulting products are known to those persons skilled in the art. In case a mixture of enantiomers or diastereoisomers is produced during a reaction, these enantiomers or diastereoisomers can be separated by methods described herein or known to the man skilled in the art such as e.g. (chiral) chromatography or crystallization. The substituents and indices used in the following description of the processes have the significance given herein.

(66) Methods to Prepare Compounds of General Structure (A1) are Illustrated in Scheme 1.

(67) Compounds of general structure (A1) can be prepared from intermediates of structure (B) by reacting the amino group of (B) with carboxylic acids of general structure R.sub.2COOH in the presence of amide coupling reagents such as HATU, EDC.HCl/HOBt or T3P. A base such as DIPEA or Et.sub.3N might be added and the reaction can be performed in solvents such as DMF or THF. Alternatively, compounds of structure (A1) can be prepared by reacting (B) with an acid chloride of general structure R.sub.2COCl, in the presence of a base such as DIPEA or Et.sub.3N in a solvent such as DCM. Intermediates (B) can be prepared in two steps from piperazines of general structure (C) and nitro compounds (D). In a first step the piperazines (C) are reacted with nitro compounds (D) under nucleophilic aromatic substitution conditions to obtain intermediates (E). These for instance make use of a base such as K.sub.2CO.sub.3 or DIPEA in solvents such as DMSO, DMF or NMP. Reduction of nitro intermediates (E) to compounds (B) can be achieved by various reaction conditions, including but not limited to the use of H.sub.2 in the presence of Pd/C in a solvent such as EtOH, or the use of hydrazine monohydrate with Raney Ni in a solvent such as EtOH or a solvent mixture consisting of EtOH/THF, or the use of SnCl.sub.2.2H.sub.2O in EtOH or under Béchamp reduction conditions.

(68) When intermediates of general structure (B) contain a pyridazine ring, the compounds can be prepared in one step starting from piperazines of structure (C) and 6-iodopyridazin-3-amine. This reaction can be catalyzed by using CuI in the presence of L-hydroxyproline and a base such as K.sub.3PO.sub.4 in a solvent such as DMSO.

(69) When intermediates of general structure (B) contain a pyrazine ring, the compounds can be prepared in three steps from 2,5-dichloropyrazine. For instance, reaction of 2,5-dichloropyrazine with 1-(2-pyridyl)piperazine in the presence of a base such as Cs.sub.2CO.sub.3 in a solvent as for example DMF leads to 2-chloro-5-[4-(2-pyridyl)piperazin-1-yl]pyrazine. Reaction of this compound with HNCPh.sub.2 in presence of a catalyst system such as [Pd.sub.2(dba).sub.3], BINAP, NaOtBu in Tol followed by deprotection of the amino group, for instance with HONH.sub.2.Math.HCl, NaOAc.Math.3H.sub.2O in MeOH, leads to a pyrazine of general structure (B).

(70) ##STR00006##

(71) When compounds of general structure (A1) contain an R.sub.2 consisting of a phenol substituent, as for example structure (A2) in Scheme 2, the compounds can be prepared in one step starting from an acetic acid ester of general structure (F) by saponification of the ester bond. A wide range of other ester groups might be used. Saponification of the ester can be achieved for example using aqueous NaOH in a solvent such as MeOH. Compounds of general structure (F) can be prepared according to the methods described in Scheme 1 above.

(72) Phenols of structure (A2) can be further elaborated by alkylation to obtain for example compounds of general structure (A3). This can be for instance achieved by reaction with an alkylating reagent such as TsO(CH.sub.2).sub.2O(CH.sub.2).sub.2OH in presence of a base as Cs.sub.2CO.sub.3 in a solvent as DMF.

(73) ##STR00007##

(74) In a certain embodiment of this invention the reagent R.sub.2COOH used in Scheme 1 consists of 4-[2-(2-fluoroethoxy)ethoxy]benzoic acid (K) (Scheme 3). Compound (K) can be prepared in four steps by first introducing one tosyl group onto diethyleneglycol (G), for instance by reaction with TsCl, Ag.sub.2O and KI in DCM at 0° C. Fluorination of (H) can be performed for example with DAST in DCM to obtain (I). Intermediate (I) is used to alkylate 4-hydroxybenzoic acid methyl esther in the presence of a base such as Cs.sub.2CO.sub.3 in a solvent as DMF. The resulting compound (J) is then transformed to (K) by saponification of the ester, for instance using aqueous NaOH in MeOH.

(75) ##STR00008##

(76) In a further embodiment of this invention, the compounds possess the general structures (A4) or (A5) as depicted in Scheme 4. Compounds of general structure (A4) can be prepared for instance by reaction of an aniline of general structure (B2) (prepared as described in Scheme 1) with a reagent obtained by the reaction of an ester such as (N) with Me.sub.3Al in a solvent such as dioxane. Compound (N) can be prepared starting from epoxide (L) by reaction with a fluoride source such as TBAF in a solvent such as Tol, leading to intermediate (M). Alcohol (M) can be transformed into silyl ether (N) for instance by the use of TBDM-SCl, imidazole and DMAP in DCM.

(77) Further elaboration of general structures (A4) by removing the silicon protecting group with a reagent such as TBAF in a solvent as for example THF leads to compounds of general structure (A5).

(78) ##STR00009##

(79) In a further embodiment of this invention the reagent R.sub.2COCl used in Scheme 1 consists of 4-(fluoromethoxy)benzoyl chloride (Q) (Scheme 5). Compound (Q) can be prepared from ester (0) by saponicfication to (P) with, for instance, aqueous NaOH in a mixture of THF/EtOH followed by chlorination, for example using oxalyl chloride in the presence of DMF in a solvent as DCM.

(80) ##STR00010##

(81) In a certain embodiment of this invention, the compounds are 4-methoybenzamides of general structure (A6) (Scheme 6). Such compounds can be prepared according to the methods illustrated in Scheme 1 or alternatively starting from 4-methoxybenzoyl chloride. Reaction of 4-methoxy benzoyl chloride with 4-bromoaniline in the presence of a base as DIPEA in a solvent as DCM leads to intermediate (R). Reaction of (R) with 1-Cbz-piperazine under Buchwald cross coupling conditions, using for instance [Pd.sub.2(dba).sub.3], XPhos and tBuONa in dioxane gives intermediate (S). Deprotection of the amine group can be achieved under reducing conditions, such as for example the use of 1-methyl-1,4-cyclohexadiene and Pd/C in EtOH. This yields intermediate (T) that can be derivatized into a range of final compounds of general structure (A6) by aromatic nucleophilic substitution of aryls of general structure R.sub.1Br in the presence of a base such as DIPEA in a solvent as NMP.

(82) ##STR00011##

(83) Scheme 7 illustrates a further method for preparing compounds of the type (A1) with the particular structure (A7). In this embodiment of the invention, the synthesis starts from 1-(4-nitrophenyl)piperazine (U) that is reacted with aryl bromides of structure R.sub.1Br under Buchwald cross coupling conditions. This transformation can for instance be performed using [Pd(OAc).sub.2], RuPhos and Cs.sub.2CO.sub.3 in dioxane. The following reduction and amide bond formation steps can be performed using one of the several methods described above. For example, use of Fe and NH.sub.4Cl in EtOH/H.sub.2O reduces compounds of general structure (V) to anilines of the type (B2). Such anilines lead to the final products (A7) by reaction with R.sub.2COOH, HATU and DIPEA in DMF.

(84) ##STR00012##

(85) In a certain embodiment of this invention, the compounds possess the structure (AC) or (AH) (Scheme 8). Such compounds can be prepared from a common intermediate (W) (WO2014/139978 A1, WO2015/144605 A1). Preparation of the (S,S)-enantiomer (AC) can be performed starting by reaction of (W) with 2-chloropyridine under nucleophilic aromatic substitution conditions, as for example heating in the presence of Et.sub.3N in a solvent as DMA or NMP. The thus obtained intermediate (X) is then transformed in the corresponding amine (Y) by Boc deprotection. Several conditions can be used for this step, as for example reaction with TFA in DCM. Transformation of intermediate (Y) to the final compound (AC) can be achieved in analogy to the several methods described above. For instance reaction of (Y) with 4-fluoronitrobenzene and K.sub.2CO.sub.3 in DMSO at 90° C. yields (Z). Reduction of nitro compound (Z) to aniline (AB) can be performed for example with H.sub.2, Pd/C and AcOH in EtOH. (AB) can then be subjected to amide coupling conditions to get to compound (AC), for example by reaction with Me.sub.3Al and 4-methoxybenzoic acid methyl ester in dioxane. Preparation of the (R,R)-enantiomer (AH) can be achieved by reacting intermediate (W) with 4-fluoronitrobenzene and K.sub.2CO.sub.3 in DMSO to yield (AD). Removal of the Boc protecting group from (AD) can be achieved for example with TFA in DCM. The so obtained amine intermediate (AE) can further be elaborated into compound (AF) by reaction with 2-chloropyridine and Et.sub.3N in DMA or NMP by heating. Nitro intermediate (AF) can be reduced to aniline (AG) using several of the conditions described above, as for example H.sub.2, Pd/C and AcOH in EtOH. Aniline (AG) can finally be transformed in the desired product (AH) using amide coupling conditions, as for instance reaction with 4-methoxybenzoic acid, HATU and DIPEA in DMF.

(86) ##STR00013##

(87) Compounds of the present invention can be labeled with tritium using a range of different methods. Scheme 9 illustrates two approaches. In the first approach, a compound of general structure (AI) or (AJ) is tritiated by direct isotope exchange reaction catalyzed by Crabtree's or Kerr's catalyst under an atmosphere of [.sup.3H]H.sub.2, in a solvent such as DMF, DCM or chlorobenzene. Compounds of general structure (AJ) possessing a 2-piridyl substituent in position R.sub.1 typically lead to higher incorporation of tritium and thus higher specific activities.

(88) Alternatively, when the compounds possess a methoxy group like in the general structure (AL), labelling can be achieved by alkylation of a phenolic precursor (AK) using a reagent such as [.sup.3H]methylnosylate in presence of a base as for example Cs.sub.2CO.sub.3 in solvents as THF or DMSO.

(89) ##STR00014##

(90) Materials and Methods

(91) Human Tissue Samples

(92) Human PD brain tissue blocks were obtained from the Banner Sun Health Research Institute (Sun City, Ariz., USA). Pathological diagnosis of PD was made according to standard criteria based on neuropathological data.

(93) Animals

(94) The transgenic mouse strain A30P carries a mutant form of the human aSyn gene which is associated with the development of a familial form of PD. The mouse line B6.D2-Tg(Thyl-SNCA*30P)31Pjk was generated in-house and animals were used for this study at the onset of hind limb mobility problems and a resting tremor phenotype which typically occurred at an age of 12-16 months.

(95) Radioligands

(96) The screening radioligand [.sup.3H]Example-3, [.sup.3H]Example-12, [.sup.3H]Example-121, [.sup.3H]Example-122, [.sup.3H]Example-134, [.sup.3H]Example-135 and [.sup.3H]Example-136 were synthesized in-house (specific activity 77 Ci/mmol, radiochemical purity 99.5%). All other [.sup.3H]radioligands were also tritiated at Roche with a specific activity of >71 Ci/mmol. Radiochemical purity was >95% for all ligands.

(97) Autoradiography

(98) Ten μm thick A30P transgenic mouse brain sections and human PD brain sections are generated with a cryostat (Leica CM3050) at −17° C. chamber temperature and −15° C. object temperature. Sections are transferred to Histobond+ microscope slides (Marienfeld Laboratory Glasware). After drying for 3 hours at room temperature the sections are stored at −20° C. The sections are incubated with the radioligand (0.3-30 nM) and the respective cold compound (at various concentrations) in 50 mM Tris buffer, pH 7.4 at room temperature for 30 min. After washing 3×10 min at 4° C. in 50 mM Tris buffer, pH 7.4 and 3 quick dips in H.sub.2O dist. at 4° C. the sections are dried at 4° C. for 3 h. The sections are placed in a FujiFilm Cassette, exposed to an Imaging Plate (BAS-IP TR 2025) for five days and afterwards scanned with a FujiFilm IP reader (BAS-5000) with a resolution of 25 μM per pixel.

(99) Data Analysis

(100) The signal intensity (Dens—PSL/mm2) in the region of interest (ROI) of the autoradiogram is quantified with the software MCID analysis (version 7.0, Imaging Research Inc.). The specific binding (SB) of radioligand [.sup.3H]Example-3 binding was calculated by subtracting non-specific binding (NSB) in midbrain and pons determined in presence of 3 μM cold EXAMPLE 3 from the total binding (TB) in midbrain and pons which was obtained with radioligand only. The % displacement by various compounds was calculated as following: % displacement=100−(SBcompound/SBEXAMPLE 3 only)*100.

(101) Immunohistochemistry

(102) Antibody staining of sections is performed after exposure and scanning of the tissue sections undergoing classical autoradiographical analysis. Brain sections were hydrated in PBS and blocked in 1% bovine serum albumin, 1% ovalbumin and 1% normal goat serum in PSB for 20 min. This is followed by overnight incubation at 4° C. with a mixture of anti-aSyn pS129 monoclonal antibody (generated in-house; 1 μg/mL) in blocking buffer. After washing with PBS+0.01% Tween20 and incubation with a fluorescent dye-labeled secondary antibody autofluorescence of lipofuscin is reduced by quenching through incubation in 0.3% Sudan Black in 70% EtOH for 3 min. After rinsing the slides in 70% EtOH and two times in H.sub.2O dist., slides are embedded with Aquapolymount mounting medium, dried for at least 3 h at RT and scanned with the MetaSystem Metafer image analysis system (or Pannoramic p250).

(103) Ex Vivo Autoradiography

(104) Radiotracers are intravenously injected in A30P mice (1 mCi/kg) to analyze penetration through the blood-brain barrier and target-related retention in aSyn expressing brain regions. Animals are sacrificed at 15 or 30 min after tracer administration, brains are sampled and frozen. Brain sections are generated with a cryostat (Leica CM3050) at −17° C. chamber temperature and −15° C. object temperature and sections are exposed to an Imaging Plate (BAS-IP TR 2025) for five days and afterwards scanned with a FujiFilm IP reader (BAS-5000) with a resolution of 25 μM per pixel.

(105) Results

(106) aSyn In Vitro Binding Assay

(107) This in vitro binding assay assesses the affinity of compounds for native aSyn aggregates in tissue sections by autoradiography. The tritiated compounds are incubated in vitro with tissue sections from A30P transgenic mouse brains and human PD brain tissue. [.sup.3H]Example-3 shows strong binding to aSyn aggregates in A30P transgenic mouse brain tissue with histologically confirmed high aSyn load in midbrain and pons using the aSyn-specific antibody pS129 (FIG. 1, right image). Radioligand binding and antibody staining show excellent co-localization with strong signals in midbrain, pons and subthalamic regions and weaker signals in cortical areas. Human brain tissue samples from PD patients are characterized by a much lower density of aSyn aggregates compared to the overexpressing transgenic mouse model A30P. As a consequence, macroscopic co-localization of radioligand binding and aSyn mAb signals on human PD tissue sections is challenging (FIG. 1, middle image) but can be clearly demonstrated at higher magnification (FIG. 1, right image). The hot spots of the autoradiograms show good co-localization with LBs stained by the aSyn mAb pS129.

(108) ASyn In Vitro Displacement Assay

(109) This in vitro displacement binding assay assesses the affinity of novel compounds for native aSyn aggregates. The compounds are co-incubated with the screening radioligand [.sup.3H]Example-3 and the compound's displacement potency of [.sup.3H]Example-3 binding is determined by in vitro autoradiography using A30P transgenic mouse brain sections (FIG. 2). Total binding (TB) is determined at 3 nM [.sup.3H]Example-3 while non-specific binding (NSB) is determined by co-incubation with 3 μM unlabeled Example-3. The NSB level is defined as 100% displacement. Several high-affinity displacers are identified (FIG. 3) and selected for tritiation and a direct binding test using autoradiography (FIG. 4).

(110) In Vivo Binding/Ex Vivo Autoradiography

(111) Upon intravenous administration in A30P mice, all radiotracers reveal good penetration through the blood-brain barrier and a clear target-related retention in midbrain, pons and subthalamic regions as visualized by ex vivo autoradiography (FIG. 5). No significant off-target binding is observed in brain regions devoid of aSyn pathology.

(112) Aβ In Vitro Displacement Assay

(113) This in vitro displacement binding assay assesses the affinity of novel compounds for native Aβ aggregates in human AD brain tissue samples. The compounds are co-incubated with the screening radioligand [.sup.3H]Example 3 and the compound's displacement potency of [.sup.3H]Example 3 binding is determined by in vitro autoradiography using AD brain tissue sections (FIG. 6). TB is determined at 3 nM [.sup.3H]Example 3 while NSB is determined by co-incubation with 3 μM unlabeled Example 3. The NSB level is defined as 100% displacement.

(114) Aβ In Vitro Binding Assay

(115) This direct in vitro binding assay assesses the affinity of radiotracers for native Aβ aggregates in tissue sections by autoradiography. The tritiated compounds are incubated in vitro with sections from human AD brain samples and show strong binding to Aβ aggregates (FIG. 7). Radioligand binding and Aβ mAb staining show excellent co-localization as exemplified for [.sup.3H]Example-134 (FIG. 8). The hot spots of the autoradiograms show good co-localization with Aβ plaques stained by the Aβ mAb MOAB-2.

EXAMPLES

Example 1

2-Fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(116) ##STR00015##

a) 1-(4-Nitrophenyl)-4-(pyridin-2-yl)piperazine

(117) ##STR00016##

(118) 1-(Pyridin-2-yl)piperazine (4.90 g, 30 mmol) was dissolved at 22° C. in DMSO (10 ml) under an inert atmosphere. K.sub.2CO.sub.3 (6.22 g, 45 mmol) was added at 22° C. followed by 1-fluoro-4-nitrobenzene (4.66 g, 3.5 ml, 33 mmol). The reaction mixture was heated to 90° C. and stirred at this temperature for 90 min. The mixture was diluted with H.sub.2O (150 ml) and extracted with DCM (3×150 ml). The organic layers were washed with sat. aq. NaCl (1×150 ml), dried over MgSO.sub.4 (35 g), filtered over a glass-frit and washed with DCM (2×100 ml). The filtrate was evaporated at 40° C. and finally dried in HV to mainly remove DMSO. The residue (9.18 g) was partially dissolved in DCM/MeOH 1:1 (60 ml), adsorbed on 32 g Isolute HM-N 9800, evaporated and then purified by flash chromatography (silica gel, 330 g; MeOH in DCM 0% to 5%). Pure fractions corresponding to the product were collected to give after evaporation at 40° C. the title compound (6.89 g, 81%) as an orange solid. LC-MS: m/z=285.1 [M+H].sup.+.

b) 4-(4-(Pyridin-2-yl)piperazin-1-yl)aniline

(119) ##STR00017##

(120) 1-(4-Nitrophenyl)-4-(pyridin-2-yl)piperazine (6.77 g, 23.8 mmol) was suspended in EtOH (290 ml) and placed under inert atmosphere at 22° C. and a slurry of Pd/C 10% (2.53 g, 2.38 mmol) in EtOH (50 ml) was added. The reaction vessel was again inerted, then set under H.sub.2 and reacted at 22° C. for 15 h. The catalyst was filtered over a membrane filter, washed with EtOH (2×50 ml) and the filtrate was evaporated. The residue was dissolved in DCM/MeOH 1:1 (20 ml), adsorbed on 12.5 g Isolute HM-N 9800, evaporated and then purified by flash chromatography (silica gel, 330 g, MeOH in DCM 1% to 5%). Fractions containing pure product were collected to give after evaporation at 40° C. the title compound (5.02 g, 83%) as a light yellow solid. LC-MS: m/z=255.2 [M+H].sup.+.

c) 2-Fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(121) 2-Fluoro-4-methoxybenzoic acid (854 mg, 5.02 mmol) was dissolved in DMF (15 ml) to give a light yellow solution. DIPEA (1.18 g, 1.59 ml, 9.12 mmol) and HATU (2.08 g, 5.47 mmol) were added, and the reaction mixture was stirred at rt for 30 min. Then 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (1.16 g, 4.56 mmol) was added and the reaction mixture was stirred at rt for 1 h. H.sub.2O was added and the product was extracted three times with DCM. The combined organic layers were dried over Na.sub.2SO.sub.4, filtered and evaporated. The crude material was suspended in DCM and filtered to provide 1.29 g (70%) of the title compound as a light grey solid. LC-MS m/z=407.2 [M+H].sup.+.

Example 2

4-Hydroxy-N-[4-[4-(2-pyridyl)piperazin-1-yl]phenyl]benzamide

(122) ##STR00018##

a) [4-[[4-[4-(2-Pyridyl)piperazin-1-yl]phenyl]carbamoyl]phenyl] acetate

(123) ##STR00019##

(124) 4-Acetoxybenzoic acid (1.59 g, 8.8 mmol) was dissolved at 22° C. in DCM (65 ml) under an inert atmosphere. Oxalyl chloride (1.68 g, 1.16 ml, 13.2 mmol) was added at 22° C. followed by DMF (32.2 mg, 34.1 μl, 440 μmol) and the reaction mixture was stirred at 22° C. for 2 h. The mixture was evaporated at 40° C. and the resulting acid chloride was dissolved in DCM (32.3 ml) and added dropwise (5 min) at 22° C. to a solution of 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (2.24 g, 8.8 mmol) and DIPEA (4.55 g, 6.15 ml, 35.2 mmol) in DCM (80 ml) keeping the internal temperature below 20° C. (ice-bath). Stirring was continued at 22° C. for 30 min. The reaction was stopped by adding at 22° C. MeOH (5.64 g, 7.12 ml, 176 mmol). Stirring was continued for 1 h before filtering through a membrane-filter. Solids were washed with DCM (2×35 ml) and the cake was dried for 2 min (air dried by suction). Then the cake was washed with H.sub.2O (2×35 ml) and dried in HV to give the title compound (3.20 g, 87%) as white solid. LC-MS: m/z=417.3 [M+H].sup.+.

b) 4-Hydroxy-N-[4-[4-(2-pyridyl)piperazin-1-yl]phenyl]benzamide

(125) 4-((4-(4-(Pyridin-2-yl)piperazin-1-yl)phenyl)carbamoyl)phenyl acetate (3.06 g, 7.34 mmol) was suspended in MeOH (100 ml) under inert atmosphere at 22° C. NaOH (1 M aq., 29.4 ml, 29.4 mmol) was added. The mixture was stirred at 22° C. for 6 h to give a clear solution. The solution was treated with HCl (1 M aq., 29.4 ml, 29.4 mmol) leading to precipitation of the product. The mixture was stirred for an additional 60 min, filtered over a glass frit, washed with H.sub.2O/MeOH 1:1 (1×60 ml), H.sub.2O (2×60 ml) and dried under HV to give the title compound (2.57 g, 94%) as white solid. LC-MS: m/z=375.3 [M+H].sup.+.

Example 3

4-Methoxy-N-[4-(4-pyridin-2-ylpiperazin-1-yl)phenyl]benzamide

(126) ##STR00020##

(127) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (500 mg, 1.97 mmol) and 4-methoxybenzoic acid (329 mg, 2.16 mmol). Yield 474 mg (61%). Off-white solid. LC-MS: m/z=389.2 [M+H].sup.+.

Example 4

6-Methoxy-N-[4-[4-(5-methyl-2-pyridyl)piperazin-1-yl]phenyl]pyridine-3-carboxamide

(128) ##STR00021##

a) 1-(5-Methylpyridin-2-yl)-4-(4-nitrophenyl)piperazine

(129) ##STR00022##

(130) 1-(5-Methylpyridin-2-yl)piperazine (3.1 g, 17.5 mmol), 1-chloro-4-nitrobenzene (3.84 g, 24 mmol) and DIPEA (4.6 ml, 3.38 g 26 mmol) were combined at room temperature in NMP (3 ml) then stirred and heated to 125° C. for 4.5 h. The cooled mixture was partitioned between NaHCO.sub.3 and EtOAc and extracted with EtOAc (3×). The combined organic phases were then washed with H.sub.2O and concentrated onto silica. The crude solid was dry-loaded onto a silica column and purified by flash column chromatography eluting with DCM to DCM/EtOAc 1:1 to afford the title compound 2.7 g (52%). This material was used in the following step with no further characterization.

b) 4-(4-(5-Methylpyridin-2-yl)piperazin-1-yl)aniline

(131) ##STR00023##

(132) 1-(5-Methylpyridin-2-yl)-4-(4-nitrophenyl)piperazine (2.7 g, 9.05 mmol), iron powder (2.3 g, 41 mmol), acetic acid (5 ml) and H.sub.2O (5 ml) were combined and refluxed for 2 h. Then another portion of iron powder (2.3 g, 41 mmol) and acetic acid (5 ml) were added and the mixture was stirred and heated for another 2 h. The mixture was cooled, filtered and concentrated and the residue partitioned between NaHCO.sub.3 and DCM and extracted into DCM (3×). The combined organic phases were washed with H.sub.2O and dried and evaporated onto silica. The crude solid adsorbed onto silica was dry-loaded onto a silica column and purified by flash column chromatography eluting with isohexane 100% to EtOAc 100% to MeOH 50%. The product was obtained as a beige solid 1.89 g (78%).

(133) .sup.1H NMR (400 MHz, CDCl.sub.3): δ 8.04 (d, J=2.0 Hz, 1H), 7.33 (dd, J=2.3, 8.4 Hz, 1H), 6.88-6.85 (m, 2H), 6.68-6.62 (m, 3H), 3.64-3.60 (m, 4H), 3.16-3.13 (m, 4H), 2.21 (s, 3H).

c) 6-Methoxy-N-(4-(4-(6-methylpyridin-3-yl)piperazin-1-yl)phenyl)nicotinamide

(134) ##STR00024##

(135) This compound was synthesized following the general procedure B.

(136) Yield: 120 mg.

(137) .sup.1H NMR (400 MHz, CDCl.sub.3) δ 8.68 (d, J=2.3 Hz, 1H), 8.10-8.05 (m, 2H), 7.58 (s, 1H), 7.52 (d, J=8.8 Hz, 2H), 7.35 (dd, J=2.3, 8.4 Hz, 1H), 7.01-6.97 (m, 2H), 6.83 (d, J=8.7 Hz, 1H), 6.66 (d, J=8.7 Hz, 1H), 4.00 (s, 3H), 3.67-3.63 (m, 4H), 3.31-3.27 (m, 4H), 2.22 (s, 3H). LC-MS: Rt=2.59 min, m/z=404, [M+H].sup.+.

Example 5

4-Methyl-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(138) ##STR00025##

(139) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (100 mg, 393 μmol) and 4-methylbenzoic acid (58.9 mg, 433 μmol). Yield 96 mg (66%). White solid. LC-MS: m/z=373.2 [M+H].sup.+.

Example 6

4-(4-Methylpiperazin-1-yl)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(140) ##STR00026##

(141) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (100 mg, 393 μmol) and 4-(4-methylpiperazin-1-yl)benzoic acid (95.3 mg, 433 μmol). Yield 38 mg (21%). Off-white solid. LC-MS: m/z=229.2 [M+2H].sup.2+.

Example 7

4-(Dimethylamino)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(142) ##STR00027##

(143) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (70 mg, 275 μmol) and 4-(dimethylamino)benzoic acid (50 mg, 303 μmol). Yield 27 mg (24%). Off-white solid. LC-MS: m/z=201.7 [M+2H].sup.2+.

Example 8

4-Morpholino-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(144) ##STR00028##

(145) 4-Morpholinobenzoic acid (122 mg, 590 μmol) was dissolved in DMF (5 ml). 4-(4-(Pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (100 mg, 393 μmol), HOBt (117 mg, 865 μmol), EDCl (188 mg, 983 μmol) and Et.sub.3N (39.8 mg, 54.5 μl, 393 μmol) were added and the reaction mixture was stirred at rt for 7 h. Then additional 30 mg of 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) were added and the mixture was stirred for 16.5 h. H.sub.2O was added and the product was extracted with DCM (3×). The combined organic layers were dried over Na.sub.2SO.sub.4 and evaporated. The crude material was suspended in DCM and filtered to provide 25 mg (14%) of the title compound as an off-white solid. LC-MS: m/z=222.7 [M+2H].sup.2+.

Example 9

2-Fluoro-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(146) ##STR00029##

(147) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (100 mg, 393 μmol) and 2-fluorobenzoic acid (60.6 mg, 433 μmol). The product was purified with preparative HPLC to yield 78 mg (53%) of the title compound as a white solid. LC-MS: m/z=377.2 [M+H].sup.+.

Example 10

2-Fluoro-4-methyl-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(148) ##STR00030##

(149) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (100 mg, 393 μmol) and 2-fluoro-4-methylbenzoic acid (66.7 mg, 433 μmol). The product was purified with preparative HPLC to yield 27 mg (18%) of the title compound as a white solid. LC-MS: m/z=391.3 [M+H].sup.+.

Example 11

4-Methoxy-2-methyl-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(150) ##STR00031##

(151) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (100 mg, 393 μmol) and 4-methoxy-2-methylbenzoic acid (71.9 mg, 433 μmol). The product was isolated as a white solid. Yield 78 mg (49%). LC-MS: m/z=202.2 [M+2H].sup.2+.

Example 12

4-(2-(2-Fluoroethoxy)ethoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(152) ##STR00032##

a) Methyl 4-[2-(2-fluoroethoxy)ethoxy]benzoate

(153) ##STR00033##

(154) 2-(2-Fluoroethoxy)ethyl 4-methylbenzenesulfonate (CAS Nr. 1118567-11-5) (892 mg, 3.4 mmol) was dissolved under inert atmosphere at 22° C. in DMF (17 ml). Methyl 4-hydroxybenzoate (517 mg, 3.4 mmol) was added followed by Cs.sub.2CO.sub.3 (2.22 g, 6.8 mmol), then the mixture was warmed to 50° C. and stirred at 50° C. for 4 h. H.sub.2O (50 ml) was added and the product was extracted with EtOAc (3×50 ml). The organic layers were combined and dried over MgSO.sub.4 (5 g), filtered over a glass-frit (D3), washed with EtOAc (2×20 ml) and the filtrate was evaporated. The residue was purified by flash chromatography (silica gel, 40 g; EtOAc in heptane 0% to 50%). The corresponding pure fractions were collected to give after evaporation a colorless oil. LC-MS analysis of this material indicated the presence of 2% phenolic starting material. The solid was thus dissolved in DCM (20 ml) and washed with 10% Na.sub.2CO.sub.3 (2×20 ml) and H.sub.2O (1×20 ml). The aqueous layers were back-extracted with DCM (1×20 ml). The organic layers were combined, dried over MgSO.sub.4 (2 g), filtered over a glass-frit (D3) and washed with DCM (2×10 ml). The solvent was evaporated to give after drying in HV the title compound (715 mg, 87%) as colorless oil. LC-MS: m/z=243.1 [M+H].sup.+.

b) 4-[2-(2-Fluoroethoxy)ethoxy]benzoic acid

(155) ##STR00034##

(156) Methyl 4-(2-(2-fluoroethoxy)ethoxy)benzoate (597.6 mg, 2.47 mmol) was dissolved under inert atmosphere at 22° C. in MeOH (12 ml) and NaOH (1 M aq. sol., 9.87 ml, 9.87 mmol,) was added. The reaction mixture was stirred at 22° C. for 4 h. MeOH was removed under reduced pressure and the remaining mixture was diluted with H.sub.2O (10 ml), washed with DCM (2×10 ml) and treated with HCl (1 M aq., 9.87 ml, 9.87 mmol). The product was extracted with EtOAc (2×15 ml), the organic layers were combined and washed with H.sub.2O (1×10 ml), then dried over MgSO.sub.4 (2 g), filtered over a glass-frit (D3), washed with EtOAc (2×10 ml) and the filtrate was evaporated at 40° C. to give the title compound (540.4 mg, 96%) as white solid. LC-MS: m/z=229.1 [M+H].sup.+.

c) 4-(2-(2-Fluoroethoxy)ethoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(157) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (100 mg, 393 μmol) and 4-(2-(2-fluoroethoxy)ethoxy)benzoic acid (98.7 mg, 433 μmol). The product was isolated as a white solid. 122 mg (67%). LC-MS: m/z=233.2 [M+2H].sup.2+.

Example 13

4-Methoxy-N-[4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]benzamide

(158) ##STR00035##

a) 2-[4-(4-Nitrophenyl)piperazin-1-yl]-1,3-thiazole

(159) ##STR00036##

(160) 2-(Piperazin-1-yl)thiazole (596 mg, 3.52 mmol) was dissolved in DMSO (2.5 ml). K.sub.2CO.sub.3 (734 mg, 7.41 mmol) and 1-fluoro-4-nitrobenzene (500 mg, 3.54 mmol) were added and the solution was stirred at 90° C. for 20 min. The solution was diluted in H.sub.2O and extracted with DCM. The combined organic layers were washed with brine, dried over MgSO.sub.4, filtered and concentrated under vacuum. The crude product was purified by flash-column chromatography (0 to 5% MeOH in DCM) to yield 2-[4-(4-nitrophenyl)piperazin-1-yl]-1,3-thiazole (966 mg, 94%). LC-MS: m/z=291.1 [M+H].sup.+.

b) 4-[4-(1,3-Thiazol-2-yl)piperazin-1-yl]aniline

(161) ##STR00037##

(162) 2-[4-(4-Nitrophenyl)piperazin-1-yl]-1,3-thiazole (965 mg, 3.32 mmol) was combined with EtOH (2.8 ml) and THF (5.6 ml) to give an orange suspension. Hydrazine mono hydrate (666 mg, 645 μl, 13.3 mmol) and a Raney Nickel (50% slurry in H.sub.2O, 14.2 mg, 166 μmol) were added. The resulting mixture was stirred under N.sub.2 at rt for 45 min. The reaction mixture was filtered under N2 through Celite. The filtrate was evaporated to dryness to afford the desired product 4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]aniline (818.5 mg, 90%) as a brown solid. LC-MS: m/z=261.1 [M+H].sup.+.

c) 4-Methoxy-N-[4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]benzamide

(163) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]aniline (53 mg, 204 μmol) and 4-methoxybenzoic acid (34.1 mg, 224 μmol). Yield 12.5 mg (15%). Off-white solid. LC-MS: m/z=395.2 [M+H].sup.+.

Example 14

N-(4-(4-(Pyridin-2-yl)piperazin-1-yl)phenyl)-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxamide

(164) ##STR00038##

(165) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (70 mg, 275 μmol) and 2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylic acid (49.6 mg, 275 μmol). Yield 65 mg (57%). Off-white solid. LC-MS: m/z=417.2 [M+H].sup.+.

Example 15

N-(4-(4-(Pyridin-2-yl)piperazin-1-yl)phenyl)benzo[d][1,3]dioxole-5-carboxamide

(166) ##STR00039##

(167) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (70 mg, 275 μmol) and benzo[d][1,3]dioxole-5-carboxylic acid (45.7 mg, 275 μmol). Yield 71 mg (64%). Off-white solid. LC-MS: m/z=403.2 [M+H].sup.+.

Example 16

N-(4-(4-(Pyridin-2-yl)piperazin-1-yl)phenyl)imidazo[1,2-a]pyridine-7-carboxamide

(168) ##STR00040##

(169) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (70 mg, 275 μmol) and imidazo[1,2-a]pyridine-7-carboxylic acid (44.6 mg, 275 μmol). Yield 47 mg (43%). Yellow solid. LC-MS: m/z=397.3 [M−H].sup.−.

Example 17

N-(4-(4-(Pyridin-2-yl)piperazin-1-yl)phenyl)imidazo[1,2-a]pyridine-6-carboxamide

(170) ##STR00041##

(171) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (70 mg, 275 μmol) and imidazo[1,2-a]pyridine-6-carboxylic acid (44.6 mg, 275 μmol). The product was purified by preparative HPLC yielding 8.5 mg (7.7%) of the title compound as white solid. LC-MS: m/z=200.2 [M+2H].sup.2+.

Example 18

2-Fluoro-4-methoxy-N-[4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]benzamide

(172) ##STR00042##

(173) 2-Fluoro-4-methoxybenzoic acid (35.9 mg, 211 μmol) was combined with DMF (0.6 ml) to give a colorless solution. HATU (87.6 mg, 230 μmol) and DIPEA (49.6 mg, 67.1 μl, 384 μmol) were added and the reaction mixture was stirred at rt for 30 min. 4-[4-(1,3-Thiazol-2-yl)piperazin-1-yl]aniline (Intermediate 13.b, 50 mg, 192 μmol) dissolved in 0.1 ml DMF was added and the reaction mixture was stirred at rt for 1 h. H.sub.2O was added (10 ml) and the brown solution was extracted with DCM (3×10 ml). The combined organic layers were washed with brine (1×10 ml), dried over MgSO.sub.4, filtered and evaporated. The remaining brown oil was diluted with DCM (ca. 2 ml) and left over night at 4° C. Solids were collected by filtration, washed with DCM and dried under high vacuum to give 2-fluoro-4-methoxy-N-[4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]benzamide (12.4 mg, 15% yield) as white solid. The filtrate was evaporated and the residue was purified by preparative HPLC to yield a second portion of product (8.5 mg, 7.7%) as white solid. Combined yield 20.9 mg (23%). LCMS: m/z=413.2 [M+H].sup.+.

Example 19

4-Methoxy-2-methyl-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide

(174) ##STR00043##

a) 1-(5-Nitropyridin-2-yl)-4-(pyridin-2-yl)piperazine

(175) ##STR00044##

(176) To a solution of 1-(pyridin-2-yl)piperazine (5.00 g, 30.6 mmol) in DMF (150 ml) under N.sub.2 at 25° C. was added K.sub.2CO.sub.3 (8.46 g, 61.3 mmol) and the mixture was stirred at 25° C. for 30 min. 2-Chloro-5-nitropyridine (5.32 g, 33.7 mmol) was added at 25° C. and stirring was continued at 25° C. for 4 h. The reaction mixture was poured into H.sub.2O (100 ml) and extracted with EtOAc (4×250 ml). The organic phase was washed with brine, dried over Na.sub.2SO.sub.4 and solvents were evaporated. The resulting crude was purified by flash chromatography (30-80% EtOAc in hexane) to get 1-(5-nitropyridin-2-yl)-4-(pyridin-2-yl)piperazine (8.0 g, 92%) as yellow solid. LC-MS: m/z=286.3 [M+H].sup.+.

b) 6-[4-(Pyridin-2-yl)piperazin-1-yl]pyridin-3-amine

(177) ##STR00045##

(178) To a solution of 1-(5-nitropyridin-2-yl)-4-(pyridin-2-yl)piperazine (2.5 g, 8.76 mmol) in EtOH (150 ml) was added Raney-Ni (50% in H.sub.2O) (6 ml) at 25° C. Hydrazine monohydrate (2.9 ml, 59.6 mmol) was added over a period of 15 min. The resulting reaction mixture was heated to 45° C. for 1 h. After total consumption of starting material (monitored by TLC) Raney-Ni was filtered off, washed with EtOH (2×100 ml) and the filtrate was concentrated under vacuum. The resulting crude product was purified by flash chromatography (amino modified silica gel; 60% EtOAc in hexane) to get 6-[4-(pyridin-2-yl)piperazin-1-yl]pyridin-3-amine (1.7 g, 76%) as grey solid. LC-MS: m/z=255.7 [M+H].sup.+.

c) 4-Methoxy-2-methyl-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide

(179) To a solution of 4-methoxy-2-methylbenzoic acid (100 mg, 0.65 mmol) in DMF (2.5 ml) were added DIPEA (0.3 ml, 1.95 mmol), HATU (370 mg, 0.97 mmol) and 6-[4-(pyridin-2-yl)piperazin-1-yl]pyridin-3-amine (166 mg, 0.65 mmol). The reaction mixture was stirred at 25° C. for 16 h. After total consumption of starting material (monitored by TLC) the reaction mixture was poured into H.sub.2O (20 ml) and extracted with EtOAc (2×50 ml). The organic phase was dried over Na.sub.2SO.sub.4 and solvents were evaporated. The resulting crude material was purified by preparative HPLC to get the title compound (60 mg, 23%) as off-white solid. LC-MS: m/z=404.1 [M+H].sup.+.

Example 20

4-(Dimethylamino)-N-[4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]benzamide

(180) ##STR00046##

(181) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]aniline (Intermediate 13.b, 50 mg, 192 μmol) and 4-(dimethylamino)benzoic acid (34.9 mg, 211 μmol). The product was purified by preparative HPLC to yield 11.7 mg (14%) of the title compound as white solid. LC-MS: m/z=408.2 [M+H].sup.+; 204.7 [M+2H].sup.2+.

Example 21

2-Fluoro-4-methyl-N-[4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]benzamide

(182) ##STR00047##

(183) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]aniline (Intermediate 13.b, 50 mg, 192 μmol) and 2-fluoro-4-methylbenzoic acid (32.6 mg, 211 μmol). The product was purified by preparative HPLC to yield 30.4 mg (38%) of the title compound off-white solid. LC-MS: m/z=397.2 [M+H].sup.+.

Example 22

4-(4-Methylpiperazin-1-yl)-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide

(184) ##STR00048##

(185) To a solution of 4-(4-methylpiperazin-1-yl)benzoic acid (100 mg, 0.45 mmol) in DMF (3 ml) were added DIPEA (0.23 ml, 1.36 mmol), HATU (259 mg, 0.68 mmol) and 6-[4-(pyridin-2-yl)piperazin-1-yl]pyridin-3-amine (Intermediate 19.b) (116 mg, 0.45 mmol). Then the reaction mixture was stirred at 25° C. for 16 h. After total consumption of the starting material (monitored by TLC) the reaction mixture was poured into H.sub.2O (20 ml) and extracted with EtOAc (2×50 ml). The combined organic phases were dried over Na.sub.2SO.sub.4 and solvents were evaporated. The product was purified by preparative HPLC to get the title compound (24 mg, 12%) as yellow solid. LC-MS: m/z=458.2 [M+H].sup.+.

Example 23

2-Fluoro-4-methyl-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide

(186) ##STR00049##

(187) The title compound was prepared in analogy to 4-(4-methylpiperazin-1-yl)-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide (Example 22) from 6-[4-(pyridin-2-yl)piperazin-1-yl]pyridin-3-amine (Intermediate 19.b) (116 mg, 0.45 mmol) and 2-fluoro-4-methylbenzoic acid (100 mg, 0.65 mmol). Yield 77 mg (30%). White solid. LC-MS: m/z=392.4 [M+H].sup.+.

Example 24

4-Methoxy-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide

(188) ##STR00050##

(189) The title compound was prepared in analogy to 4-(4-methylpiperazin-1-yl)-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide (Example 22) from 6-[4-(pyridin-2-yl)piperazin-1-yl]pyridin-3-amine (Intermediate 19.b) (101 mg, 0.39 mmol) and 4-methoxybenzoic acid (50 mg, 0.33 mmol). Yield 17 mg (13%). Off-white solid. LC-MS: m/z=390.2 [M+H].sup.+.

Example 25

5-Methyl-N-[4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]pyridine-2-carboxamide

(190) ##STR00051##

(191) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]aniline (Intermediate 13.b) (100 mg, 384 μmol) and 5-methylpicolinic acid (57.9 mg, 422 μmol). The product was purified by preparative HPLC to yield 21.8 mg (14%) of the title compound as light green solid. LC-MS: m/z=380.2 [M+H].sup.+.

Example 26

4-Morpholin-4-yl-N-[4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]benzamide

(192) ##STR00052##

(193) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]aniline (Intermediate 13.b) (100 mg, 384 μmol) and 4-morpholinobenzoic acid (87.6 mg, 422 μmol). Yield 78 mg (43%). Light yellow solid. LC-MS: m/z=448.3 [M−H].sup.−.

Example 27

4-Methyl-N-[4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]benzamide

(194) ##STR00053##

(195) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]aniline (Intermediate 13.b) (55.8 mg, 214 μmol) and 4-methylbenzoic acid (32.1 mg, 236 μmol). The product was purified by preparative HPLC to yield 50.2 mg (59%) of the title compound as off-white solid. LC-MS: m/z=379.2 [M+H].sup.+.

Example 28

4-(4-Methylpiperazin-1-yl)-N-[4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]phenyl]benzamide

(196) ##STR00054##

(197) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]aniline (Intermediate 13.b) (79 mg, 303 μmol) and 4-(4-methylpiperazin-1-yl)benzoic acid (73.5 mg, 334 μmol). Yield 24.9 mg (14%). Off-white solid. LC-MS: m/z=463.2 [M+H].sup.+.

Example 29

2-Fluoro-4-methoxy-N-(2-methyl-4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(198) ##STR00055##

(199) The title compound was prepared in analogy to N-(4-(4-(4-cyanophenyl)piperazin-1-yl)phenyl)-6-methoxynicotinamide (Example 157) and the general synthesis of sub-series 2. Final amide coupling step by procedure B. Yield: 4 mg.

(200) .sup.1H NMR (400 MHz, DMSO): δ 9.37 (d, J=3.0 Hz, 1H), 8.15 (dd, J=1.6, 4.9 Hz, 1H), 7.70 (dd, J=8.7, 8.7 Hz, 1H), 7.60-7.54 (m, 1H), 7.30 (d, J=8.7 Hz, 1H), 6.97 (d, J=2.3 Hz, 1H), 6.95-6.88 (m, 3H), 6.85 (dd, J=2.4, 8.7 Hz, 1H), 6.68 (dd, J=4.9, 6.8 Hz, 1H), 3.84 (s, 3H), 3.64 (dd, J=5.1, 5.1 Hz, 4H), 3.23 (dd, J=5.0, 5.0 Hz, 4H), 2.22 (s, 3H). LC-MS: Rt=2.76 min, m/z=421 [M+H].sup.+.

Example 30

4-(Dimethylamino)-N-(4-(4-(6-methylpyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(201) ##STR00056##

(202) The title compound was prepared in analogy to N-(4-(4-(4-cyanophenyl)piperazin-1-yl)phenyl)-6-methoxynicotinamide (Example 157) and the general synthesis of sub-series 2. Final amide coupling step by procedure B. Yield: 70 mg.

(203) .sup.1H NMR (400 MHz, CDCl.sub.3): δ 7.77 (d, J=8.9 Hz, 2H), 7.59 (s, 1H), 7.56-7.50 (m, 2H), 7.40 (dd, J=7.8, 7.8 Hz, 1H), 6.98 (d, J=8.9 Hz, 2H), 6.71 (d, J=8.9 Hz, 2H), 6.54-6.48 (m, 2H), 3.72-3.67 (m, 4H), 3.26 (dd, J=5.1, 5.1 Hz, 4H), 3.04 (s, 6H), 2.42 (s, 3H). LC-MS: Rt=2.72 min, m/z=416 [M+H].sup.+.

Example 31

4-(Dimethylamino)-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide

(204) ##STR00057##

(205) The title compound was prepared in analogy to 4-(4-methylpiperazin-1-yl)-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide (Example 22) from 6-[4-(pyridin-2-yl)piperazin-1-yl]pyridin-3-amine (Intermediate 19.b) (155 mg, 0.61 mmol) and 4-(dimethylamino)benzoic acid (100 mg, 0.61 mmol). Yield 36 mg (15%). Off-white solid. LC-MS: m/z=403.1 [M+H].sup.+.

Example 32

4-Morpholino-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide

(206) ##STR00058##

(207) The title compound was prepared in analogy to 4-(4-methylpiperazin-1-yl)-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide (Example 22) from 6-[4-(pyridin-2-yl)piperazin-1-yl]pyridin-3-amine (Intermediate 19.b) (123 mg, 0.48 mmol) and 4-(morpholin-4-yl)benzoic acid (100 mg, 0.48 mmol). Yield 28 mg (13%). Off-white solid. LC-MS: m/z=445.1 [M+H].sup.+.

Example 33

5-Methyl-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]pyridine-2-carboxamide

(208) ##STR00059##

(209) The title compound was prepared in analogy to 4-(4-methylpiperazin-1-yl)-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide (Example 22) from 6-[4-(pyridin-2-yl)piperazin-1-yl]pyridin-3-amine (Intermediate 19.b, 186 mg, 0.73 mmol) and 5-methylpyridine-2-carboxylic acid (100 mg, 0.73 mmol). Yield 28 mg (10%). Off-white solid. LC-MS: m/z=375.2 [M+H].sup.+.

Example 34

2-Fluoro-4-methoxy-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide

(210) ##STR00060##

(211) To a solution of 6-[4-(pyridin-2-yl)piperazin-1-yl]pyridin-3-amine (Intermediate 19.b) (100 mg, 0.39 mmol) in THF (2.5 ml) cooled with an ice/H.sub.2O bath were added Et.sub.3N (0.1 ml, 0.78 mmol) and 2-fluoro-4-methoxybenzoyl chloride (74 mg, 0.39 mmol). The mixture was stirred 1 h at 0° C. The reaction mixture was washed with H.sub.2O (10 ml) and extracted with EtOAc (2×30 ml). The combined organic layers were dried over Na.sub.2SO.sub.4 and concentrated.

(212) The resulting crude material was purified by preparative HPLC to get the title compound (56 mg, 35%) as off-white solid. LC-MS: m/z=408.2 [M+H].sup.+.

Example 35

4-Methyl-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide

(213) ##STR00061##

(214) The title compound was prepared in analogy to 4-(4-methylpiperazin-1-yl)-N-[6-[4-(2-pyridyl)piperazin-1-yl]-3-pyridyl]benzamide (Example 22) from 6-[4-(pyridin-2-yl)piperazin-1-yl]pyridin-3-amine (Intermediate 19.b, 188 mg, 0.73 mmol) and 4-methylbenzoic acid (100 mg, 0.73 mmol). Yield 55 mg (20%). Off-white solid. LC-MS: m/z=371.1 [M+H].sup.+.

Example 36

4-(Dimethylamino)-N-[6-[4-(2-pyridyl)piperazin-1-yl]pyridazin-3-yl]benzamide

(215) ##STR00062##

a) 6-[4-(Pyridin-2-yl)piperazin-1-yl]pyridazin-3-amine

(216) ##STR00063##

(217) To a solution of 1-(pyridin-2-yl)piperazine (600 mg, 3.68 mmol) in DMSO (10 ml) was added 6-iodopyridazin-3-amine (813 mg, 3.68 mmol) and the reaction mixture was degassed by passing through it N.sub.2 for 15 min. K.sub.3PO.sub.4 (1.17 g, 5.51 mmol), L-hydroxyproline (193 mg, 1.48 mmol) and CuI (140 mg, 0.74 mmol) were added to the reaction mixture. After degassing with a N.sub.2 steam for 15 min, the reaction mixture was stirred at 100° C. for 16 h. The reaction mixture was poured into H.sub.2O (50 ml) and extracted with a mixture of 15% IPA/CHCl.sub.3 (3×100 ml). The combined organic layers were washed with brine, dried over Na.sub.2SO.sub.4 and solvents were evaporated. The resulting crude was purified by column chromatography (amine modified silica, 10% MeOH/DCM) to get 6-[4-(pyridin-2-yl)piperazin-1-yl]pyridazin-3-amine (160 mg, 26%) as grey solid. LC-MS: m/z=257.1 [M+H].sup.+.

b) 4-(Dimethylamino)-N-[6-[4-(2-pyridyl)piperazin-1-yl]pyridazin-3-yl]benzamide

(218) To a solution of 4-(dimethylamino)benzoic acid (75 mg, 0.46 mmol) in DMF (2.5 ml) were added DIPEA (0.23 ml, 1.36 mmol), EDC.HCl (130 mg, 0.68 mmol), HOBt (73 mg, 0.55 mmol) and 6-[4-(pyridin-2-yl)piperazin-1-yl]pyridazin-3-amine (117 mg, 0.46 mmol). The reaction mixture was stirred 16 h at 25° C. The mixture was poured into H.sub.2O (20 ml) and extracted with EtOAc (2×50 ml). The combined organic layers were dried over Na.sub.2SO.sub.4 and solvents were evaporated. The resulting crude material was purified by preparative HPLC to get the title compound (36 mg, 20%) as off-white solid. LC-MS: m/z=404.2 [M+H].sup.+.

Example 37

4-Methyl-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide

(219) ##STR00064##

a) 1-(4-Nitrophenyl)-4-pyridin-3-ylpiperazine

(220) ##STR00065##

(221) 1-Fluoro-4-nitrobenzene (500 mg, 3.54 mmol) was combined with DMSO (3.5 ml) to give a yellow solution. K.sub.2CO.sub.3 (735 mg, 5.32 mmol) and 1-(pyridin-3-yl)piperazine (868 mg, 5.32 mmol) were added and the yellow reaction mixture was stirred at 90° C. for 3 h. The reaction mixture was diluted with H.sub.2O (20 ml) and washed with DCM (3×20 ml). The combined organic layers were washed with brine (1×20 ml), dried over MgSO.sub.4 and evaporated under reduced pressure to get the crude material as a yellow solid. The crude product was purified by chromatography (50 g silica gel cartridge, DCM to DCM/MeOH 95:5, 0-10% in 20 min) to afford 1-(4-nitrophenyl)-4-(pyridin-3-yl)piperazine (747 mg, 70%) as an orange solid. LC-MS: m/z=285.2 [M+H].sup.+.

b) 4-(4-Pyridin-3-ylpiperazin-1-yl)aniline

(222) ##STR00066##

(223) 1-(4-Nitrophenyl)-4-(pyridin-3-yl)piperazine (720 mg, 2.53 mmol) was combined with EtOH (100 ml) to give an orange slurry. Pd/C 10% (270 mg, 253 μmol) was added and the reaction mixture was stirred 80 min under H.sub.2 at rt. The catalyst was filtered off over Dicalite, the volatiles were evaporated and the crude material was purified by flash chromatography (70 g silica gel cartridge, DCM to DCM/MeOH 95:5, 0-40% in 25 min). Yield 815 mg (100%). Light yellow solid. LC-MS: m/z=255.2 [M+H].sup.+.

c) 4-Methyl-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide

(224) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(pyridin-3-yl)piperazin-1-yl)aniline (70 mg, 275 μmol) and 4-methylbenzoic acid (41.2 mg, 303 μmol). The product was purified by flash chromatography (DCM to 90:2 DCM:MeOH). Residual DIPEA was removed by washing with 0.1 M citric acid and extraction with DCM. Yield 49 mg (46%). Off-white solid. LC-MS: m/z=187.1 [M+2H].sup.2+.

Example 38

4-Methoxy-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide

(225) ##STR00067##

(226) 4-Methoxybenzoic acid (46.1 mg, 303 μmol) was combined with DMF (0.6 ml) to give a colorless solution. HATU (126 mg, 330 μmol) and DIPEA (71.1 mg, 96.1 μl, 550 μmol) were added and the reaction mixture was stirred 30 min at rt. 4-(4-(Pyridin-3-yl)piperazin-1-yl)aniline (Intermediate 37.b) (70 mg, 275 μmol) was added followed by more DMF (0.3 ml). The resulting slurry was stirred at rt for 4 h. H.sub.2O was added (15 ml), then 0.1 M citric acid. After addition of DCM (5 ml) a solid formed, which was collected by filtration and washed with MeOH. The material was dried under vacuum to yield 4-methoxy-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide (35 mg, 31%). Off-white solid. LC-MS: m/z=195.1 [M+2H].sup.2+.

Example 39

4-Morpholino-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide

(227) ##STR00068##

(228) The title compound was prepared in analogy to 4-methoxy-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide (Example 38) from 4-(4-pyridin-3-ylpiperazin-1-yl)aniline (Intermediate 37.b) (70 mg, 275 μmol) and 4-morpholinobenzoic acid (62.7 mg, 303 μmol). 101 mg (79%). Off-white solid. LC-MS: m/z=222.7 [M+2H].sup.2+.

Example 40

2-Fluoro-4-methoxy-N-[6-[4-(2-pyridyl)piperazin-1-yl]pyridazin-3-yl]benzamide

(229) ##STR00069##

(230) The title compound was prepared in analogy to 4-(dimethylamino)-N-[6-[4-(2-pyridyl)piperazin-1-yl]pyridazin-3-yl]benzamide (Example 36, step b) from 6-[4-(pyridin-2-yl)piperazin-1-yl]pyridazin-3-amine (Intermediate 36.a) (83 mg, 0.44 mmol) and 2-fluoro-4-methoxybenzoic acid (75 mg, 0.44 mmol). 18 mg (10%). Off-white solid. LC-MS: m/z=409.1 [M+H].sup.+.

Example 41

4-Methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide

(231) ##STR00070##

a) 4-[4-(4-Pyridyl)piperazin-1-yl]aniline

(232) ##STR00071##

(233) To a solution of 1-(pyridin-4-yl)piperazine (300 mg, 1.81 mmol) in DMSO (5 ml) in a sealed tube at 25° C. were added 4-iodoaniline (477 mg, 2.18 mmol), K.sub.3PO.sub.4 (1.16 g, 5.45 mmol) and the reaction mixture was degassed with argon for 15 min. L-Hydroxyproline (95 mg, 0.73 mmol) and CuI (69 mg, 0.36 mmol) were added to the reaction mixture and it was again degassed for 15 min. Then the reaction mixture was stirred at 100° C. for 16 h. The reaction mixture was poured into H.sub.2O (50 ml) and extracted with 15% IPA in CHCl.sub.3 (3×100 ml). The combined organic layers were washed with brine, dried over Na.sub.2SO.sub.4 and solvents were evaporated. The resulting crude product was purified by column chromatography (amine-modified silica; 5% MeOH in DCM) to get 4-[4-(4-pyridyl)piperazin-1-yl]aniline (240 mg, 52%) as grey sticky solid. LC-MS: m/z=255.1 [M+H].sup.+.

b) 4-Methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide

(234) To a solution of 4-methoxybenzoic acid (100 mg, 0.66 mmol) in DMF (3 ml) were added DIPEA (0.33 ml, 1.97 mmol), EDC.HCl (168 mg, 0.99 mmol), HOBt (107 mg, 0.79 mmol) and 4-[4-(4-pyridyl)piperazin-1-yl]aniline (167 mg, 0.66 mmol). Then the reaction mixture was stirred at 25° C. for 16 h. The reaction mixture was poured into H.sub.2O (20 ml) and extracted with EtOAc (2×50 ml). The combined organic layers were dried (Na.sub.2SO.sub.4) and evaporated. The resulting material was purified by prep-HPLC to get 4-methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide (17 mg, 7%) as off-white solid. LC-MS: m/z=389.1 [M+H].sup.+.

Example 42

4-Methyl-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-carboxamide

(235) ##STR00072##

(236) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (70 mg, 275 μmol) and 4-methyl-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-carboxylic acid (58.5 mg, 303 μmol). Yield 55 mg (44%). White solid. LC-MS: m/z=430.1 [M+H].sup.+.

Example 43

4-Methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide

(237) ##STR00073##

a) 1-(6-Nitropyridin-3-yl)-4-pyridin-2-ylpiperazine

(238) ##STR00074##

(239) 5-Fluoro-2-nitropyridine (500 mg, 3.52 mmol) was combined with DMSO (5 ml) to give a yellow solution. K.sub.2CO.sub.3 (730 mg, 5.28 mmol) and 1-(pyridin-2-yl)piperazine (862 mg, 804 μl) were added and the reaction mixture was stirred at 90° C. for 2 hours. The reaction mixture was diluted with H.sub.2O (20 ml) and washed with DCM (3×20 ml). The combined organic layers were washed with brine (1×20 ml), dried over MgSO.sub.4 and evaporated under reduced pressure to get the crude material as an orange solid. This crude product was used without further purification in the next step. LC-MS: m/z=286.2 [M+H].sup.+.

b) 5-(4-(Pyridin-2-yl)piperazin-1-yl)pyridin-2-amine

(240) ##STR00075##

(241) 1-(6-Nitropyridin-3-yl)-4-pyridin-2-ylpiperazine (1.33 g, 4.67 mmol) was dissolved in EtOH (50 ml) and under an inert atmosphere Pd/C 10% (200 mg, 4.67 mmol) was added. The reaction mixture was stirred under H.sub.2 at rt for 2 h, then solids were removed by filtration over Celite. The filtrate was concentrated under vacuum and the crude material was purified by flash chromatography (DCM to 20:1:0.1 DCM:MeOH:NH.sub.3 aq.) to yield the title compound (878 mg, 70%) as a light brown solid. LC-MS: m/z=128.6 [M+2H].sup.2+.

c) 4-Methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide

(242) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-amine (70 mg, 274 μmol) and 4-methoxybenzoic acid (45.9 mg, 302 μmol).

(243) Yield 107 mg (56%). White solid. LC-MS: m/z=195.7 [M+2H].sup.2+.

Example 44

2-Fluoro-4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide

(244) ##STR00076##

(245) The title compound was prepared in analogy to 4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide (Example 43, step c) from 5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-amine (Intermediate 43.b) (70 mg, 274 μmol) and 2-fluoro-4-methoxybenzoic acid (51.3 mg, 302 μmol). Yield 85 mg (75%). White solid. LC-MS: m/z=204.7 [M+2H].sup.2+.

Example 45

4-Methyl-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide

(246) ##STR00077##

(247) The title compound was prepared in analogy to 4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide (Example 43.c) from 5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-amine (Intermediate 43.b (70 mg, 274 μmol) and 4-methylbenzoic acid (41.1 mg, 302 μmol). Yield 61 mg (59%). White solid. LC-MS: m/z=187.6 [M+2H].sup.2+.

Example 46

4-(Dimethylamino)-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide

(248) ##STR00078##

(249) The title compound was prepared in analogy to 4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide (Example 43.c) from 5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-amine (Intermediate 43.b) (70 mg, 274 μmol) and 4-(dimethylamino)benzoic acid (49.8 mg, 302 μmol). Yield 40 mg (35%). White solid. LC-MS: m/z=202.3 [M+2H].sup.2+.

Example 47

2-Fluoro-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide

(250) ##STR00079##

(251) The title compound was prepared in analogy to 4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide (Example 43.c) from 5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-amine (Intermediate 43.b) (70 mg, 274 μmol) and 2-fluorobenzoic acid (42.3 mg, 302 μmol). Yield 71 mg (67%). White solid. LC-MS: m/z=189.6 [M+2H].sup.2+.

Example 48

4-Morpholino-N-[6-[4-(2-pyridyl)piperazin-1-yl]pyridazin-3-yl]benzamide

(252) ##STR00080##

(253) The title compound was prepared in analogy to 4-(dimethylamino)-N-[6-[4-(2-pyridyl)piperazin-1-yl]pyridazin-3-yl]benzamide (Example 36, step b) from 6-[4-(pyridin-2-yl)piperazin-1-yl]pyridazin-3-amine (Intermediate 36.a) (93 mg, 0.36 mmol) and 4-morpholinobenzoic acid (75 mg, 0.36 mmol). Yield 16 mg (10%). Off-white solid. LC-MS: m/z=446.0 [M+H].sup.+.

Example 49

4-Methoxy-N-{4-[4-(pyrimidin-2-yl)piperazin-1-yl]phenyl}benzamide

(254) ##STR00081##

a) 4-[4-(Pyrimidin-2-yl)piperazin-1-yl]aniline

(255) ##STR00082##

(256) The title compound was prepared in analogy to 4-[4-(4-pyridyl)piperazin-1-yl]aniline (Intermediate 41.a) from 2-(piperazin-1-yl)pyrimidine (300 mg, 1.83 mmol). Yield 255 mg (55%). Black sticky solid. LC-MS: m/z=256.1 [M+H].sup.+.

b) 4-Methoxy-N-{4-[4-(pyrimidin-2-yl)piperazin-1-yl]phenyl}benzamide

(257) The title compound was prepared in analogy to 4-methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide (Example 41, step b) from 4-[4-(pyrimidin-2-yl)piperazin-1-yl]aniline (168 mg, 0.66 mmol) and 4-methoxybenzoic acid (100 mg, 0.66 mmol). Yield 45 mg (18%). Off-white solid. LC-MS: m/z=390.2 [M+H].sup.+.

Example 50

N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(258) ##STR00083##

a) 6-[4-(4-Aminophenyl)piperazin-1-yl]pyridine-3-carbonitrile

(259) ##STR00084##

Method A

(260) The title compound was prepared in analogy to 4-[4-(4-pyridyl)piperazin-1-yl]aniline (Intermediate 41.a) from 2-(piperazin-1-yl)pyridine-4-carbonitrile (300 mg, 1.59 mmol). Yield 180 mg (40%). Black sticky solid. LC-MS: m/z=280.2 [M+H].sup.+.

Method B

i) 6-[4-(4-nitrophenyl)piperazin-1-yl]pyridine-3-carbonitrile

(261) ##STR00085##

(262) 6-(Piperazin-1-yl)nicotinonitrile (3.76 g, 20 mmol) was dissolved at 20-25° C. in DMSO (15 ml) under inert atmosphere. K.sub.2CO.sub.3 (4.15 g, 30 mmol) was added at 20-25° C. followed by 1-fluoro-4-nitrobenzene (3.1 g, 2.33 ml, 22 mmol). The reaction mixture was heated to 90° C. and stirred at this temperature for 90 min. The mixture was allowed to cool to 20-25° C., leading to precipitation of the product and an instirrable solid that was left standing at 22° C. over night. The mixture was mainly dissolved in H.sub.2O and DCM and the aqueous layer (containing some solid product) was extracted with DCM. The organic layers were dried over MgSO.sub.4, filtered over a glass-frit (D3), washed with DCM, and the filtrate was evaporated under reduced pressure at 40° C. The residue was partially dissolved in DCM/MeOH 10:1 (40 ml), adsorbed on Isolute HM-N 9800, evaporated and then purified by flash chromatography (silica gel, MeOH in DCM 1% to 5%). Pure product-fractions were combined and evaporated at 40° C. to give after drying in HV the title compound (5.59 g, 90%) as an orange solid. LCMS m/z=310.2 [M+H].sup.+.

ii) 6-[4-(4-Aminophenyl)piperazin-1-yl]pyridine-3-carbonitrile

(263) ##STR00086##

(264) 6-(4-(4-Nitrophenyl)piperazin-1-yl)nicotinonitrile (10.2 g, 33 mmol) was suspended at 20-25° C. in EtOH (470 ml), and under inert atmosphere at 20-25° C. was added a slurry of Pd/C, 10% (3.51 g, 3.3 mmol) in EtOH (50 ml). The reaction mixture was set under H.sub.2 and reacted at 20-25° C. for 20 h. The catalyst was filtered off over a membrane-filter, washed with EtOH and DCM/MeOH 4:1, and the filtrate was evaporated at 40° C. to give the crude product as light yellow solid. This material was suspended in DCM/MeOH 2:1, adsorbed on Isolute HM-N 9800, evaporated and then purified by flash chromatography (silica gel, MeOH in DCM 1% to 5%). The corresponding pure fractions were collected to give after evaporation at 40° C. the title compound (5.92 g, 64%) as an off-white solid. LC-MS m/z=280.1 [M+H].sup.+.

b) N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(265) The title compound was prepared in analogy to 4-methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide (Example 41, step b) from 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-3-carbonitrile (184 mg, 0.66 mmol) and 4-methoxybenzoic acid (100 mg, 0.66 mmol). Yield 26 mg (10%). Off-white solid. LC-MS: m/z=414.4 [M+H].sup.+.

Example 51

4-Morpholino-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide

(266) ##STR00087##

(267) The title compound was prepared in analogy to 4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide (Example 43, step c) from 5-[4-(2-pyridyl)piperazin-1-yl]pyridin-2-amine (Intermediate 43.b) (70 mg, 274 μmol) and 4-morpholinobenzoic acid (62.5 mg, 302 μmol). Yield 53 mg (43%). White solid. LC-MS: m/z=223.2 [M+2H].sup.2+.

Example 52

2-Fluoro-4-methyl-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide

(268) ##STR00088##

(269) The title compound was prepared in analogy to 4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide (Example 43, step c) from 5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-amine (Intermediate 43.b) (55 mg, 215 μmol) and 2-fluoro-4-methylbenzoic acid (36 mg, 237 μmol). Yield 62 mg (73%). Off-white solid. LC-MS: m/z=196.7 [M+2H].sup.2+.

Example 53

5-Methyl-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)picolinamide

(270) ##STR00089##

(271) The title compound was prepared in analogy to 4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide (Example 43, step c) from 5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-amine (Intermediate 43.b) (55 mg, 215 μmol) and 5-methylpicolinic acid (32 mg, 237 μmol). Yield 12 mg (14%). Off-white solid. LC-MS: m/z=188.2 [M+2H].sup.2+.

Example 54

3-Methyl-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide

(272) ##STR00090##

(273) The title compound was prepared in analogy to 4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide (Example 43, step c) from 5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-amine (Intermediate 43.b) (40 mg, 157 μmol) and 3-methylbenzoic acid (33 mg, 242 μmol). Yield 40 mg (67%). Grey solid. LC-MS: m/z=187.7 [M+2H].sup.2+.

Example 55

4-Methoxy-N-{4-[4-(1,3,5-triazin-2-yl)piperazin-1-yl]phenyl}benzamide

(274) ##STR00091##

a) 4-[4-(1,3,5-Triazin-2-yl)piperazin-1-yl]aniline

(275) ##STR00092##

(276) The title compound was prepared in analogy to 4-[4-(4-pyridyl)piperazin-1-yl]aniline (Intermediate 41.a) from 2-piperazin-1-yl-1,3,5-triazine (300 mg, 1.84 mmol). Yield 175 mg (37%). Grey sticky solid. LC-MS: m/z=257.1 [M+H].sup.+.

b) 4-Methoxy-N-{4-[4-(1,3,5-triazin-2-yl)piperazin-1-yl]phenyl}benzamide

(277) The title compound was prepared in analogy to 4-methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide (Example 41, step b) from 4-[4-(1,3,5-triazin-2-yl)piperazin-1-yl]aniline (168 mg, 0.66 mmol) and 4-methoxybenzoic acid (100 mg, 0.66 mmol). Yield 22 mg (9%). Off-white solid. LC-MS: m/z=391.2 [M+H].sup.+.

Example 56

4-Methoxy-N-{4-[4-(pyrimidin-4-yl)piperazin-1-yl]phenyl}benzamide

(278) ##STR00093##

a) 4-[4-(Pyrimidin-4-yl)piperazin-1-yl]aniline

(279) ##STR00094##

(280) The title compound was prepared in analogy to 4-[4-(4-pyridyl)piperazin-1-yl]aniline (Intermediate 41.a) from 4-(piperazin-1-yl)pyrimidine (300 mg, 1.83 mmol). Yield 188 mg (40%). Black solid. LC-MS: m/z=256.0 [M+H].sup.+.

b) 4-Methoxy-N-{4-[4-(pyrimidin-4-yl)piperazin-1-yl]phenyl}benzamide

(281) The title compound was prepared in analogy to 4-methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide (Example 41, step b) from 4-[4-(pyrimidin-4-yl)piperazin-1-yl]aniline (168 mg, 0.66 mmol) and 4-methoxybenzoic acid (100 mg, 0.66 mmol). Yield 42 mg (16%). Off-white solid. LC-MS: m/z=390.2 [M+H].sup.+.

Example 57

N-[4-[4-(4-Cyanophenyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide

(282) ##STR00095##

a) 4-[4-(4-Aminophenyl)piperazin-1-yl]benzonitrile

(283) ##STR00096##

(284) The title compound was prepared in analogy to 4-[4-(4-pyridyl)piperazin-1-yl]aniline (Intermediate 41.a) from 4-(piperazin-1-yl)benzonitrile (300 mg, 1.60 mmol). Yield 210 mg (47%). Black solid. LC-MS: m/z=279.2 [M+H].sup.+.

b) N-[4-[4-(4-Cyanophenyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide

(285) The title compound was prepared in analogy to 4-methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide (Example 41, step b) from 4-[4-(4-aminophenyl)piperazin-1-yl]benzonitrile (183 mg, 0.66 mmol) and 4-methoxybenzoic acid (100 mg, 0.66 mmol). Yield 26 mg (10%). Off-white solid. LC-MS: m/z=413.2 [M+H].sup.+.

Example 58

4-Methoxy-N-[4-[4-(6-methoxypyridin-3-yl)piperazin-1-yl]phenyl]benzamide

(286) ##STR00097##

a) 4-(4-(6-Methoxypyridin-3-yl)piperazin-1-yl)aniline

(287) ##STR00098##

(288) 1-(6-Methoxypyridin-3-yl)-4-(4-nitrophenyl)piperazine (80 mg, 255 μmol) (CAS Nr. 158399-77-0) was combined with EtOH (5.0 ml) to give a yellow slurry. Pd/C 10% (27.1 mg, 25.5 μmol) was added and the reaction mixture was stirred under H.sub.2 at rt for 80 min. The catalyst was filtered off over Dicalite, volatiles were evaporated and the crude material was purified by preparative TLC (silica gel, 2 mm, 9:1 DCM/MeOH) to obtain 4-(4-(6-methoxypyridin-3-yl)piperazin-1-yl)aniline (44 mg, 59%) as an off-white solid. LC-MS: m/z=285.2 [M+H].sup.+.

b) 4-Methoxy-N-[4-[4-(6-methoxypyridin-3-yl)piperazin-1-yl]phenyl]benzamide

(289) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(6-methoxypyridin-3-yl)piperazin-1-yl)aniline (43.7 mg, 154 μmol) and 4-methoxybenzoic acid (25.7 mg, 169 μmol). Yield 4.5 mg (6.6%). White solid. LC-MS: m/z=419.2 [M+H].sup.+.

Example 59

4-Methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide

(290) ##STR00099##

a) 5-Nitro-2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidine

(291) ##STR00100##

(292) 2-Chloro-5-nitropyrimidine (2.0 g, 12 mmol) was dissolved in THF (60 ml). 1-(Pyridin-2-yl)piperazine (2.2 g, 2.1 ml, 14 mmol) was added. After completion of the reaction as monitored by TLC, the mixture was concentrated under vacuum. The crude was diluted with H.sub.2O and extracted with EtOAc and additional portions of DCM. The combined organic layers were dried with MgSO.sub.4 and concentrated under vacuum. The product was purified by flash chromatography (silica gel, 120 g, 0% to 5% MeOH in DCM) to yield 5-nitro-2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidine (1.07 g, 30%) as an orange solid. LC-MS: m/z=287.2 [M+H].sup.+.

b) 2-(4-(Pyridin-2-yl)piperazin-1-yl)pyrimidin-5-amine

(293) ##STR00101##

(294) 5-Nitro-2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidine (1.07 g, 3.74 mmol) was dissolved in EtOH (50 ml). The solution was purged with Ar and Pd/C 10% (350 mg, 3.74 mmol) was added. The reaction mixture was stirred under H.sub.2 at rt for 2.5 h. The solution was filtered over Celite, washed with EtOH and concentrated under vacuum to yield 2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-amine (870 mg 89% yield) as light green solid. LC-MS: m/z=129.1 [M+2H]2+.

c) 4-Methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide

(295) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-amine (60 mg, 234 μmol) and 4-methoxybenzoic acid (39.2 mg, 258 μmol). Yield 58 mg (60%). White solid. LC-MS: m/z=391.2 [M+H].sup.+.

Example 60

2-Fluoro-4-methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide

(296) ##STR00102##

(297) The title compound was prepared in analogy to 4-methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide (Example 59, step c) from 2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-amine (Intermediate 59.b) (60 mg, 234 μmol) and 2-fluoro-4-methoxybenzoic acid (43.8 mg, 258 μmol). Yield 82 mg (82%). White solid. LC-MS: m/z=409.2 [M+H].sup.+.

Example 61

2-Fluoro-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide

(298) ##STR00103##

(299) The title compound was prepared in analogy to 4-methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide (Example 59, step c) from 2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-amine (Intermediate 59.b) (60 mg, 234 μmol) and 2-fluorobenzoic acid (36.1 mg, 258 μmol). Yield 51 mg (56%). White solid. LC-MS: m/z=379.2 [M+H].sup.+.

Example 62

4-(Dimethylamino)-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide

(300) ##STR00104##

(301) The title compound was prepared in analogy to 4-methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide (Example 59, step c) from 2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-amine (Intermediate 59.b) (60 mg, 234 μmol) and 4-(dimethylamino)benzoic acid (42.5 mg, 258 μmol). Yield 75 mg (76%). Off-white solid. LC-MS: m/z=202.7 [M+2H]2+.

Example 63

4-Morpholino-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide

(302) ##STR00105##

(303) The title compound was prepared in analogy to 4-methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide (Example 59, step c) from 2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-amine (Intermediate 59.b) (60 mg, 234 μmol) and 4-morpholinobenzoic acid (53.4 mg, 258 μmol). Yield 74 mg (68%). Off-white solid. LC-MS: m/z=446.3 [M+H].sup.+.

Example 64

3-Methyl-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide

(304) ##STR00106##

(305) The title compound was prepared in analogy to 4-methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide (Example 59, step c) from 2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-amine (Intermediate 59.b) (60 mg, 234 μmol) and 3-methylbenzoic acid (35.1 mg, 258 μmol). Yield 71 mg (77%). Light brown solid. LC-MS: m/z=375.2 [M+H].sup.+.

Example 65

N-[4-[4-(4-Cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide

(306) ##STR00107##

a) 2-[4-(4-Aminophenyl)piperazin-1-yl]pyridine-4-carbonitrile

(307) ##STR00108##

(308) The title compound was prepared in analogy to 4-[4-(4-pyridyl)piperazin-1-yl]aniline (Intermediate 41.a) from 2-(piperazin-1-yl)pyridine-4-carbonitrile (300 mg, 1.59 mmol). Yield 150 mg (34%). Off-white solid. LC-MS: m/z=279.2 [M+H].sup.+.

b) N-[4-[4-(4-Cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide

(309) The title compound was prepared in analogy to 4-methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide (Example 41, step b) from 2-[4-(4-aminophenyl)piperazin-1-yl]pyridine-4-carbonitrile (184 mg, 0.66 mmol) and 4-methoxybenzoic acid (100 mg, 0.66 mmol). Yield 32 mg (12%). Off-white solid. LC-MS: m/z=414.2 [M+H].sup.+.

Example 66

4-Methoxy-N-{4-[4-(thiophen-2-yl)piperazin-1-yl]phenyl}benzamide

(310) ##STR00109##

a) 4-[4-(Thiophen-2-yl)piperazin-1-yl]aniline

(311) ##STR00110##

(312) The title compound was prepared in analogy to 4-[4-(4-pyridyl)piperazin-1-yl]aniline (Intermediate 41.a) from 1-(thiophen-2-yl)piperazine (300 mg, 1.78 mmol). Yield 220 mg (48%). Off-white solid. LC-MS: m/z=260.0 [M+H].sup.+.

b) 4-Methoxy-N-{4-[4-(thiophen-2-yl)piperazin-1-yl]phenyl}benzamide

(313) The title compound was prepared in analogy to 4-methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide (Example 41, step b) from 4-[4-(thiophen-2-yl)piperazin-1-yl]aniline (171 mg, 0.66 mmol) and 4-methoxybenzoic acid (100 mg, 0.66 mmol). Yield 10 mg (4%). Grey solid. LC-MS: m/z=394.1 [M+H].sup.+.

Example 67

4-Methoxy-N-{4-[4-(2-methoxypyridin-3-yl)piperazin-1-yl]phenyl}benzamide

(314) ##STR00111##

a) 4-[4-(2-Methoxypyridin-3-yl)piperazin-1-yl]aniline

(315) ##STR00112##

(316) The title compound was prepared in analogy to 4-[4-(4-pyridyl)piperazin-1-yl]aniline (Intermediate 41.a) from 1-(2-methoxypyridin-3-yl)piperazine (250 mg, 1.09 mmol). Yield 130 mg (42%). Black sticky solid. LC-MS: m/z=285.4 [M+H].sup.+.

b) 4-Methoxy-N-{4-[4-(2-methoxypyridin-3-yl)piperazin-1-yl]phenyl}benzamide

(317) The title compound was prepared in analogy to 4-methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide (Example 41, step b) from 4-[4-(2-methoxypyridin-3-yl)piperazin-1-yl]aniline (187 mg, 0.66 mmol) and 4-methoxybenzoic acid (100 mg, 0.66 mmol). Yield 14 mg (5%). Off-white solid. LC-MS: m/z=419.1 [M+H].sup.+.

Example 68

4-Methoxy-N-{4-[4-(6-methoxypyridin-2-yl)piperazin-1-yl]phenyl}benzamide

(318) ##STR00113##

a) 4-[4-(6-Methoxypyridin-2-yl)piperazin-1-yl]aniline

(319) ##STR00114##

(320) The title compound was prepared in analogy to 4-[4-(4-pyridyl)piperazin-1-yl]aniline (Intermediate 41.a) from 1-(6-methoxypyridin-2-yl)piperazine (300 mg, 1.55 mmol). Yield 172 mg (39%). Off-white solid. LC-MS: m/z=285.1 [M+H].sup.+.

b) 4-Methoxy-N-{4-[4-(6-methoxypyridin-2-yl)piperazin-1-yl]phenyl}benzamide

(321) The title compound was prepared in analogy to 4-methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide (Example 41, step b) from 4-[4-(6-methoxypyridin-2-yl)piperazin-1-yl]aniline (183 mg, 0.66 mmol) and 4-methoxybenzoic acid (100 mg, 0.66 mmol). Yield 62 mg (23%). Off-white solid. LC-MS: m/z=419.1 [M+H].sup.+.

Example 69

4-Methoxy-N-{4-[4-(2-methoxyphenyl)piperazin-1-yl]phenyl}benzamide

(322) ##STR00115##

a) 4-[4-(2-Methoxyphenyl)piperazin-1-yl]aniline

(323) ##STR00116##

(324) The title compound was prepared in analogy to 4-[4-(4-pyridyl)piperazin-1-yl]aniline (Intermediate 41.a) from 1-(2-methoxyphenyl)piperazine (300 mg, 1.56 mmol). Yield 190 mg (43%). Black sticky solid. LC-MS: m/z=284.2 [M+H].sup.+.

b) 4-Methoxy-N-{4-[4-(2-methoxyphenyl)piperazin-1-yl]phenyl}benzamide

(325) The title compound was prepared in analogy to 4-methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide (Example 41, step b) from 4-[4-(2-methoxyphenyl)piperazin-1-yl]aniline (186 mg, 0.66 mmol) and 4-methoxybenzoic acid (100 mg, 0.66 mmol). Yield 30 mg (11%). Off-white solid. LC-MS: m/z=418.2 [M+H].sup.+.

Example 70

N-{4-[4-(2-Cyanophenyl)piperazin-1-yl]phenyl}-4-methoxybenzamide

(326) ##STR00117##

a) 2-[4-(4-Aminophenyl)piperazin-1-yl]benzonitrile

(327) ##STR00118##

(328) The title compound was prepared in analogy to 4-[4-(4-pyridyl)piperazin-1-yl]aniline (Intermediate 41.a) from 2-(piperazin-1-yl)benzonitrile (400 mg, 2.13 mmol). Yield 160 mg (27%). Black sticky solid. LC-MS: m/z=279.3[M+H].sup.+.

b) N-{4-[4-(2-Cyanophenyl)piperazin-1-yl]phenyl}-4-methoxybenzamide

(329) The title compound was prepared in analogy to 4-methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide (Example 41, step b) from 2-[4-(4-aminophenyl)piperazin-1-yl]benzonitrile (184 mg, 0.66 mmol) and 4-methoxybenzoic acid (100 mg, 0.66 mmol). Yield 40 mg (15%). Off-white solid. LC-MS: m/z=413.1 [M+H].sup.+.

Example 71

N-{4-[4-(2-Fluorophenyl)piperazin-1-yl]phenyl}-4-methoxybenzamide

(330) ##STR00119##

a) 4-[4-(2-Fluorophenyl)piperazin-1-yl]aniline

(331) ##STR00120##

(332) The title compound was prepared in analogy to 4-[4-(4-pyridyl)piperazin-1-yl]aniline (Intermediate 41.a) from 1-(2-fluorophenyl)piperazine (500 mg, 2.77 mmol). Yield 250 mg (33%). Brown sticky solid. LC-MS: m/z=272.0 [M+H].sup.+.

b) N-{4-[4-(2-Fluorophenyl)piperazin-1-yl]phenyl}-4-methoxybenzamide

(333) The title compound was prepared in analogy to 4-methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide (Example 41, step b) from 4-[4-(2-fluorophenyl)piperazin-1-yl]aniline (179 mg, 0.66 mmol) and 4-methoxybenzoic acid (100 mg, 0.66 mmol). Yield 26 mg (10%). Grey solid. LC-MS: m/z=406.1 [M+H].sup.+.

Example 72

4-Methoxy-2-methyl-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide

(334) ##STR00121##

(335) The title compound was prepared in analogy to 4-methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide (Example 59, step c) from 2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-amine (Intermediate 59.b) (60 mg, 234 μmol) and 4-methoxy-2-methylbenzoic acid (42.8 mg, 258 μmol). Yield 77 mg (78%). Off-white solid. LC-MS: m/z=405.2 [M+H].sup.+.

Example 73

4-(4-Methylpiperazin-1-yl)-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide

(336) ##STR00122##

(337) The title compound was prepared in analogy to 4-methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide (Example 59, step c) from 2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-amine (Intermediate 59.b) (60 mg, 234 μmol) and 4-(4-methylpiperazin-1-yl)benzoic acid (56.7 mg, 258 μmol). Yield 79 mg (70%). Light red solid. LC-MS: m/z=230.3 [M+2H].sup.2.

Example 74

4-Methyl-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide

(338) ##STR00123##

(339) The title compound was prepared in analogy to 4-methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide (Example 59, step c) from 2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-amine (Intermediate 59.b) (60 mg, 234 μmol) and 4-methylbenzoic acid (35.1 mg, 258 μmol). Yield 63 mg (69%). Off-white solid. LC-MS: m/z=375.2 [M+H].sup.+.

Example 75

5-Methyl-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)picolinamide

(340) ##STR00124##

(341) The title compound was prepared in analogy to 4-methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide (Example 59, step c) from 2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-amine (Intermediate 59.b) (60 mg, 234 μmol) and 5-methylpicolinic acid (35.3 mg, 258 μmol). Yield 6 mg (6%). Off-white solid. LC-MS: m/z=376.2 [M+H].sup.+.

Example 76

5-Methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)picolinamide

(342) ##STR00125##

(343) The title compound was prepared in analogy to 4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide (Example 43, step c) from 5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-amine (Intermediate 43.b) (40 mg, 157 μmol) and 5-methoxypicolinic acid (39.6 mg, 259 μmol). Yield 45 mg (47%). Off-white solid. LC-MS: m/z=391.2 [M+H].sup.+.

Example 77

5-Methoxy-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)picolinamide

(344) ##STR00126##

(345) The title compound was prepared in analogy to 4-methyl-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide (Example 37, step c) from 4-(4-(pyridin-3-yl)piperazin-1-yl)aniline (Intermediate 37.b) (60 mg, 236 μmol) and 5-methoxypicolinic acid (39.7 mg, 260 μmol). Off white solid. LC-MS: m/z=390.2 [M+H].sup.+.

Example 78

5-Methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)picolinamide

(346) ##STR00127##

(347) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (60 mg, 236 μmol) and 5-methoxypicolinic acid (39.7 mg, 260 μmol). Yield 51 mg (53%). Light brown solid. LC-MS: m/z=390.2 [M+H].sup.+.

Example 79

5-Methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)picolinamide

(348) ##STR00128##

(349) The title compound was prepared in analogy to 4-methoxy-N-(2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)benzamide (Example 59, step c) from 2-(4-(pyridin-2-yl)piperazin-1-yl)pyrimidin-5-amine (Intermediate 59.b) (60 mg, 234 μmol) and 5-methoxypicolinic acid (39.4 mg, 258 μmol). Yield 45 mg (47%). White solid. LC-MS: m/z=392.2 [M+H].sup.+.

Example 80

4-Methoxy-2-methyl-N-[5-(4-pyridin-2-ylpiperazin-1-yl)pyridin-2-yl]benzamide

(350) ##STR00129##

(351) The title compound was prepared in analogy to 4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide (Example 43, step c) from 5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-amine (Intermediate 43.b) (70 mg, 274 μmol) and 4-methoxy-2-methylbenzoic acid (50.1 mg, 302 μmol). Yield 21 mg (18%). White solid. 1H NMR (300 MHz, CHLOROFORM-d) 6 ppm 2.54 (s, 3H) 3.22-3.28 (m, 4H) 3.69-3.75 (m, 4H) 3.83 (s, 3H) 6.65-6.80 (m, 4H) 7.28-7.41 (m, 1H) 7.49-7.56 (m, 2H) 7.85 (br s, 1H) 8.23 (d, J=4.84 Hz, 1H) 8.27 (d, J=8.98 Hz, 1H) 8.44 (br s, 1H).

Example 81

4-(4-Methylpiperazin-1-yl)-N-[5-(4-pyridin-2-ylpiperazin-1-yl)pyridin-2-yl]benzamide

(352) ##STR00130##

(353) The title compound was prepared in analogy to 4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-yl)benzamide (Example 43, step c) from 5-(4-(pyridin-2-yl)piperazin-1-yl)pyridin-2-amine (Intermediate 43.b) (70 mg, 274 μmol) and 4-(4-methylpiperazin-1-yl)benzoic acid (66.4 mg, 302 μmol). Yield 55 mg (42%). White solid. LC-MS: m/z=458.3 [M+H].sup.+.

Example 82

4-Methoxy-N-[4-[4-(4-methoxy-2-pyridyl)piperazin-1-yl]phenyl]benzamide

(354) ##STR00131##

a) 4-[4-(4-Methoxy-2-pyridyl)piperazin-1-yl]aniline

(355) ##STR00132##

(356) The title compound was prepared in analogy to 4-[4-(4-pyridyl)piperazin-1-yl]aniline (Intermediate 41.a) from 1-(4-methoxypyridin-2-yl)piperazine (300 mg, 1.55 mmol). Yield 208 mg (47%). Black sticky solid. LC-MS: m/z=285.3 [M+H].sup.+.

b) 4-Methoxy-N-[4-[4-(4-methoxy-2-pyridyl)piperazin-1-yl]phenyl]benzamide

(357) The title compound was prepared in analogy to 4-methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide (Example 41, step b) from 4-[4-(4-methoxy-2-pyridyl)piperazin-1-yl]aniline (187 mg, 0.66 mmol) and 4-methoxybenzoic acid (100 mg, 0.66 mmol). 152 mg (55%). Grey solid. LC-MS: m/z=419.0 [M+H].sup.+.

Example 83

Acetic acid; 4-Methoxy-N-[4-[4-(3-methyl-4-pyridyl)piperazin-1-yl]phenyl]benzamide

(358) ##STR00133##

a) 4-[4-(3-Methylpyridin-4-yl)piperazin-1-yl]aniline

(359) ##STR00134##

(360) The title compound was prepared in analogy to 4-[4-(4-pyridyl)piperazin-1-yl]aniline (Intermediate 41.a) from 1-(3-methylpyridin-4-yl)piperazine (300 mg, 1.69 mmol). Yield 220 mg (48%). Brown sticky solid. LC-MS: m/z=269.2[M+H].sup.+.

b) Acetic acid; 4-methoxy-N-[4-[4-(3-methyl-4-pyridyl)piperazin-1-yl]phenyl]benzamide

(361) The title compound was prepared in analogy to 4-methoxy-N-[4-[4-(4-pyridyl)piperazin-1-yl]phenyl]benzamide (Example 41, step b) from 4-[4-(3-methylpyridin-4-yl)piperazin-1-yl]aniline (176 mg, 0.66 mmol) and 4-methoxybenzoic acid (100 mg, 0.66 mmol). Yield 64 mg (24%). Brown solid. LC-MS: m/z=403.1 [M+H].sup.+.

Example 84

2-Fluoro-4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide

(362) ##STR00135##

a) 2-Chloro-5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazine

(363) ##STR00136##

(364) 1-(Pyridin-2-yl)piperazine (1.64 g, 1.53 ml, 10.1 mmol), 2,5-dichloropyrazine (1.5 g, 10.1 mmol) and Cs.sub.2CO.sub.3 (5.25 g, 16.1 mmol) were dissolved in DMF (40 ml). The solution was stirred 17 h at 55° C. The solution was diluted with H.sub.2O, then extracted with DCM (4×). The combined organic layers were washed with brine, dried over MgSO.sub.4, filtered and concentrated under vacuum. The crude material was purified by flash chromatography (DCM to DCM/0.6% MeOH) to yield 2-chloro-5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazine (1.57 g, 55%). Light yellow solid. LC-MS: m/z=276.1. [M+H].sup.+.

b) N-(Diphenylmethylene)-5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-amine

(365) ##STR00137##

(366) 2-Chloro-5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazine (1.56 g, 5.66 mmol) was dissolved in Tol (31 ml) under Ar. Diphenylmethaneimine (1.13 g, 1.04 ml, 6.22 mmol), BINAP (352 mg, 566 μmol) and NaOtBu (761 mg, 7.92 mmol) were added. The flask was purged with Ar for 5 min, then [Pd.sub.2(dba).sub.3] (155 mg, 170 μmol) was added. The reaction was stirred 24 h under Ar at 115° C. The reaction mixture was diluted in H.sub.2O, extracted with DCM (3×). The combined organic layers were dried with MgSO.sub.4, filtered and concentrated under vacuum.

(367) The crude material was purified by flash chromatography (DCM to DCM/0.4% MeOH) to yield N-(diphenylmethylene)-5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-amine (1.87 g, 75% yield). Yellow solid. LC-MS: m/z=421.3[M+H].sup.+.

c) 5-(4-(Pyridin-2-yl)piperazin-1-yl)pyrazin-2-amine

(368) ##STR00138##

(369) N-(Diphenylmethylene)-5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-amine (1.87 g, 4.44 mmol) was dissolved in MeOH (85 ml). Hydroxylammonium chloride (617 mg, 8.87 mmol) and NaOAc trihydrate (1.21 g, 8.87 mmol) were added. The reaction was stirred for 30 min at rt. The reaction mixture was concentrated under vacuum. The crude material was purified by flash chromatography (DCM to 98:2 DCM:MeOH to remove benzophenone oxime, then to 15% MeOH in DCM). 5-(4-(Pyridin-2-yl)piperazin-1-yl)pyrazin-2-amine (1.08 g, 95%) was isolated as light brown solid. LC-MS: m/z=257.2 [M+H].sup.+.

d) 2-Fluoro-4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide

(370) 2-Fluoro-4-methoxybenzoic acid (39.8 mg, 234 μmol) was dissolved in DMF (707 μl). HATU (107 mg, 281 μmol) and DIPEA (60.5 mg, 81.8 μl, 468 μmol) were added and the reaction mixture was stirred at rt for 30 min. 5-(4-(Pyridin-2-yl)piperazin-1-yl)pyrazin-2-amine (60 mg, 234 μmol) was added. The solution was stirred 2 h at rt. The solution was diluted in 0.1 M citric acid, then extracted with two portions DCM. The combined organic layers were washed with brine, dried with MgSO.sub.4, filtered and concentrated under vacuum. The crude material was purified by flash chromatography (0% to 20% 98:2 DCM:MeOH in DCM) to yield 2-fluoro-4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide (12 mg, 12%) as off-white solid. LC-MS: m/z=409.2 [M+H].sup.+.

Example 85

4-Methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide

(371) ##STR00139##

(372) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide (Example 84, step d) from 4-methoxybenzoic acid (35.6 mg, 234 μmol) and 5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-amine (Intermediate 84.c) (60 mg, 234 μmol). Yield 67 mg (70%). White solid. LC-MS: m/z=391.2 [M+H].sup.+.

Example 86

4-(Dimethylamino)-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide

(373) ##STR00140##

(374) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide (Example 84, step d) from 4-(dimethylamino)benzoic acid (38.4 mg, 234 μmol) and 5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-amine (Intermediate 84 c) (60 mg, 234 μmol). Yield 15 mg (15%). Light brown solid. LC-MS: m/z=404.2 [M+H].sup.+.

Example 87

4-(4-Methylpiperazin-1-yl)-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide

(375) ##STR00141##

(376) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide (Example 84, step d) from 4-(4-methylpiperazin-1-yl)benzoic acid (51.6 mg, 234 μmol) and 5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-amine (Intermediate 84.c) (60 mg, 234 μmol). Yield 43 mg (38%). Brown solid. LC-MS: m/z=459.2 [M+H].sup.+.

Example 88

4-Morpholino-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide

(377) ##STR00142##

(378) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide (Example 84, step d) from 4-morpholinobenzoic acid (48.5 mg, 234 μmol) and 5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-amine (Intermediate 84.c) (60 mg, 234 μmol). Yield 55 mg (50%). Off-white solid. LC-MS: m/z=446.2 [M+H].sup.+.

Example 89

4-Methyl-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide

(379) ##STR00143##

(380) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide (Example 84, step d) from 4-methylbenzoic acid (31.9 mg, 234 μmol) and 5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-amine (Intermediate 84.c) (60 mg, 234 μmol). Yield 73 mg (79%). Off-white solid. LC-MS: m/z=375.2 [M+H].sup.+.

Example 90

5-Methyl-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)picolinamide

(381) ##STR00144##

(382) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)benzamide (Example 84, step d) from 5-methylpicolinic acid (32.1 mg, 234 μmol) and 5-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-amine (Intermediate 84.c) (60 mg, 234 μmol). Yield 20 mg (22%). Off-white solid. LC-MS: m/z=376.2 [M+H].sup.+.

Example 91

N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-6-methoxypicolinamide

(383) ##STR00145##

(384) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-3-carbonitrile (Intermediate 50.a) (60 mg, 215 μmol) and 6-methoxypicolinic acid (32.9 mg, 215 μmol). Yield 38 mg (41%). Light brown solid. LC-MS: m/z=415.0 [M+H].sup.+.

Example 92

N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-4-morpholinobenzamide

(385) ##STR00146##

(386) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(4-aminophenyl)piperazin-1-yl)benzonitrile (Intermediate 57.a) (60 mg, 216 μmol) and 4-morpholinobenzoic acid (44.7 mg, 216 μmol). 19 mg (18%). White solid. LC-MS: m/z=468.2 [M+H].sup.+.

Example 93

N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-6-methoxypicolinamide

(387) ##STR00147##

(388) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(4-aminophenyl)piperazin-1-yl)benzonitrile (Intermediate 57.a) (60 mg, 216 μmol) and 6-methoxypicolinic acid (33 mg, 216 μmol). 61 mg (65%). Off-white solid. LC-MS: m/z=414.2 [M+H].sup.+.

Example 94

4-Morpholino-N-(4-(4-(thiophen-2-yl)piperazin-1-yl)phenyl)benzamide

(389) ##STR00148##

(390) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(thiophen-2-yl)piperazin-1-yl)aniline (Intermediate 66.a) (60 mg, 231 μmol) and 4-morpholinobenzoic acid (47.9 mg, 231 μmol). 67 mg (61%). Light brown solid. LC-MS: m/z=449.2 [M+H].sup.+.

Example 95

N-(5-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)pyridin-2-yl)-4-methoxybenzamide

(391) ##STR00149##

a) 6-(4-(6-Nitropyridin-3-yl)piperazin-1-yl)nicotinonitrile

(392) ##STR00150##

(393) 6-(Piperazin-1-yl)nicotinonitrile (331 mg, 1.76 mmol) was dissolved in DMSO (1.25 ml). K.sub.2CO.sub.3 (365 mg, 2.64 mmol) and 5-fluoro-2-nitropyridine (250 mg, 1.76 mmol) were added and the solution was stirred 25 min at 90° C. The solution was diluted in H.sub.2O and extracted with DCM. The combined organic layers were washed with brine, dried over MgSO.sub.4, filtered and concentrated under vacuum. The crude product was purified by flash-column chromatography (DCM to 5% MeOH in DCM) to yield 6-(4-(6-nitropyridin-3-yl)piperazin-1-yl)nicotinonitrile (358 mg, 62%). LC-MS: m/z=311.1 [M+H].sup.+.

b) 6-(4-(6-Aminopyridin-3-yl)piperazin-1-yl)nicotinonitrile

(394) ##STR00151##

(395) 6-(4-(6-Nitropyridin-3-yl)piperazin-1-yl)nicotinonitrile (356 mg, 1.09 mmol) was dissolved in EtOH (15 ml) and the solution was placed under Ar. Pd/C 10% (127 mg, 1.09 mmol) was added, and the reaction was stirred at rt under H.sub.2 for 80 min. The reaction mixture was filtered over Celite and washed with EtOH and 9:1 DCM:MeOH, then concentrated under vacuum to yield 6-(4-(6-aminopyridin-3-yl)piperazin-1-yl)nicotinonitrile (319 mg, 99%) as yellow solid. LC-MS: m/z=281.2 [M+H].sup.+.

c) N-(5-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)pyridin-2-yl)-4-methoxybenzamide

(396) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 6-(4-(6-aminopyridin-3-yl)piperazin-1-yl)nicotinonitrile (60 mg, 214 μmol) and 4-methoxybenzoic acid (32.6 mg, 214 μmol). 56 mg (60%). Off-white solid. LC-MS: m/z=415.2 [M+H].sup.+.

Example 96

N-(5-(4-(4-Cyanophenyl)piperazin-1-yl)pyridin-2-yl)-4-methoxybenzamide

(397) ##STR00152##

a) 4-(4-(6-Nitropyridin-3-yl)piperazin-1-yl)benzonitrile

(398) ##STR00153##

(399) 4-(Piperazin-1-yl)benzonitrile (329 mg, 1.76 mmol) was dissolved in DMSO (1.25 ml).

(400) K.sub.2CO.sub.3 (365 mg, 2.64 mmol) and 5-fluoro-2-nitropyridine (250 mg, 1.76 mmol) were added and the solution was stirred 15 min at 90° C. The solution was diluted in H.sub.2O and extracted with DCM. The combined organic layers were washed with brine, dried over MgSO.sub.4, filtered and concentrated under vacuum. The crude product was purified by flash chromatography (DCM to 5% MeOH in DCM) to yield 4-(4-(6-nitropyridin-3-yl)piperazin-1-yl)benzonitrile (448 mg, 78.2%) as yellow solid. LC-MS: m/z=310.2 [M+H].sup.+.

b) 4-(4-(6-Aminopyridin-3-yl)piperazin-1-yl)benzonitrile

(401) ##STR00154##

(402) 4-(4-(6-Nitropyridin-3-yl)piperazin-1-yl)benzonitrile (445 mg, 1.44 mmol) was dissolved in EtOH (20 ml) and the solution was placed under Ar. Pd/C 10% (159 mg, 1.44 mmol) was added, and the reaction was stirred at rt under H.sub.2 for 2 h. The reaction mixture was filtered over Celite and washed with EtOH and 4:1 DCM:MeOH, then concentrated under vacuum to yield 4-(4-(6-aminopyridin-3-yl)piperazin-1-yl)benzonitrile (414 mg, 62%; 60% purity) still containing starting material. This material was used as such in the following step. LC-MS: m/z=280.2 [M+H].sup.+.

c) N-(5-(4-(4-Cyanophenyl)piperazin-1-yl)pyridin-2-yl)-4-methoxybenzamide

(403) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(6-aminopyridin-3-yl)piperazin-1-yl)benzonitrile (60 mg, 215 μmol) and 4-methoxybenzoic acid (32.7 mg, 215 μmol). Yield 25 mg (27%). White solid. LC-MS: m/z=414.2 [M+H].sup.+.

Example 97

N-(2-(4-(4-Cyanophenyl)piperazin-1-yl)pyrimidin-5-yl)-4-methoxybenzamide

(404) ##STR00155##

a) 4-(4-(5-Nitropyrimidin-2-yl)piperazin-1-yl)benzonitrile

(405) ##STR00156##

(406) 2-Chloro-5-nitropyrimidine (270 mg, 1.69 mmol) was dissolved in THF (60 ml) and 4-(piperazin-1-yl)benzonitrile (317 mg, 1.69 mmol) was added. The reaction mixture turned immediately yellow. The reaction mixture was concentrated under vacuum. The crude was diluted in H.sub.2O and extracted with EtOAc and DCM. The combined organic layers were dried with MgSO.sub.4 and concentrated under vacuum. The crude product was purified with flash chromatography (silica gel, 120 g, 0% to 5% MeOH in DCM) to yield 4-(4-(5-nitropyrimidin-2-yl)piperazin-1-yl)benzonitrile (150 mg, 27% yield) as an orange solid. LC-MS: m/z=311.1 [M+H].sup.+.

b) 4-(4-(5-Aminopyrimidin-2-yl)piperazin-1-yl)benzonitrile

(407) ##STR00157##

(408) 4-(4-(5-Nitropyrimidin-2-yl)piperazin-1-yl)benzonitrile (150 mg, 483 μmol) was dissolved in EtOH (6 ml) and the solution was placed under Ar. Pd/C 10% (53.5 mg, 483 μmol) was added and the reaction was stirred 80 min under H.sub.2 at rt. The reaction mixture was filtered over Celite and washed with EtOH and 9:1 DCM:MeOH, then concentrated under vacuum to yield 4-(4-(5-aminopyrimidin-2-yl)piperazin-1-yl)benzonitrile (110 mg, 69%). LCMS: m/z=281.1 [M+H].sup.+.

c) N-(2-(4-(4-Cyanophenyl)piperazin-1-yl)pyrimidin-5-yl)-4-methoxybenzamide

(409) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 4-(4-(5-aminopyrimidin-2-yl)piperazin-1-yl)benzonitrile (35 mg, 125 μmol) and 4-methoxybenzoic acid (19 mg, 125 μmol). Yield 20 mg (37%). Off-white solid. LC-MS: m/z=415.2 [M+H].sup.+.

Example 98

N-(2-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)-4-methoxybenzamide

(410) ##STR00158##

a) 6-(4-(5-Nitropyrimidin-2-yl)piperazin-1-yl)nicotinonitrile

(411) ##STR00159##

(412) 2-Chloro-5-nitropyrimidine (270 mg, 1.69 mmol) was dissolved in THF (60 ml) and 6-(piperazin-1-yl)nicotinonitrile (319 mg, 1.69 mmol) was added. The reaction mixture turned immediately yellow. The reaction mixture was concentrated under vacuum. The crude was diluted in H.sub.2O and extracted with EtOAc and DCM. The combined organic layers were dried with MgSO.sub.4 and concentrated under vacuum. The crude product was purified with flash chromatography (silica gel, 120 g, 0% to 5% MeOH in DCM) to yield 6-(4-(5-nitropyrimidin-2-yl)piperazin-1-yl)nicotinonitrile (246 mg, 44% yield) as an orange solid. LC-MS: m/z=312.1 [M+H].sup.+.

b) 6-(4-(5-Aminopyrimidin-2-yl)piperazin-1-yl)nicotinonitrile

(413) ##STR00160##

(414) 6-(4-(5-Nitropyrimidin-2-yl)piperazin-1-yl)nicotinonitrile (270 mg, 867 μmol) was dissolved in EtOH (11 ml) and the solution was placed under Ar. Pd/C 10% (96.3 mg, 867 μmol) was added and the reaction was stirred overnight under H.sub.2 at rt. The reaction mixture was filtered over Celite and washed with EtOH and 9:1 DCM:MeOH, then concentrated under vacuum to yield 6-(4-(5-aminopyrimidin-2-yl)piperazin-1-yl)nicotinonitrile (157 mg, 58%) as an off-white solid. LC-MS: m/z=282.2 [M+H].sup.+.

c) N-(2-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)-4-methoxybenzamide

(415) The title compound was prepared in analogy to 2-fluoro-4-methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 1, step c) from 6-(4-(5-aminopyrimidin-2-yl)piperazin-1-yl)nicotinonitrile (50 mg, 178 μmol) and 4-methoxybenzoic acid (27 mg, 178 μmol). Yield 45 mg (58%). White solid. LC-MS: m/z=416.2 [M+H].sup.+.

Example 99

N-(2-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)-4-morpholinobenzamide

(416) ##STR00161##

(417) The title compound was prepared in analogy to N-(2-(4-(5-cyanopyridin-2-yl)piperazin-1-yl)pyrimidin-5-yl)-4-methoxybenzamide (Example 98, step c) from 6-(4-(5-aminopyrimidin-2-yl)piperazin-1-yl)nicotinonitrile (Intermediate 98.b) (50 mg, 178 μmol) and 4-morpholinobenzoic acid (36.8 mg, 178 μmol). 15 mg (17%). Off-white solid. LC-MS: m/z=471.2 [M+H].sup.+.

Example 100

N-[4-[4-(6-Cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide

(418) ##STR00162##

a) 6-[4-(4-Nitrophenyl)piperazin-1-yl]pyridine-2-carbonitrile

(419) ##STR00163##

(420) To a solution under N.sub.2 of 6-(piperazin-1-yl)pyridine-2-carbonitrile (750 mg, 3.98 mmol) in DMF (5 ml) was added K.sub.2CO.sub.3 (1.38 mg, 4.38 mmol) and the mixture was stirred at 25° C. for 30 min. After that 4-fluoronitrobenzene (618 mg, 4.38 mmol) was added and the reaction mixture was stirred for 16 h at 25° C. After total consumption of starting materials (monitored by TLC) the reaction mixture was poured into H.sub.2O (50 ml) and extracted with EtOAc (3×100 ml). The combined organic phases were dried over Na.sub.2SO.sub.4 and concentrated under vacuum. The resulting crude was purified by flash chromatography (40% EtOAc/Hexane) to get 6-[4-(4-nitrophenyl)piperazin-1-yl]pyridine-2-carbonitrile (760 mg, 62%) as yellow solid.

b) 6-[4-(4-Aminophenyl)piperazin-1-yl]pyridine-2-carbonitrile

(421) ##STR00164##

(422) To a solution of 6-[4-(4-nitrophenyl)piperazin-1-yl]pyridine-2-carbonitrile (750 mg, 2.43 mmol) in EtOH (10 ml) was added Raney-Ni (50% in H.sub.2O) (2.5 ml). N.sub.2H.sub.4.H.sub.2O (1.1 ml, 24.2 mmol) was added over a 15 min period. The reaction mixture was then heated to 45° C. for 1 h. Raney-Ni was filtered off, washed with EtOH and the filtrate concentrated under vacuum. The resulting crude product was purified by flash chromatography (amine modified silica gel, 60-80% EtOAc/Hexane) to get 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-2-carbonitrile (580 mg, 86%) as grey solid. LC-MS: m/z=280.2 [M+H].sup.+.

c) N-[4-[4-(6-Cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide

(423) To a solution of 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-2-carbonitrile (250 mg, 0.75 mmol) in THF (2.5 ml) cooled with an ice/H.sub.2O bath were added Et.sub.3N (0.2 ml, 1.5 mmol) and 4-methoxybenzoyl chloride (0.1 ml, 0.75 mmol). The reaction mixture was stirred 1 h at 0° C. The reaction mixture was diluted with H.sub.2O (20 ml) and extracted with EtOAc (2×50 ml). The combined organic layers were dried over Na.sub.2SO.sub.4 and concentrated. The resulting crude product was purified by flash chromatography to get the title compound (135 mg, 43%) as off-white solid. LC-MS: m/z=414.1 [M+H].sup.+.

Example 101

4-Methoxy-N-[4-(4-phenylpiperazin-1-yl)phenyl]benzamide

(424) ##STR00165##

a) 1-(4-Nitrophenyl)-4-phenylpiperazine

(425) ##STR00166##

(426) The title compound was prepared in analogy to 6-[4-(4-nitrophenyl)piperazin-1-yl]pyridine-2-carbonitrile (Intermediate 100.a) from 1-phenylpiperazine (500 mg, 3.08 mmol) and 1-fluoro-4-nitrobenzene (478 mg, 3.39 mmol). Crude yield 500 mg. Yellow solid. This material was used without any further purification in the next step.

b) 4-(4-Phenylpiperazin-1-yl)aniline

(427) ##STR00167##

(428) The title compound was prepared in analogy to 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-2-carbonitrile (Intermediate 100.b) from 1-(4-nitrophenyl)-4-phenylpiperazine (500 mg, 1.77 mmol). Yield 405 mg (90%). Grey solid. LC-MS: m/z=253.9 [M+H].sup.+.

c) 4-Methoxy-N-[4-(4-phenylpiperazin-1-yl)phenyl]benzamide

(429) The title compound was prepared in analogy to N-[4-[4-(6-cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide (Example 100, step c) from 4-(4-phenylpiperazin-1-yl)aniline (100 mg, 0.39 mmol) and 4-methoxybenzoyl chloride (0.05 ml, 0.39 mmol). Yield 55 mg (36%). Off-white solid. LC-MS: m/z=388.3 [M+H].sup.+.

Example 102

4-Methoxy-N-[4-[4-(4-methyl-2-pyridyl)piperazin-1-yl]phenyl]benzamide

(430) ##STR00168##

a) 1-(4-Methylpyridin-2-yl)-4-(4-nitrophenyl)piperazine

(431) ##STR00169##

(432) The title compound was prepared in analogy to 6-[4-(4-nitrophenyl)piperazin-1-yl]pyridine-2-carbonitrile (Intermediate 100.a) from 1-(4-methylpyridin-2-yl)piperazine (500 mg, 2.82 mmol) and 1-fluoro-4-nitrobenzene (438 mg, 3.10 mmol). Yield 330 mg (39%). Yellow solid. LC-MS: m/z=299.1 [M+H].sup.+.

b) 4-[4-(4-Methylpyridin-2-yl)piperazin-1-yl]aniline

(433) ##STR00170##

(434) The title compound was prepared in analogy to 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-2-carbonitrile (Intermediate 100.b) from 1-(4-methylpyridin-2-yl)-4-(4-nitrophenyl)piperazine (500 mg, 1.68 mmol). Yield 360 mg (80%). Brown sticky solid. LC-MS: m/z=268.9 [M+H].sup.+.

c) 4-Methoxy-N-[4-[4-(4-methyl-2-pyridyl)piperazin-1-yl]phenyl]benzamide

(435) To a solution of 4-methoxybenzoic acid (100 mg, 0.66 mmol) in THF (5 ml) were added DIPEA (0.43 ml, 2.63 mmol), T3P (50% sol in EA) (1 ml, 1.64 mmol) and 4-[4-(4-methylpyridin-2-yl)piperazin-1-yl]aniline (176 mg, 0.66 mmol). Then the reaction mixture was stirred at 25° C. for 16 h. The reaction mixture was poured into H.sub.2O (20 ml) and extracted with EtOAc (2×50 ml). The combined organic phases were dried over Na.sub.2SO.sub.4 and solvents were evaporated. The resulting crude material was purified by flash chromatography (5% MeOH/DCM) to get the product (26 mg, 10%) as off-white solid. LC-MS: m/z=403.3 [M+H].sup.+.

Example 103

N-[4-[4-(3-Cyanophenyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide

(436) ##STR00171##

a) 3-[4-(4-Nitrophenyl)piperazin-1-yl]benzonitrile

(437) ##STR00172##

(438) The title compound was prepared in analogy to 6-[4-(4-nitrophenyl)piperazin-1-yl]pyridine-2-carbonitrile (Intermediate 100.a) from 3-(piperazin-1-yl)benzonitrile (400 mg, 1.66 mmol) and 1-fluoro-4-nitrobenzene (258 mg, 1.83 mmol). Yield 410 mg (80%). Yellow solid.

b) 3-[4-(4-Aminophenyl)piperazin-1-yl]benzonitrile

(439) ##STR00173##

(440) 3-[4-(4-Nitrophenyl)piperazin-1-yl]benzonitrile (50 mg, 0.16 mmol) and SnCl.sub.2.2H.sub.2O (366 mg, 1.62 mmol) were suspended in EtOH (2.5 ml) and heated to 70° C. for 20 h. EtOH was evaporated and the remaining mixture was diluted with H.sub.2O (10 ml), neutralized with aq. NaHCO.sub.3 solution and extracted with EtOAc (2×30 ml). The combined organic layers were dried over Na.sub.2SO.sub.4 and concentrated to give 3-[4-(4-aminophenyl)piperazin-1-yl]benzonitrile (40 mg, 89%) as brown solid. This material was used with no further purification in the following. LC-MS: m/z=278.9 [M+H].sup.+.

c) N-[4-[4-(3-Cyanophenyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide

(441) The title compound was prepared in analogy to N-[4-[4-(6-cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide (Example 100.c) from 3-[4-(4-aminophenyl)piperazin-1-yl]benzonitrile (40 mg, 0.14 mmol) and 4-methoxybenzoyl chloride (0.02 ml, 0.14 mmol). Yield 45 mg (76%). Off-white solid. LC-MS: m/z=413.3 [M+H].sup.+.

Example 104

N-[4-[4-(3-Fluorophenyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide

(442) ##STR00174##

a) 1-(3-Fluorophenyl)-4-(4-nitrophenyl)piperazine

(443) ##STR00175##

(444) The title compound was prepared in analogy to 6-[4-(4-nitrophenyl)piperazin-1-yl]pyridine-2-carbonitrile (Intermediate 100.a) from 1-(3-fluorophenyl)piperazine (500 mg, 2.77 mmol) and 1-fluoro-4-nitrobenzene (430 mg, 3.05 mmol). Yield 410 mg (80%). Yellow solid. LC-MS: m/z=302.0 [M+H].sup.+.

b) 4-[4-(3-Fluorophenyl)piperazin-1-yl]aniline

(445) ##STR00176##

(446) The title compound was prepared in analogy to 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-2-carbonitrile (Intermediate 100.b) from 1-(3-fluorophenyl)-4-(4-nitrophenyl)piperazine (500 mg, 1.68 mmol). Yield 360 mg (80%). Off-white solid. LC-MS: m/z=272.0 [M+H].sup.+.

c) N-[4-[4-(3-Fluorophenyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide

(447) The title compound was prepared in analogy to 4-methoxy-N-[4-[4-(4-methyl-2-pyridyl)piperazin-1-yl]phenyl]benzamide (Example 102, step c) from 4-[4-(3-fluoro-phenyl)piperazin-1-yl]aniline (178 mg, 0.66 mmol) and 4-methoxybenzoic acid (100 mg, 0.66 mmol). Yield 55 mg (21%). White solid. LC-MS: m/z=406.3 [M+H].sup.+.

Example 105

N-[4-[4-(4-Fluorophenyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide

(448) ##STR00177##

a) 1-(4-Fluorophenyl)-4-(4-nitrophenyl)piperazine

(449) ##STR00178##

(450) The title compound was prepared in analogy to 6-[4-(4-nitrophenyl)piperazin-1-yl]pyridine-2-carbonitrile (Intermediate 100.a) from 1-(4-fluorophenyl)piperazine (500 mg, 2.77 mmol) and 1-fluoro-4-nitrobenzene (430 mg, 3.05 mmol). Yield 540 mg (65%). Yellow solid. LC-MS: m/z=302.2 [M+H].sup.+.

b) 4-[4-(4-Fluorophenyl)piperazin-1-yl]aniline

(451) ##STR00179##

(452) The title compound was prepared in analogy to 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-2-carbonitrile (Intermediate 100.b) from 1-(4-fluorophenyl)-4-(4-nitrophenyl)piperazine (500 mg, 1.68 mmol). Yield 380 mg (84%). Off-white solid. LC-MS: m/z=217.9 [M+H].sup.+.

c) N-[4-[4-(4-Fluorophenyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide

(453) The title compound was prepared in analogy to 4-methoxy-N-[4-[4-(4-methyl-2-pyridyl)piperazin-1-yl]phenyl]benzamide (Example 102.c) from 4-[4-(4-fluorophenyl)piperazin-1-yl]aniline (178 mg, 0.66 mmol) and 4-methoxybenzoic acid (100 mg, 0.66 mmol). Yield 27 mg (10%). Off-white solid. LC-MS: m/z=406.2 [M+H].sup.+.

Example 106

N-[3-Fluoro-4-[4-(2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide

(454) ##STR00180##

(455) To a solution of 3-fluoro-4-[4-(2-pyridyl)piperazin-1-yl]aniline (CAS Nr. 202133-31-1) (200 mg, 0.730 mmol) in THF (10 ml) at 0° C. under N.sub.2 was added Et.sub.3N (0.2 ml, 1.51 mmol) and 4-methoxybenzoyl chloride (0.1 ml, 0.73 mmol). The mixture was stirred 1 h at 0° C. The reaction mixture was diluted with H.sub.2O and extracted with EtOAc (2×50 ml) and the organic layers were washed with brine, dried over Na.sub.2SO.sub.4 and concentrated under reduced pressure. The resulting crude product was purified by flash chromatography to get N-[3-fluoro-4-[4-(2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide (270 mg, 89%) as off-white solid. LC-MS: m/z=407.3 [M+H].sup.+.

Example 107

N-[4-[4-(5-Cyano-2-pyridyl)piperazin-1-yl]-3-fluoro-phenyl]-4-methoxy-benzamide

(456) ##STR00181##

a) 6-[4-(4-Amino-2-fluoro-phenyl)piperazin-1-yl]pyridine-3-carbonitrile

(457) ##STR00182##

(458) 6-[4-(2-Fluoro-4-nitro-phenyl)piperazin-1-yl]pyridine-3-carbonitrile (400 mg, 1.22 mmol) and SnCl.sub.2.2H.sub.2O (2.76 g, 12.2 mmol) were suspended in EtOH (10 ml) and heated to 70° C. for 16 h. EtOH was evaporated and the residue was diluted with H.sub.2O, neutralized with aq. NaHCO.sub.3 solution and extracted with DCM (2×100 ml). The combined organic layers were dried over Na.sub.2SO.sub.4 and concentrated to give 6-[4-(4-amino-2-fluoro-phenyl)piperazin-1-yl]pyridine-3-carbonitrile (270 mg, 74%) as off-white solid. This material was used in the following step without further purification. LC-MS: m/z=298.3 [M+H].sup.+.

b) N-[4-[4-(5-Cyano-2-pyridyl)piperazin-1-yl]-3-fluoro-phenyl]-4-methoxy-benzamide

(459) The title compound was prepared in analogy to N-[3-fluoro-4-[4-(2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide (Example 106) from 6-[4-(4-amino-2-fluoro-phenyl)piperazin-1-yl]pyridine-3-carbonitrile (200 mg, 0.67 mmol) and 4-methoxybenzoyl chloride (0.09 ml, 0.67 mmol). Yield 18 mg (6%). White solid. LC-MS: m/z=432.2 [M+H].sup.+.

Example 108

N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-hydroxybenzamide

(460) ##STR00183##

a) [4-[[4-[4-(5-Cyano-2-pyridyl)piperazin-1-yl]phenyl] carbamoyl]phenyl] acetate

(461) ##STR00184##

(462) To a solution of 4-acetoxybenzoic acid (1.29 g, 7.16 mmol) in DCM (60 ml) were added oxalyl chloride (1.36 g, 940 μl, 10.7 mmol) and DMF (26.2 mg, 27.7 μl, 358 μmol) and the mixture stirred at 20-25° C. for 1.5 h. The reaction mixture was concentrated under vacuum. The crude product was dissolved in DCM (30 ml) and added to a solution of 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-3-carbonitrile (Intermediate 50.a) (2.0 g, 7.16 mmol) and DIPEA (3.7 g, 5.0 ml, 28.6 mmol) in DCM (60 ml). The light brown suspension was stirred at 20-25° C. for 30 min. Then MeOH (6 ml) was added to quench the reaction. The suspension was stirred for 1 h and filtered. The cake was washed with DCM (10 ml) and dried on the filter for 2 min. Then the cake was washed with H.sub.2O (25 ml) and finally dried under vacuum at 40° C. to obtain the desired product (2.91 g, 92%) as colorless crystals. LC MS m/z=442.3 [M+H].sup.+.

b) N-[4-[4-(5-Cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-hydroxy-benzamide

(463) To a suspension of 4-((4-(4-(5-cyanopyridin-2-yl)piperazin-1-yl)phenyl)carbamoyl)phenyl acetate (2.8 g, 6.34 mmol) in MeOH (84 ml) was added NaOH 1M in H.sub.2O (25.4 ml, 25.4 mmol), and the suspension was stirred for 1 h. Most of MeOH was removed under vacuum. Then HCl 1M in H.sub.2O (25.4 ml, 25.4 mmol) was added to reach pH 4-5. The resulting suspension was filtered, the cake washed with H.sub.2O (25 ml) and then dried under vacuum at 40° C. to obtain the desired product (2.48 g, 98%) as white crystals. LC-MS: m/z=400.3 [M+H].sup.+.

Example 109

4-Methoxy-N-[4-[4-(p-tolyl)piperazin-1-yl]phenyl]benzamide

(464) ##STR00185##

(465) The title compound was prepared in analogy to N-[4-[4-(6-cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide (Example 100, step c) from 4-[4-(p-tolyl)piperazin-1-yl]aniline (CAS Nr. 68944-99-0) (100 mg, 0.370 mmol) and 4-methoxybenzoyl chloride (0.06 ml, 0.41 mmol). Yield 46 mg (29%). Off-white solid. LC-MS: m/z=402.3 [M+H].sup.+.

Example 110

4-Methoxy-N-[4-[4-(4-methoxyphenyl)piperazin-1-yl]phenyl]benzamide

(466) ##STR00186##

(467) The title compound was prepared in analogy to N-[4-[4-(6-cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide (Example 100, step c) from 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline (CAS Nr. 74852-62-3) (75.0 mg, 0.260 mmol) and 4-methoxybenzoyl chloride (0.04 ml, 0.290 mmol). Yield 80 mg (69%). White solid. LC-MS: m/z=418.2 [M+H].sup.+.

Example 111

4-Methoxy-N-[4-[4-(4-methylsulfonylphenyl)piperazin-1-yl]phenyl]benzamide

(468) ##STR00187##

a) 1-(4-Methylsulfonylphenyl)-4-(4-nitrophenyl)piperazine

(469) ##STR00188##

(470) The title compound was prepared in analogy to 6-[4-(4-nitrophenyl)piperazin-1-yl]pyridine-2-carbonitrile (Intermediate 100.a) from 1-(4-methylsulfonylphenyl)piperazine (730.0 mg, 3.04 mmol) and 1-fluoro-4-nitrobenzene (471 mg, 3.34 mmol). Yield 520 mg (43%). Yellow solid.

b) 4-[4-(4-Methylsulfonylphenyl)piperazin-1-yl]aniline

(471) ##STR00189##

(472) 1-(4-Methylsulfonylphenyl)-4-(4-nitrophenyl)piperazine (500 mg, 1.38 mmol) and SnCl.sub.2.2H.sub.2O (3.12 g, 13.8 mmol) were suspended in EtOH (10 ml) and heated to 70° C. for 16 h. EtOH was evaporated under reduced pressure and the residue was diluted with H.sub.2O, neutralised with aq. NaHCO.sub.3 solution and extracted with DCM (2×100 ml). The combined organic layers were dried over Na.sub.2SO.sub.4 and concentrated to give 4-[4-(4-methylsulfonylphenyl)piperazin-1-yl]aniline (220 mg 46%) as off-white solid. This material was used without further purification in the next step. LC-MS: m/z=232.2 [M+H].sup.+.

c) 4-Methoxy-N-[4-[4-(4-methylsulfonylphenyl)piperazin-1-yl]phenyl]benzamide

(473) The title compound was prepared in analogy to N-[4-[4-(6-cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide (Example 100.c) from 4-[4-(4-methylsulfonylphenyl)piperazin-1-yl]aniline (100 mg, 0.300 mmol) and 4-methoxybenzoyl chloride (0.04 ml, 0.330 mmol). Yield 57 mg (39%). White solid. LC-MS: m/z=466.3 [M+H].sup.+.

Example 112

N-[4-[4-(4-Cyanophenyl)piperazin-1-yl]-3-methyl-phenyl]-4-methoxy-benzamide

(474) ##STR00190##

a) 4-[4-(2-Methyl-4-nitro-phenyl)piperazin-1-yl]benzonitrile

(475) ##STR00191##

(476) To a solution under N.sub.2 of 1-(4-cyanophenyl)piperazine (543 mg, 2.9 mmol) in DMF (10 ml) was added K.sub.2CO.sub.3 (672 mg, 4.83 mmol) and the mixture was stirred at 25° C. for 5 min. After that 2-fluoro-5-nitrotoluene (300 mg, 1.93 mmol) was added. The reaction vessel was sealed and the mixture was stirred 16 h at 100° C. After cooling to 25° C., the reaction mixture was diluted with H.sub.2O (30 ml) and extracted with EtOAc (2×100 ml). The organic phases were washed with brine, dried over Na.sub.2SO.sub.4 and concentrated under reduced pressure. The crude product was purified by flash chromatography (20% EtOAc/hexane) to get 4-[4-(2-methyl-4-nitro-phenyl)piperazin-1-yl]benzonitrile (440 mg, 63%) as orange solid.

b) 4-[4-(4-Amino-2-methyl-phenyl)piperazin-1-yl]benzonitrile

(477) ##STR00192##

(478) 4-[4-(2-Methyl-4-nitro-phenyl)piperazin-1-yl]benzonitrile (400 mg, 1.24 mmol) and SnCl.sub.2.2H.sub.2O (2.80 g, 12.4 mmol) were suspended in EtOH (10 ml) and heated to 70° C. for 20 h. EtOH was evaporated under reduced pressure and the residue was diluted with H.sub.2O (20 ml), neutralised with aq. NaHCO.sub.3 solution and extracted with DCM (2×100 ml). The combined organic layers were dried over Na.sub.2SO.sub.4 and concentrated to give the title compound (200 mg, 51%) as off-white solid. This material was used without further purification in the next step.

c) N-[4-[4-(4-Cyanophenyl)piperazin-1-yl]-3-methyl-phenyl]-4-methoxy-benzamide

(479) The title compound was prepared in analogy to N-[4-[4-(6-cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide (Example 100, step c) from 4-[4-(4-amino-2-methyl-phenyl)piperazin-1-yl]benzonitrile (200 mg, 0.680 mmol) and 4-methoxybenzoyl chloride (0.1 ml, 0.750 mmol). Yield 75 mg (23%). Off-white solid. LC-MS: m/z=427.3 [M+H].sup.+.

Example 113

N-[4-[4-(5-Cyano-2-pyridyl)piperazin-1-yl]-3-methyl-phenyl]-4-methoxy-benzamide

(480) ##STR00193##

a) 6-[4-(2-Methyl-4-nitro-phenyl)piperazin-1-yl]pyridine-3-carbonitrile

(481) ##STR00194##

(482) The title compound was prepared in analogy to 4-[4-(2-methyl-4-nitro-phenyl)piperazin-1-yl]benzonitrile (Intermediate 112.a) from 6-piperazinonicotinonitrile (546 mg, 2.9 mmol) and 2-fluoro-5-nitrotoluene (300 mg, 1.93 mmol). Yield 229 mg (32%). Yellow solid.

b) 6-[4-(4-Amino-2-methyl-phenyl)piperazin-1-yl]pyridine-3-carbonitrile

(483) ##STR00195##

(484) The title compound was prepared in analogy to 4-[4-(4-amino-2-methyl-phenyl)piperazin-1-yl]benzonitrile (Intermediate 112.b) from 6-[4-(2-methyl-4-nitro-phenyl)piperazin-1-yl]pyridine-3-carbonitrile (200 mg, 0.620 mmol). Yield 160 mg (84%). Off-white solid. LCMS: m/z=311.4 [M+NH4].sup.+.

c) N-[4-[4-(5-Cyano-2-pyridyl)piperazin-1-yl]-3-methyl-phenyl]-4-methoxy-benzamide

(485) The title compound was prepared in analogy to N-[4-[4-(6-cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide (Example 100, step c) from 6-[4-(4-amino-2-methyl-phenyl)piperazin-1-yl]pyridine-3-carbonitrile (160 mg, 0.550 mmol) and 4-methoxybenzoyl chloride (0.08 ml, 0.60 mmol). Yield 120 mg (48%). Off-white solid. LC-MS: m/z=428.3 [M+H].sup.+.

Example 114

N-[4-[4-(4-Cyanophenyl)piperazin-1-yl]phenyl]-2-fluoro-4-methoxy-benzamide

(486) ##STR00196##

(487) To a solution of 4-[4-(4-aminophenyl)piperazin-1-yl]benzonitrile (Intermediate 57.a) (250 mg, 0.900 mmol) in dry THF (10 ml) cooled with an ice/H.sub.2O bath, were added Et.sub.3N (0.29 ml, 2.25 mmol) and 2-fluoro-4-methoxybenzoyl chloride (186 mg, 0.990 mmol). The reaction mixture was stirred 1 h at 0° C. Then the reaction mixture was poured into H.sub.2O (10 ml) and extracted with EtOAc (2×50 ml). The combined organic layers were dried over Na.sub.2SO.sub.4, and concentrated. The resulting crude product was purified by flash chromatography (50% EtOAc/hexane) to get N-[4-[4-(4-cyanophenyl)piperazin-1-yl]phenyl]-2-fluoro-4-methoxy-benzamide (216 mg, 52%) as off-white solid. LC-MS: m/z=431.2 [M+H].sup.+.

Example 115

N-[4-[4-(5-Cyano-2-pyridyl)piperazin-1-yl]phenyl]-2-fluoro-4-methoxy-benzamide

(488) ##STR00197##

(489) The title compound was prepared in analogy to N-[4-[4-(4-cyanophenyl)piperazin-1-yl]phenyl]-2-fluoro-4-methoxy-benzamide (Example 114) from 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-3-carbonitrile (Intermediate 50.a) (200 mg, 0.670 mmol) and 2-fluoro-4-methoxybenzoyl chloride (186 mg, 0.980 mmol). Yield 77 mg (19%). Off-white solid. LCMS: m/z=432.2 [M+H].sup.+.

Example 116

N-[4-[4-(5-Cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-(2-fluoroethoxy)benzamide

(490) ##STR00198##

(491) To a solution of 4-(2-fluoroethoxy)benzoic acid [CAS Nr. 145304-35-4] (150 mg, 0.810 mmol) in DMF (5 ml) were added DIPEA (0.42 ml, 2.44 mmol), EDC HCl (234 mg, 1.22 mmol), HOBt (165 mg, 1.22 mmol) and 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-3-carbonitrile (Intermediate 50.a) (227 mg, 0.810 mmol). The reaction mixture was stirred at 25° C. for 16 h. The reaction mixture was poured into H.sub.2O (20 ml) and extracted with EtOAc (2×50 ml). The combined organic layers were dried over Na.sub.2SO.sub.4 and solvents were evaporated. The resulting crude product was purified by flash chromatography (amine silica gel, 50% EtOAc/Hexane) to get N-[4-[4-(5-cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-(2-fluoroethoxy)benzamide (170 mg, 47%) as off-white solid. LC-MS: m/z=446.3 [M+H].sup.+.

Example 117

N-[4-[4-(4-Cyanophenyl)piperazin-1-yl]phenyl]-4-(2-fluoroethoxy)benzamide

(492) ##STR00199##

(493) The title compound was prepared in analogy to N-[4-[4-(5-cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-(2-fluoroethoxy)benzamide (Example 116) from 4-[4-(4-aminophenyl)piperazin-1-yl]benzonitrile (Intermediate 57.a) (227 mg, 0.810 mmol) and 4-(2-fluoroethoxy)benzoic acid (CAS Nr. 145304-35-4) (150 mg, 0.810 mmol). Yield 70 mg (19%). Light yellow solid. LC-MS: m/z=445.1 [M+H].sup.+.

Example 118

4-(2-Fluoroethoxy)-N-[4-[4-(2-pyridyl)piperazin-1-yl]phenyl]benzamide

(494) ##STR00200##

(495) The title compound was prepared in analogy to N-[4-[4-(5-cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-(2-fluoroethoxy)benzamide (Example 116) from 4-[4-(2-pyridyl)piperazin-1-yl]aniline (Intermediate 1.b) (249 mg, 0.980 mmol) and 4-(2-fluoroethoxy)benzoic acid (CAS Nr. 145304-35-4) (150 mg, 0.810 mmol). Yield 10 mg (3%). Off-white solid. LC-MS: m/z=421.0 [M+H].sup.+.

Example 119

4-(2-Fluoroethoxy)-N-[4-(4-thiazol-2-ylpiperazin-1-yl)phenyl]benzamide

(496) ##STR00201##

(497) The title compound was prepared in analogy to N-[4-[4-(5-cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-(2-fluoroethoxy)benzamide (Example 116) from 4-(4-thiazol-2-ylpiperazin-1-yl)aniline (Intermediate 13.b) (254 mg, 0.980 mmol) and 4-(2-fluoroethoxy)benzoic acid (CAS Nr. 145304-35-4) (150 mg, 0.810 mmol). Yield 76 mg (20%). Light yellow solid. LCMS: m/z=427.2 [M+H].sup.+.

Example 120

4-[2-[2-(2-Fluoroethoxy)ethoxy]ethoxy]-N-[4-(4-thiazol-2-ylpiperazin-1-yl)phenyl]benzamide

(498) ##STR00202##

(499) The title compound was prepared in analogy to N-[4-[4-(5-cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-(2-fluoroethoxy)benzamide (Example 116) from 4-(4-thiazol-2-ylpiperazin-1-yl)aniline (Intermediate 13.b) (115 mg, 0.440 mmol) and 4-[2-[2-(2-fluoroethoxy)ethoxy]ethoxy]benzoic acid (CAS Nr. 1269797-18-3) (100 mg, 0.370 mmol). Yield 105 mg (55%). Off-white solid. LC-MS: m/z=515.2 [M+H].sup.+.

Example 121

N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-(2-(2-fluoroethoxy)ethoxy)benzamide

(500) ##STR00203##

a) 2-(2-Hydroxyethoxy)ethyl 4-methylbenzenesulfonate

(501) ##STR00204##

(502) To a solution of diethyleneglycol (20.0 g, 17.9 ml, 188 mmol) in DCM (200 ml) under argon were added tosyl chloride (53.9 g, 283 mmol) and silver oxide (65.5 g, 283 mmol) and the suspension was cooled to 0-5° C. Then potassium iodide (6.26 g, 37.7 mmol) was added over 10 min in 5 portions. After the addition was completed, the reaction was warmed to 20-25° C. and stirred for 1.5 h. The dark grey suspension was filtered, the cake washed with DCM (100 ml), and the filtrate concentrated under vacuum at 40° C. A yellowish non-transparent emulsion was obtained which was purified by flash chromatography (SiO.sub.2, Hept/EtOAc 5% to 90%) to obtain the desired product (11.6 g, 24%) as a colorless oil. LC-MS: m/z=415.2 [M+H].sup.+.

b) 2-(2-Fluoroethoxy)ethyl 4-methylbenzenesulfonate

(503) ##STR00205##

(504) To a solution of 2-(2-hydroxyethoxy)ethyl 4-methylbenzenesulfonate (7.64 g, 29.3 mmol) in DCM (115 ml) under Ar was added at 0-5° C. diethylaminosulfur trifluoride (14.2 g, 11.6 ml, 88 mmol). The light yellow solution was warmed to 20-25° C. and was stirred for 1 h. The reaction mixture was cooled again to 5-10° C. and quenched with 1M NaHCO.sub.3 (200 ml) and solid NaHCO.sub.3 (11 g) was added to reach pH 7-8. The organic layer was concentrated under vacuum. Due to bad conversion, the crude was dissolved again in DCM (115 ml) under Ar and diethylaminosulfur trifluoride (7.1 g, 5.82 ml, 44 mmol) was added at 0-5° C. The light yellow solution was warmed to 20-25° C. and stirred for 1 h. The reaction mix was cooled again to 5-10° C. and quenched with 1M NaHCO.sub.3 (200 ml), and solid NaHCO.sub.3 (3 g) was added to reach pH 7-8. The organic layer was concentrated under vacuum to obtain the crude product as a yellow oil which was purified by MPLC over silica (eluent: heptane/ethyl acetate) to obtain the desired product (3.4 g, 44%) as a light yellow oil. .sup.1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.56 (s, 1H) 1.90 (t, J=6.18 Hz, 1H) 2.45 (s, 3H) 3.50-3.57 (m, 2H) 3.63-3.74 (m, 4H) 4.16-4.25 (m, 2H) 7.31-7.41 (m, 2H) 7.76-7.85 (m, 2H). LCMS: m/z=261.2 [M−H].sup.−.

c) Methyl 4-[2-(2-fluoroethoxy)ethoxy]benzoate

(505) ##STR00206##

(506) To a solution of 2-(2-fluoroethoxy)ethyl 4-methylbenzenesulfonate (3.4 g, 13 mmol) in DMF (34 ml) were added methyl 4-hydroxybenzoate (1.97 g, 13 mmol,) and Cs.sub.2CO.sub.3 (8.45 g, 25.9 mmol). The yellow suspension was heated to 50° C. for 2 h. The reaction was quenched with H.sub.2O (200 ml) and extracted with EtOAc (3×200 ml). The combined organic layers were dried over Na.sub.2SO.sub.4 and concentrated under vacuum to obtain the crude product as yellow oil. Purification by MPLC over silica (eluent: heptane/ethyl acetate) provided the desired product (2.86, 91%) as colorless oil. LC MS: m/z=243.2 [M+H].sup.+.

d) 4-[2-(2-Fluoroethoxy)ethoxy]benzoic acid

(507) ##STR00207##

(508) To a solution of methyl 4-(2-(2-fluoroethoxy)ethoxy)benzoate (2.86 g, 11.8 mmol) in MeOH (29 ml) was added 2M aq.NaOH (23.6 ml, 47.2 mmol), and the colorless solution was stirred at 20-25° C. for 2 h. Most of MeOH was removed under vacuum. Then 2 M aq. HCl (23.6 ml, 47.2 mmol) was added over 1 min to reach pH 1-2 and an homogenous suspension was formed. The suspension was stirred for 1 h at 20-25° C., filtered, and the cake was washed with H.sub.2O (2×10 ml) and dried under vacuum to obtain the desired product (2.64 g, 98%) as colorless crystals. LC MS: m/z=229.2 [M+H].sup.+.

e) N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-(2-(2-fluoroethoxy)ethoxy)benzamide

(509) To a solution of 4-(2-(2-fluoroethoxy)ethoxy)benzoic acid (833 mg, 3.65 mmol) in DCM (30 ml) were added oxalyl chloride (695 mg, 479 μl, 5.48 mmol) and DMF (13.3 mg, 14.1 μl, 183 μmol) and the mixture was stirred at 20-25° C. for 1.5 h. The reaction mixture was concentrated under vacuum at 40° C. The crude acid chloride was dissolved in DCM (15 ml) and added to a solution of 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-3-carbonitrile (Intermediate 50.a) (1.02 g, 3.65 mmol) and DIPEA (1.89 g, 2.55 ml) in DCM (30 ml). The light yellow, thick suspension was stirred at 20-25° C. for 30 min. Then MeOH (3 ml) was added to quench the reaction. The resulting suspension was stirred for 1 h, filtered, and the cake was washed with DCM (10 ml) and dried on the filter for 2 min. Then the cake was washed with H.sub.2O (25 ml) and finally dried under vacuum at 40° C. to obtain the desired product (1.34 g, 75%) as colorless crystals. LC MS: m/z=490.2 [M+H].sup.+.

Example 122

N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-4-(2-(2-fluoroethoxy)ethoxy)benzamide

(510) ##STR00208##

(511) To a solution of 4-(2-(2-fluoroethoxy)ethoxy)benzoic acid (Intermediate 121.d) (74.3 mg, 326 μmol) in DMF (2 ml) was added at 22° C. HATU (124 mg, 326 μmol) followed by N,N-diisopropylethylamine (80.1 mg, 108 μl, 620 μmol) and the mixture was stirred at 22° C. for 30 min. Then was added 4-(4-(4-aminophenyl)piperazin-1-yl)benzonitrile (Intermediate 57.a) (86.3 mg, 310 μmol) to give after 30 min a brown suspension. After stirring at 22° C. for a total 2 h the mixture was quenched with half-sat. NaHCO.sub.3 (20 ml) and extracted with DCM (4×20 ml). The organic layers were dried and evaporated, and further dried in the HV at 50° C. The crude product was suspended in 6 ml DCM for 3 h. The solid was filtered off, washed with DCM (2×1 ml) and dried in HV to give a first portion of not yet clean product. The filtrate was treated with DCM/MeOH resulting after filtration in a second portion of product. The combined solids and the clear filtrate were purified separately by flash chromatography (silica gel; MeOH in DCM 0% to 4%) to give pure product. Combined yield 91 mg (60%). Off-white solid. LC-MS: m/z=489.5 [M+H].sup.+.

Example 123

N-[4-[4-(4-Cyanophenyl)piperazin-1-yl]phenyl]-4-[2-[2-(2-fluoroethoxy)ethoxy]ethoxy]benzamide

(512) ##STR00209##

(513) The title compound was prepared in analogy to N-[4-[4-(5-cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-(2-fluoroethoxy)benzamide (Example 116) from 4-[4-(4-aminophenyl)piperazin-1-yl]benzonitrile (Intermediate 57.a) (123 mg, 0.440 mmol) and 4-[2-[2-(2-fluoroethoxy)ethoxy]ethoxy]benzoic acid (CAS Nr. 1269797-18-3) (100 mg, 0.370 mmol). Yield 42 mg (21%). Off-white solid. LC-MS: m/z=533.3 [M+H].sup.+.

Example 124

rac-4-(2-((tert-Butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(514) ##STR00210##

a) rac-Methyl 4-(3-fluoro-2-hydroxypropoxy)benzoate

(515) ##STR00211##

(516) To a solution of methyl rac-4-(oxiran-2-ylmethoxy)benzoate (CAS Nr. 5535-03-5) (312 mg, 1.5 mmol) in Tol (3 ml) was added at 22° C. tetra-n-butylammonium fluoride, 1 M in THF (3.3 ml, 3.3 mmol). The mixture was warmed to 80° C. and stirred for 1 h. The mixture was evaporated, quenched with H.sub.2O (6 ml) and set acidic (pH=1-2) by addition of 1 N aq. HCl (3.3 ml). The aqueous mixture was extracted with ethyl acetate (3×10 ml). The organic layers were washed with sat NaCl (2×10 ml), dried and evaporated. The residue was purified by flash chromatography (silica gel, 12 g, EtOAc in heptane 5% to 40% to 100%) to give the title compound (120 mg, 35%) as colorless oil. LC-MS: m/z=229.2 [M+H)].sup.+.

b) rac-Methyl 4-(2-((tert-butyldimethylsilyl)oxy)-3-fluoropropoxy)benzoate

(517) ##STR00212##

(518) To a solution of methyl 4-(3-fluoro-2-hydroxypropoxy)benzoate (100 mg, 438 μmol) in DCM (1.5 ml) was added at 22° C. imidazole (59.7 mg, 876 μmol) followed by DMAP (5.35 mg, 43.8 μmol). Then was added dropwise a solution of TBDMS-Cl (79.3 mg, 526 μmol) in DCM (0.5 ml) and the mixture was stirred at 22° C. for 90 min to give ca. 60% conversion. After 3.5 h further imidazole (89.5 mg, 1.31 mmol) was added followed by a solution of TBDMS-Cl (119 mg, 789 μmol) in DCM (1 ml). The reaction mixture was stirred for 15 min at 22° C. to give complete conversion. The solid was filtered off and washed with DCM (2×2 ml). The filtrate was evaporated, adsorbed on Isolute HM-N and directly purified by flash chromatography (silica gel, 12 g, EtOAc in heptane 5% to 20% to 50%) to give the title compound (113 mg, 75%) as colorless oil. LC-MS: m/z=343.3 [M+H].sup.+.

c) rac-4-(2-((tert-Butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(519) To a solution of 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (58 mg, 228 μmol) in dioxane (2.3 ml) was added at 22° C. trimethylaluminum, 2 M in heptane (114 μl, 228 μmol). The resulting mixture was stirred at 22° C. for 1 h. Then was added a solution of methyl 4-(2-((tert-butyldimethylsilyl)oxy)-3-fluoropropoxy)benzoate (78.1 mg, 228 μmol) in dioxane (0.6 ml) and the reaction was heated to 90° C. and stirred at 90° C. for 1 h to give complete conversion. The mixture was cooled to 22° C., quenched with H.sub.2O (1 ml), diluted with ethyl acetate (3 ml) and evaporated. The residue was treated with H.sub.2O and extracted with EtOAc (3×10 ml). The organic layer was dried and evaporated. The residue (120 mg, 93%) was combined with crude product from a preliminary experiment (14 mg) and purified by flash chromatography (silica gel, 4 g, dissolved in DCM, MeOH in DCM 1% to 2% to 5%) to give the title compound (88 mg, 68%; corrected yield=61%) as a light yellow solid. LC-MS: m/z=565.4 [M+H].sup.+.

Example 125

rac-4-(3-Fluoro-2-hydroxypropoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(520) ##STR00213##

(521) To a solution of 4-(2-((tert-butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 124) (67 mg, 119 μmol) in THF (1.3 ml) was added at 22° C. tetra-n-butylammonium fluoride, 1 M in THF (130 μl, 130 μmol) and the mixture was stirred at 22° C. for 30 min to give complete conversion. The clear light yellow solution was treated dropwise with H.sub.2O (3 ml) to precipitate the product. After stirring for 30 min the solid product was filtered off. The solid was washed with H.sub.2O (2×2 ml) and H.sub.2O/ACN 1:1 (2×1 ml). The solid was dried under high vacuum to give the title compound (40 mg, 75%) as off-white solid. LC-MS: m/z=451.4 [M+H].sup.+.

Example 126

rac-4-(2-((tert-Butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(thiazol-2-yl)piperazin-1-yl)phenyl)benzamide

(522) ##STR00214##

(523) The title compound was prepared in analogy to rac-4-(2-((tert-butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 124, step c) from 4-[4-(1,3-thiazol-2-yl)piperazin-1-yl]aniline (Intermediate 13.b) (78.1 mg, 300 μmol) and rac-methyl 4-(2-((tert-butyldimethylsilyl)oxy)-3-fluoropropoxy)benzoate (Intermediate 124.b) (103 mg, 300 μmol). Yield 81 mg (47%) as a light yellow solid. LC-MS: m/z=571.4 [M+H].sup.+.

Example 127

rac-4-(2-((tert-Butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(4-cyanophenyl)piperazin-1-yl)phenyl)benzamide

(524) ##STR00215##

(525) The title compound was prepared in analogy to rac-4-(2-((tert-butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 124, step c) from 4-(4-(4-aminophenyl)piperazin-1-yl)benzonitrile (Intermediate 57.a) (83.5 mg, 300 μmol) and rac-methyl 4-(2-((tert-butyldimethylsilyl)oxy)-3-fluoropropoxy)benzoate (Intermediate 124.b) (103 mg, 300 μmol). Yield 120 mg (68%). Yellow solid. LC-MS: m/z=589.4 [M+H].sup.+.

Example 128

rac-4-(2-((tert-Butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(4-cyanopyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(526) ##STR00216##

a) 2-[4-(4-Nitrophenyl)piperazin-1-yl]pyridine-4-carbonitrile

(527) ##STR00217##

(528) 2-(Piperazin-1-yl)isonicotinonitrile (500 mg, 2.66 mmol) was combined with DMSO (1.90 ml) to give a light yellow solution. K.sub.2CO.sub.3 (551 mg, 3.98 mmol) and 1-fluoro-4-nitrobenzene (375 mg, 2.66 mmol) were added and the solution was stirred at 90° C. for 1 h. The reaction mixture was diluted with H.sub.2O (50 ml) and extracted with DCM (3×50 ml). The combined organic layers were washed with brine (1×50 ml), dried over MgSO.sub.4 and concentrated under vacuum. The crude product was purified by flash chromatography. (50 g SiO2 cartridge, DCM to DCM/MeOH 98:0.2) to yield the title compound (751 mg, 91%) as yellow solid. LC-MS: m/z=310.1 [M+H].sup.+.

b) 2-[4-(4-Aminophenyl)piperazin-1-yl]pyridine-4-carbonitrile

(529) ##STR00218##

(530) 2-[4-(4-Nitrophenyl)piperazin-1-yl]pyridine-4-carbonitrile (750 mg, 2.42 mmol) was dissolved in EtOH (30 ml) and placed under argon. Pd/C 10% (258 mg, 242 μmol) was added, and the reaction was stirred 4 h under H.sub.2 at rt. The reaction mixture was filtered over Celite. The solids were washed with EtOH and 4:1 DCM:MeOH. The filtrate was concentrated under vacuum and the so obtained crude material was purified by flash chromatography. (70 g SiO2 cartridge, DCM to DCM/MeOH 98:2) to yield the title compound (413 mg, 58%) as an off-white solid. LC-MS: m/z=280.2 [M+H].sup.+.

c) rac-4-(2-((tert-Butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(4-cyanopyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(531) The title compound was prepared in analogy to rac-4-(2-((tert-butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 124, step c) from 2-[4-(4-aminophenyl)piperazin-1-yl]pyridine-4-carbonitrile (83.8 mg, 300 μmol) and rac-methyl 4-(2-((tert-butyldimethylsilyl)oxy)-3-fluoropropoxy)benzoate (Intermediate 124.b) (103 mg, 300 μmol). Yield 149 mg (84%). Light yellow solid. LC-MS: m/z=590.5 [M+H].sup.+.

Example 129

rac-N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-(3-fluoro-2-hydroxypropoxy)benzamide

(532) ##STR00219##

a) 4-(2-((tert-Butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(5-cyanopyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(533) ##STR00220##

(534) The title compound was prepared in analogy to rac-4-(2-((tert-butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 124, step c) from 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-3-carbonitrile (Intermediate 50.a) (83.8 mg, 300 μmol) and rac-methyl 4-(2-((tert-butyldimethylsilyl)oxy)-3-fluoropropoxy)benzoate (Intermediate 124.b) (103 mg, 300 μmol). Yield 109 mg (62%). Yellow solid. LC-MS: m/z=590.4 [M+H].sup.+.

b) rac-N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-(3-fluoro-2-hydroxypropoxy)benzamide

(535) The title compound was prepared in analogy to rac-4-(3-fluoro-2-hydroxypropoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 125) from 4-(2-((tert-butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(5-cyanopyridin-2-yl)piperazin-1-yl)phenyl)benzamide (93 mg, 157 μmol). Yield 67 mg (90%). Light yellow solid. LC-MS: m/z=476.4 [M+H].sup.+.

Example 130

rac-4-(3-Fluoro-2-hydroxypropoxy)-N-(4-(4-(thiazol-2-yl)piperazin-1-yl)phenyl)benzamide

(536) ##STR00221##

(537) The title compound was prepared in analogy to rac-4-(3-fluoro-2-hydroxypropoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 125) from rac-4-(2-((tert-butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(thiazol-2-yl)piperazin-1-yl)phenyl)benzamide (Example 126) (70.4 mg, 123 μmol). Yield 46 mg (82%). Light yellow solid. LC-MS: m/z=457.3 [M+H].sup.+.

Example 131

rac-N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-4-(3-fluoro-2-hydroxypropoxy)benzamide

(538) ##STR00222##

(539) The title compound was prepared in analogy to rac-4-(3-fluoro-2-hydroxypropoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 125) from rac-4-(2-((tert-butyldimethylsilyl)oxy)-3-fluoropropoxy)-N-(4-(4-(4-cyanophenyl)piperazin-1-yl)phenyl)benzamide (Example 127) (101 mg, 172 μmol). Yield 73 mg (90%). Light yellow solid. LC-MS: m/z=475.3 [M+H].sup.+.

Example 132

4-Methoxy-N-(4-((3aS,6aS)-5-(pyridin-2-yl)hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)phenyl)benzamide

(540) ##STR00223##

a) (3aR,6aR)-tert-Butyl 5-(pyridin-2-yl)hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate

(541) ##STR00224##

(542) To a solution of (3aR,6aR)-tert-butyl hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate hydrochloride (free base preparation: WO2014/139978 A1, WO2015/144605 A1) (995 mg, 4 mmol) in DMA (10 ml) was added at 22° C. 2-chloropyridine (1.36 g, 1.14 ml, 12 mmol) followed by Et.sub.3N (1.62 g, 2.23 ml, 16 mmol) and the mixture was set under Ar and reacted in a microwave apparatus at 160° C. for 30 min. The precipitated TEA.HCl was filtered off, washed with DMA (1×5 ml) and the filtrate was evaporated under high vacuum at 70° C. (Kugelrohr oven—0.8 mbar). The red oil was dissolved in DCM and directly purified by flash chromatography (silica gel, 40 g, EtOAc in heptane 20% to 40%) to give the title compound (261 mg, 23%) as an off-white solid. LC-MS: m/z=290.3 [M+H].sup.+.

b) (3aS,6aS)-2-(Pyridin-2-yl)octahydropyrrolo[3,4-c]pyrrole bis(2,2,2-trifluoroacetate)

(543) ##STR00225##

(544) To a solution of (3aR,6aR)-tert-butyl 5-(pyridin-2-yl)hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate (738 mg, 2.55 mmol) in DCM (7.2 ml) was added at 22° C. trifluoroacetic acid (5.82 g, 3.93 ml, 51 mmol). The reaction mixture was stirred at 22° C. for 30 min. The clear yellow solution was evaporated and the light brown oil was co-distilled with toluene (2 20×4 ml) to be solidified and dried under high vacuum at 55° C. to give the title compound (1.56 g, quant., ca. 68% purity) as off-white solid. LC-MS: m/z=190.2 [M+H].sup.+. This material was used in the next step with no further purification.

c) (3aS,6aS)-2-(4-Nitrophenyl)-5-(pyridin-2-yl)octahydropyrrolo[3,4-c]pyrrole

(545) ##STR00226##

(546) To a solution of (3aS,6aS)-2-(pyridin-2-yl)octahydropyrrolo[3,4-c]pyrrole bis (2,2,2-trifluoroacetate) (1.4 g, 2.28 mmol) in DMSO (5.6 ml) was added at 22° C. 1-fluoro-4-nitrobenzene (386 mg, 2.74 mmol) followed by K.sub.2CO.sub.3 (1.58 g, 11.4 mmol). The reaction mixture was heated to 90° C. and stirred at 90° C. for 30 min. The mixture was partitioned between H.sub.2O (100 ml) and DCM (100 ml) and the aqueous layer was extracted with DCM (3×100 ml). The combined organic layers were dried and evaporated. The crude product was suspended in DCM (10 ml), the solid filtered off, washed with DCM (2×5 ml) and dried to give the title compound (584 mg, 82%) as yellow solid. LC-MS: m/z=311.3 [M+H].sup.+.

d) 4-((3aS,6aS)-5-(Pyridin-2-yl)hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)aniline

(547) ##STR00227##

(548) To a suspension of (3aS,6aS)-2-(4-nitrophenyl)-5-(pyridin-2-yl)octahydropyrrolo[3,4-c]pyrrole (530 mg, 1.71 mmol) in EtOH (21 ml) was added at 22° C. after inertisation Pd/C 10% (90.9 mg, 85.4 μmol). The reaction mixture was set under H.sub.2 and stirred at 22° C. for 15 h. Acetic acid (21 ml) was added followed by new catalyst (90 mg). The mixture was stirred under H.sub.2 for 2 h. The catalyst was filtered off, washed with EtOH (2×20 ml), the filtrate was evaporated and co-distilled with EtOH (1×20 ml). The residue was treated with sat. aq. NaHCO.sub.3 (100 ml) and extracted with DCM (3×100 ml). The organic layers were dried and evaporated to give the title compound (405 mg, 85%) as light grey solid. MS: m/z=281.3 [M+H].sup.+.

e) 4-Methoxy-N-(4-((3aS,6aS)-5-(pyridin-2-yl)hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)phenyl)benzamide

(549) To a suspension of 4-((3aS,6aS)-5-(pyridin-2-yl)hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)aniline (56.1 mg, 200 μmol) in dioxane (2 ml) was added at 22° C. trimethylaluminum, 2 M in heptane (100 μl, 200 μmol) and the reaction mixture was stirred at 22° C. for 1 h. Then was added a solution of methyl 4-methoxybenzoate (33.2 mg, 200 μmol) in dioxane (0.4 ml), heated to 90° C. and stirred at 90° C. for 60 min. After a total 2 h at 90° C. the mixture was cooled to 22° C., quenched with H.sub.2O (1 ml), diluted with EtOAc (3 ml) and evaporated. The residue was treated with H.sub.2O (10 ml) and extracted with DCM (4×10 ml). The organic layer was dried (Na.sub.2SO.sub.4) and evaporated. The residue was purified by trituration in DCM (1 ml), the solid was filtered off, washed with DCM (2×2 ml) and dried in HV to give the title compound (7.8 mg, 9%) as a light yellow solid. The drying agent after extraction (Na.sub.2SO.sub.4) was suspended with 50 ml DCM/MeOH 19:1 containing 2% triethylamine, filtered and washed with DCM/MeOH 19:1. The filtrate was evaporated and dried in HV to give a second portion of the title compound (16.8 mg, 20%) as light yellow solid. Combined yield 25 mg (29%). LC-MS: m/z=415.4 [M+H].sup.+.

Example 133

4-Methoxy-N-(4-((3aR,6aR)-5-(pyridin-2-yl)hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)phenyl)benzamide

(550) ##STR00228##

a) (3aR,6aR)-tert-Butyl 5-(4-nitrophenyl)hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate

(551) ##STR00229##

(552) To a solution of (3aR,6aR)-tert-butyl hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate hydrochloride (free base preparation: WO2014/139978 A1, WO2015/144605 A1) (1.99 g, 8 mmol) in DMSO (8 ml) was added at 22° C. 1-fluoro-4-nitrobenzene (1.24 g, 8.8 mmol) followed by K.sub.2CO.sub.3 (2.76 g, 20 mmol). The reaction mixture was warmed to 90° C. and stirred at 90° C. for 90 min. The mixture was partitioned between H.sub.2O (100 ml) and DCM (100 ml) and the aqueous layer was extracted with DCM (3×100 ml). The organic layers were dried and evaporated. The residue was purified by flash chromatography (80 g silica gel, MeOH in DCM 0% to 2%) to give the title compound (1.9 g, 71%) as a yellow solid. LC-MS: m/z=334.2 [M+H].sup.+.

b) (3aS,6aS)-2-(4-Nitrophenyl)octahydropyrrolo[3,4-c]pyrrole 2,2,2-trifluoroacetate

(553) ##STR00230##

(554) To a solution of (3aR,6aR)-tert-butyl 5-(4-nitrophenyl)hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate (900 mg, 2.7 mmol) in DCM (9 ml) was added at 22° C. trifluoroacetic acid (6.16 g, 4.16 ml, 54 mmol) and the mixture was stirred at 22° C. for 60 min. The solvent was removed under reduced pressure to give the title compound (1.14 g, quant., ca. 82% purity) as yellow solid. LC-MS: m/z=234.2 [M+H].sup.+. This material was used in the next step with no further purification.

c) (3aR,6aR)-2-(4-Nitrophenyl)-5-(pyridin-2-yl)octahydropyrrolo[3,4-c]pyrrole

(555) ##STR00231##

(556) To a solution of (3aS,6aS)-2-(4-nitrophenyl)octahydropyrrolo[3,4-c]pyrrole 2,2,2-trifluoroacetate (550 mg, 1.58 mmol) in NMP (5.5 ml) was added at 22° C. 2-chloropyridine (899 mg, 749 μl, 7.92 mmol) followed by triethylamine (1.12 g, 1.55 ml, 11.1 mmol). The tube was inerted, sealed and reacted in microwave apparatus at 170° C. for 1.5 h. The mixture was quenched with sat aq. NaHCO.sub.3 (50 ml) and extracted DCM (4×50 ml). The organic layers were dried and evaporated (at the end HV at 100° C. to remove NMP). The crude product was suspended in DCM, the solid filtered off, washed with DCM and dried to give the title compound (265 mg, 54%) as brown solid. LC-MS: m/z=311.2 [M+H].sup.+.

d) 4-((3aR,6aR)-5-(Pyridin-2-yl)hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)aniline

(557) ##STR00232##

(558) The title compound was prepared in analogy to 4-((3aS,6aS)-5-(pyridin-2-yl)hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)aniline (Intermediate 132.d) from (3aR,6aR)-2-(4-nitrophenyl)-5-(pyridin-2-yl)octahydropyrrolo[3,4-c]pyrrole (468 mg, 1.51 mmol). 356 mg (84%). Light brown solid. MS: m/z=281.2 [M+H].sup.+.

e) 4-Methoxy-N-(4-((3aR,6aR)-5-(pyridin-2-yl)hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)phenyl)benzamide

(559) To a solution of 4-methoxybenzoic acid (29.2 mg, 192 μmol) in DMF (0.9 ml) was added at 22° C. HATU (73 mg, 192 μmol) followed by DIPEA (41.4 mg, 55.9 μl, 320 μmol) and the mixture was stirred at 22° C. for 30 min. Then was added 4-((3aR,6aR)-5-(pyridin-2-yl)hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)aniline (44.9 mg, 160 μmol) to give after 5 minutes a thick suspension that was diluted by addition of DMF (0.45 ml). After stirring at 22° C. for further 3 h the mixture was quenched with H.sub.2O (10 ml) and extracted with DCM (5×10 ml). The organic layers were dried and evaporated and the crude product was suspended in 5 ml DCM for 1 h. The solid was filtered off, washed with DCM (2×1 ml) and dried under high vacuum to give the title compound (58 mg, 88%) as light grey solid. LC-MS: m/z=415.3 [M+H].sup.+.

Example 134

4-(Fluoromethoxy)-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide

(560) ##STR00233##

a) 4-(Fluoromethoxy)benzoic acid

(561) ##STR00234##

(562) To a solution of methyl 4-(fluoromethoxy)benzoate (360 mg, 1.95 mmol) in THF (5 ml) and EtOH (5 ml) was added NaOH 1 M in H.sub.2O (3.91 ml, 3.91 mmol) and the clear and colorless solution was stirred at rt for 5 h. The organic solvents were removed by evaporation and the aqueous residue was treated dropwise with HCl 1 M in H.sub.2O (3.91 ml, 3.91 mmol). The resulting white suspension was filtered, washed with H.sub.2O and dried. Colorless solid (280 mg, 84%). LC-MS: m/z=169.1 [M−H].sup.−.

b) 4-(Fluoromethoxy)-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide

(563) To a solution of 4-(fluoromethoxy)benzoic acid (93.6 mg, 0.55 mmol) in DCM (8 ml) was added at 22° C. oxalyl chloride (105 mg, 72.2 μl, 825 μmol) followed by DMF (8.04 mg, 8.52 μl, 110 μmol) and the mixture was stirred at 22° C. for 90 min. The solvent and excess of oxalyl chloride were removed under reduced pressure to give the crude acid chloride that was used without further purification. To a solution of 4-(4-(pyridin-3-yl)piperazin-1-yl)aniline (Intermediate 37.b) (140 mg, 0.55 mmol) in DCM (6 ml) was added at 22° C. DIPEA (284 mg, 384 μl, 2.2 mmol) followed by a solution of the acid chloride in DCM (2 ml) and the mixture was stirred at 22° C. for 15 h. The thick suspension was evaporated, suspended in DCM/MeOH 3:1 (4 ml) and the solid was filtered off, washed with DCM/MeOH 3:1 (1×3 ml) and dried under high vacuum to give the title compound (150 mg, 67%) as off-white solid. LC-MS: m/z=407.3 [M+H)].sup.+.

Example 135

4-(Fluoromethoxy)-N-[4-(4-pyridin-2-ylpiperazin-1-yl)phenyl]benzamide

(564) ##STR00235##

(565) The title compound was prepared in analogy to 4-(fluoromethoxy)-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide (Example 134, step b) from 4-(fluoromethoxy)benzoic acid (Intermediate 134 a) (55 mg, 323 μmol) and 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (82.2 mg, 323 μmol). Yield 91 mg (69%). Off-white solid. LC-MS: m/z=407.3 [M+H)].sup.+.

Example 136

N-[4-[4-(5-Cyanopyridin-2-yl)piperazin-1-yl]phenyl]-4-(fluoromethoxy)benzamide

(566) ##STR00236##

(567) The title compound was prepared in analogy to 4-(fluoromethoxy)-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide (Example 134, step b) from 4-(fluoromethoxy)benzoic acid (Intermediate 134 a) (55 mg, 323 μmol) and 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-3-carbonitrile (Intermediate 50.a) (90.3 mg, 323 μmol). Yield 69 mg (49%). Off-white solid. LC-MS: m/z=430.4 [M−H].sup.−.

Example 137

4-(2-(2-Hydroxyethoxy)ethoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(568) ##STR00237##

a) 4-((4-(4-(Pyridin-2-yl)piperazin-1-yl)phenyl)carbamoyl)phenyl acetate

(569) ##STR00238##

(570) 4-Acetoxybenzoic acid (1.5 g, 8.33 mmol) was dissolved in DCM (60 ml). Oxalyl chloride (1.58 g, 1.09 ml, 12.5 mmol) was added followed by DMF (30.4 mg, 32.2 μl, 416 μmol). The reaction mixture was stirred for 1.5 h at rt, then concentrated under vacuum. The crude product was dissolved in DCM (35 ml) and added dropwise to a stirred solution of 4-(4-(pyridin-2-yl)piperazin-1-yl)aniline (Intermediate 1.b) (2.12 g, 8.33 mmol) and DIPEA (4.31 g, 5.82 ml, 33.3 mmol) in DCM (70 ml) at RT. The reaction mixture was stirred at rt for 1.25 h. To the light brown suspension was added a mixture of MeOH (6 ml) and H.sub.2O (30 ml) and the reaction mixture was allowed to stir for 15 minutes before filtering off the product. The filter cake was washed with DCM (20 ml) and H.sub.2O (2×30 ml). Colorless solid (2.89 g, 83%), LCMS: m/z=417.3 [M+H].sup.+.

b) 4-Hydroxy-N-[4-(4-pyridin-2-ylpiperazin-1-yl)phenyl]benzamide

(571) ##STR00239##

(572) To a suspension of 4-((4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)carbamoyl)phenyl acetate (1.68 g, 4.03 mmol) in dioxane (34 ml) and H.sub.2O (16.8 ml) was added NaOH 1M in H.sub.2O (16.1 ml, 16.1 mmol) and the rapidly formed solution was stirred at 60° C. for 1.3 h. Dioxane was evaporated and to the residue was added dropwise HCl 1 M in H.sub.2O (14.5 ml, 14.5 mmol). The mixture was filtered. The filter cake was washed with plenty of H.sub.2O and dried. Light grey solid (1.49 g; 99%). LC-MS: m/z=373.3 [M−H].sup.−.

c) 4-(2-(2-Hydroxyethoxy)ethoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(573) To a suspension of 4-hydroxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (112 mg, 0.3 mmol) in DMF (2.2 ml) was added at 22° C. 2-(2-hydroxyethoxy)ethyl 4-methylbenzenesulfonate (CAS Nr. 118591-58-5) (85.9 mg, 330 μmol) followed by Cs.sub.2CO.sub.3 (108 mg, 330 μmol) and the mixture was stirred at 22° C. for 1 h. Then the mixture was warmed to 70° C. and stirred for 2 h. The mixture was cooled to 22° C. and treated dropwise with H.sub.2O (2.2 ml) to give precipitation of a solid. The suspension was stirred for 10 minutes, the solid was filtered off, washed with MeOH/H.sub.2O 1:1 (2×6 ml) and H.sub.2O (2×6 ml) and dried. The resulting solid was dissolved in DCM/MeOH 1:1 (10 ml), filtered and the filter washed with DCM/MeOH 1:1 (1×2 ml). The filtrate was evaporated and dried under high vacuum to give the title compound (60 mg, 43%) as white solid. LC-MS: m/z=463.3 [M+H].sup.+.

Example 138

4-Hydroxy-N-[4-(4-pyridin-3-ylpiperazin-1-yl)phenyl]benzamide

(574) ##STR00240##

a) [4-[[4-(4-Pyridin-3-ylpiperazin-1-yl)phenyl]carbamoyl]phenyl] acetate

(575) ##STR00241##

(576) The title compound was prepared in analogy to 4-((4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)carbamoyl)phenyl acetate (Intermediate 137.a) from 4-acetoxybenzoic acid (819 mg, 4.55 mmol) and 4-(4-(pyridin-3-yl)piperazin-1-yl)aniline (Intermediate 37.b) (1.10 g, 4.33 mmol). Yield 1.39 g (77%). LC-MS: m/z=417.2[M+H].sup.+.

b) 4-Hydroxy-N-[4-(4-pyridin-3-ylpiperazin-1-yl)phenyl]benzamide

(577) To a suspension of [4-[[4-(4-pyridin-3-ylpiperazin-1-yl)phenyl]carbamoyl]phenyl] acetate (1.39 g, 3.33 mmol) in MeOH (41.5 ml) was added 1 M aq. NaOH (13.3 ml, 13.3 mmol) and the resulting mixture was stirred for 20 min at rt. The reaction mixture was treated with 1 M HCl aq. (13.3 ml, 13.3 mmol) to give precipitation of the product. After stirring for 1 h at rt the solids were collected by filtration and washed with H.sub.2O/MeOH 1:1 (30 ml) and H.sub.2O (2×30 ml) and dried under high vacuum over night to obtain the product (1.01 g, 81%) as off-white solid. LC-MS: m/z=373.1 [M−H].sup.−.

General Synthesis Sub-Series

(578) ##STR00242##

N-(4-Bromophenyl)-4-methoxybenzamide

(579) ##STR00243##

(580) To a solution of 4-bromoaniline (5 g, 29.1 mmol) and DIPEA (14.2 ml, 81.4 mmol) in DCM (50 ml) at 0° C. was added dropwise a solution of 4-methoxybenzoyl chloride (5 g, 29.3 mmol) in DCM (50 ml). The reaction mixture was stirred at 0° C. for 30 minutes and then at rt for 1 h. The precipitate formed was collected by filtration, washed with DCM and dried to give the title compound (7.56 g, 85%) as a white solid.

(581) .sup.1H NMR (400 MHz, DMSO): δ 10.21 (s, 1H), 7.98-7.95 (m, 2H), 7.78-7.75 (m, 2H), 7.55-7.52 (m, 2H), 7.08 (d, J=8.9 Hz, 2H), 3.85 (s, 3H). LC-MS: Rt=1.64 min m/z=306, [M+H].sup.+.

Benzyl 4-(4-(4-methoxybenzamido)phenyl)piperazine-1-carboxylate

(582) ##STR00244##

(583) N-(4-Bromophenyl)-4-methoxybenzamide (2 g, 6.53 mmol), Cbz-piperazine (1.38 g, 7.18 mmol), XPhos (623 mg, 1.31 mmol) and NaOtBu (1.38 g, 14.4 mmol) were suspended in dioxane (20 ml) and degassed with nitrogen for 30 minutes. [Pd.sub.2(dba).sub.3] (598 mg, 0.65 mmol) was then added and the reaction mixture was heated to 90° C. for 2 h under N.sub.2. The reaction was allowed to cool to rt and diluted with H.sub.2O. The precipitate formed was collected by filtration and washed with H.sub.2O. The dry residue (3.7 g) was triturated with diethyl ether to afford the title compound (2.85 g, 98%) as a brown solid.

(584) .sup.1H NMR (400 MHz, DMSO): δ 9.92 (s, 1H), 7.94 (d, J=8.9 Hz, 2H), 7.62 (d, J=9.2 Hz, 2H), 7.40 (d, J=4.5 Hz, 4H), 7.38-7.31 (m, 1H), 7.05 (d, J=8.9 Hz, 2H), 6.95 (d, J=9.2 Hz, 2H), 5.12 (s, 2H), 3.84 (s, 3H), 3.59-3.56 (m, 4H), 3.09 (dd, J=5.0, 5.0 Hz, 4H). LC-MS: Rt=1.69 min, m/z=446, [M+H].sup.+.

4-Methoxy-N-(4-(piperazin-1-yl)phenyl)benzamide

(585) ##STR00245##

(586) To a solution of benzyl 4-(4-(4-methoxybenzamido)phenyl)piperazine-1-carboxylate (2 g, 4.49 mmol) in EtOH (36 ml) was added Pd/C 10% (2 g), followed by 1-methyl-1,4-cyclohexadiene (5 ml, 44.9 mmol). The reaction mixture was heated to 85° C. and stirred at this temperature for 1 hour. After cooling to rt, the reaction mixture was filtered through a pad of Celite and washed with EtOH and MeOH. The filtrate was concentrated to furnish the title compound (1.33 g, 95%) as a brown solid.

(587) .sup.1H NMR (400 MHz, DMSO): δ d 9.88 (s, 1H), 7.94 (d, J=8.9 Hz, 2H), 7.59 (d, J=9.0 Hz, 2H), 7.05 (d, J=8.9 Hz, 2H), 6.90 (d, J=9.2 Hz, 2H), 3.84 (s, 3H), 3.02-2.98 (m, 4H), 2.83 (dd, J=4.9, 4.9 Hz, 4H). LC-MS: Rt=1.17 min, m/z=312, [M+H].sup.+.

General Procedure A

Synthesis of 4-methoxy-N-(4-(4-(R.SUB.2.-yl)piperazin-1-yl)phenyl)benzamides

(588) ##STR00246##

(589) 4-Methoxy-N-(4-(piperazin-1-yl)phenyl)benzamide (120 mg, 0.39 mmol), the R.sub.2-(Het)aryl halide (1.1 eq.), Cs.sub.2CO.sub.3 (2.2 eq., 276 mg, 0.85 mmol), [Pd(OAc).sub.2] (0.1 eq., 9 mg, 0.04 mmol) and RuPhos (0.2 eq., 36 mg, 0.08 mmol) were combined in a reaction tube. Degassed dioxane (3 ml) was then added, the reaction tube flushed with nitrogen, sealed and the reaction mixture was stirred at 80° C. overnight. In case of incomplete conversions more reagents were added accordingly. After completion the reaction mixture was cooled to rt and H.sub.2O added. The precipitate formed was collected by filtration, washed with H.sub.2O and dried. The residue was dissolved in DCM/MeOH (2:1), adsorbed onto HM-N beads (Biotage) and evaporated. The resulting material was dry-loaded onto a silica column and purified by flash column chromatography eluting with 0.5 to 3% methanol/dichloromethane to afford the title compounds as yellow solids.

Examples Prepared Using General Procedure A

Example 139

N-(4-(4-(4-Cyano-2-methoxyphenyl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(590) ##STR00247##

(591) Yield: 47 mg.

(592) .sup.1H NMR (400 MHz, DMSO): δ 9.92 (s, 1H), 7.95 (d, J=8.8 Hz, 2H), 7.63 (d, J=9.2 Hz, 2H), 7.38 (s, 2H), 7.07-7.03 (m, 3H), 6.99 (d, J=9.2 Hz, 2H), 3.88 (s, 3H), 3.85 (s, 3H), 3.25 (s, 4H) 4H-piperazine hidden under DMSO peak.

(593) LC-MS: Rt=3.36 min, m/z=443 [M+H].sup.+.

Example 140

N-(4-(4-(4-Cyano-3-methoxyphenyl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(594) ##STR00248##

(595) Yield: 33 mg.

(596) .sup.1H NMR (400 MHz, DMSO): δ 9.92 (s, 1H), 7.95 (d, J=8.9 Hz, 2H), 7.64 (d, J=9.2 Hz, 2H), 7.47 (d, J=8.5 Hz, 1H), 7.06 (d, J=9.0 Hz, 2H), 7.00 (d, J=9.2 Hz, 2H), 6.68-6.64 (m, 2H), 3.91 (s, 3H), 3.84 (s, 3H), 3.54 (dd, J=5.1, 5.1 Hz, 4H), 3.25 (dd, J=5.1, 5.1 Hz, 4H).

(597) LC-MS: Rt=3.33 min, m/z=443 [M+H].sup.+.

Example 141

N-(4-(4-(5-Fluoropyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(598) ##STR00249##

(599) Yield: 5 mg.

(600) .sup.1H NMR (400 MHz, DMSO): δ 9.95 (s, 1H), 8.17 (d, J=3.3 Hz, 1H), 8.00-7.97 (m, 2H), 7.67 (d, J=9.1 Hz, 2H), 7.62-7.55 (m, 1H), 7.09 (d, J=8.8 Hz, 2H), 7.05-6.98 (m, 3H), 3.88 (s, 3H), 3.63 (dd, J=5.1, 5.1 Hz, 4H), 3.25 (dd, J=5.2, 5.2 Hz, 4H).

(601) LC-MS: Rt=3.33 min, m/z=407 [M+H].sup.+.

Example 142

N-(4-(4-(5-(Dimethylamino)pyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(602) ##STR00250##

(603) Yield: 28 mg.

(604) .sup.1H NMR (400 MHz, DMSO): δ 9.91 (s, 1H), 7.95 (d, J=8.9 Hz, 2H), 7.78 (d, J=3.0 Hz, 1H), 7.63 (d, J=9.2 Hz, 2H), 7.20 (dd, J=3.1, 9.2 Hz, 1H), 7.05 (d, J=8.9 Hz, 2H), 6.99 (d, J=9.2 Hz, 2H), 6.85 (d, J=9.0 Hz, 1H), 3.84 (s, 3H), 3.46 (dd, J=5.0, 5.0 Hz, 4H), 3.21 (dd, J=5.1, 5.1 Hz, 4H), 2.80 (s, 6H).

(605) LC-MS: Rt=2.87 min, m/z=432 [M+H].sup.+.

Example 143

N-(4-(4-(5-Cyanopyrimidin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(606) ##STR00251##

(607) Yield: 76 mg.

(608) .sup.1H NMR (400 MHz, DMSO): δ 9.92 (s, 1H), 8.80 (s, 2H), 7.95 (d, J=9.0 Hz, 2H), 7.64 (d, J=9.2 Hz, 2H), 7.05 (d, J=9.0 Hz, 2H), 6.99 (d, J=9.2 Hz, 2H), 4.01 (dd, J=5.2, 5.2 Hz, 4H), 3.84 (s, 3H), 3.21 (dd, J=5.1, 5.1 Hz, 4H).

(609) LC-MS: Rt=3.41 min, m/z=415, [M+H].sup.+.

Example 144

N-(4-(4-(4-Cyano-2-methylphenyl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(610) ##STR00252##

(611) Yield: 32 mg.

(612) .sup.1H NMR (400 MHz, DMSO): δ 9.92 (s, 1H), 7.95 (d, J=8.9 Hz, 2H), 7.66-7.62 (m, 4H), 7.20-7.16 (m, 1H), 7.06 (d, J=9.0 Hz, 2H), 7.00 (d, J=9.2 Hz, 2H), 3.84 (s, 3H), 3.31-3.25 (m, 4H), 3.11 (dd, J=4.8, 4.8 Hz, 4H), 2.33 (s, 3H).

(613) LC-MS: Rt=3.49 min, m/z=427 [M+H].sup.+.

Example 145

N-(4-(4-(4-Cyano-2-fluorophenyl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(614) ##STR00253##

(615) Yield: 39 mg.

(616) .sup.1H NMR (400 MHz, DMSO): δ 9.92 (s, 1H), 7.95 (d, J=8.9 Hz, 2H), 7.74 (dd, J=2.0, 13.3 Hz, 1H), 7.66-7.59 (m, 3H), 7.21 (dd, J=8.8, 8.8 Hz, 1H), 7.06 (d, J=8.9 Hz, 2H), 7.00 (d, J=9.2 Hz, 2H), 3.84 (s, 3H), 3.39-3.34 (m, 4H), 3.31-3.24 (m, 4H).

(617) LC-MS: Rt=3.41 min, m/z=431 [M+H].sup.+.

Example 146

N-(4-(4-(6-Fluoropyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(618) ##STR00254##

(619) Yield: 10 mg.

(620) .sup.1H NMR (400 MHz, DMSO): δ 9.96 (s, 1H), 7.99 (d, J=8.8 Hz, 2H), 7.76 (q, J=8.3 Hz, 1H), 7.68 (d, J=8.8 Hz, 2H), 7.10 (d, J=8.6 Hz, 2H), 7.04 (d, J=8.8 Hz, 2H), 6.80 (d, J=8.1 Hz, 1H), 6.38-6.34 (m, 1H), 3.89 (s, 3H), 3.68 (s, 4H), 3.25 (d, J=4.3 Hz, 4H).

(621) LC-MS: Rt=3.48 min, m/z=407 [M+H].sup.+.

Example 147

N-(4-(4-(5-Cyanopyrazin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(622) ##STR00255##

(623) Yield: 39 mg.

(624) .sup.1H NMR (400 MHz, DMSO): δ 9.96 (s, 1H), 8.64 (d, J=1.3 Hz, 1H), 8.55 (d, J=1.3 Hz, 1H), 7.99 (d, J=8.8 Hz, 2H), 7.68 (d, J=9.1 Hz, 2H), 7.09 (d, J=8.8 Hz, 2H), 7.04 (d, J=9.1 Hz, 2H), 3.95 (dd, J=5.2, 5.2 Hz, 4H), 3.89 (s, 3H), 3.35-3.25 (m, 4H).

(625) LC-MS: Rt=3.21 min, m/z=415 [M+H].sup.+.

Example 148

N-(4-(4-(3-Fluoropyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(626) ##STR00256##

(627) Yield: 41 mg.

(628) .sup.1H NMR (400 MHz, DMSO): δ 9.83 (s, 1H), 7.99-7.95 (m, 1H), 7.87 (d, J=8.8 Hz, 2H), 7.56 (d, J=9.1 Hz, 2H), 7.51-7.44 (m, 1H), 6.97 (d, J=8.8 Hz, 2H), 6.91 (d, J=9.1 Hz, 2H), 6.88-6.82 (m, 1H), 3.77 (s, 3H), 3.51-3.44 (m, 4H), 3.17 (dd, J=5.1, 5.1 Hz, 4H).

(629) LC-MS: Rt=3.37 min, m/z=407 [M+H].sup.+.

Example 149

N-(4-(4-(4-Chloropyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(630) ##STR00257##

(631) Yield: 6 mg.

(632) .sup.1H NMR (400 MHz, DMSO): δ 9.96 (s, 1H), 8.15 (d, J=5.6 Hz, 1H), 7.99 (d, J=8.8 Hz, 2H), 7.68 (d, J=8.8 Hz, 2H), 7.10 (d, J=8.8 Hz, 2H), 7.04 (d, J=9.3 Hz, 3H), 6.79 (dd, J=1.5, 5.3 Hz, 1H), 3.89 (s, 3H), 3.73 (dd, J=4.9, 4.9 Hz, 4H), 3.24 (dd, J=4.9, 4.9 Hz, 4H).

(633) LC-MS: Rt=3.39 min, m/z=423 [M+H].sup.+.

Example 150

N-(4-(4-(4-Cyano-3-fluorophenyl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(634) ##STR00258##

(635) Yield: 35 mg.

(636) .sup.1H NMR (400 MHz, DMSO): δ 9.96 (s, 1H), 7.99 (d, J=8.8 Hz, 2H), 7.70-7.64 (m, 3H), 7.12-6.95 (m, 6H), 3.89 (s, 3H), 3.61 (dd, J=5.1, 5.1 Hz, 4H), 3.27 (dd, J=4.9, 4.9 Hz, 4H).

(637) LC-MS: Rt=3.39 min, m/z=431 [M+H].sup.+.

Example 151

N-(4-(4-(5-Cyano-4-methylpyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(638) ##STR00259##

(639) Yield: 38 mg.

(640) .sup.1H NMR (400 MHz, DMSO): δ 9.96 (s, 1H), 8.48 (s, 1H), 8.00 (d, J=8.8 Hz, 2H), 7.68 (d, J=9.1 Hz, 2H), 7.10 (d, J=8.8 Hz, 2H), 7.06-6.99 (m, 3H), 3.89 (s, 3H), 3.86 (dd, J=5.2, 5.2 Hz, 4H), 3.25 (dd, J=5.2, 5.2 Hz, 4H), 2.41 (s, 3H).

(641) LC-MS: Rt=3.38 min, m/z=428 [M+H].sup.+.

Example 152

N-(4-(4-(4-Chloro-5-cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(642) ##STR00260##

(643) Yield: 7 mg.

(644) .sup.1H NMR (400 MHz, DMSO): δ 9.84 (s, 1H), 8.50 (s, 1H), 7.87 (d, J=8.8 Hz, 2H), 7.56 (d, J=9.1 Hz, 2H), 7.20 (s, 1H), 6.98 (d, J=8.8 Hz, 2H), 6.92 (d, J=9.1 Hz, 2H), 3.81 (dd, J=4.9, 4.9 Hz, 4H), 3.14 (dd, J=5.1, 5.1 Hz, 4H).

(645) LC-MS: Rt=3.48 min, m/z=448 [M+H].sup.+.

Example 153

N-(4-(4-(4-Cyano-3-methylphenyl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(646) ##STR00261##

(647) Yield: 51 mg.

(648) .sup.1H NMR (400 MHz, DMSO): δ 9.92 (s, 1H), 7.95 (d, J=8.9 Hz, 2H), 7.64 (d, J=9.0 Hz, 2H), 7.54 (d, J=8.8 Hz, 1H), 7.07-6.98 (m, 5H), 6.93 (dd, J=2.5, 8.8 Hz, 1H), 3.84 (s, 3H), 3.50 (dd, J=5.1, 5.1 Hz, 4H), 3.24 (dd, J=5.1, 5.1 Hz, 4H), 2.41 (s, 3H).

(649) LC-MS: Rt=3.41 min, m/z=427 [M+H].sup.+.

Example 154

N-(4-(4-(6-Cyanopyridin-3-yl)piperazin-1-yl)phenyl)-4-methoxybenzamide

(650) ##STR00262##

(651) Yield: 15 mg.

(652) .sup.1H NMR (400 MHz, DMSO): δ 9.99 (s, 1H), 8.57 (d, J=2.5 Hz, 1H), 8.01 (d, J=8.6 Hz, 2H), 7.85 (d, J=8.8 Hz, 1H), 7.71 (d, J=9.1 Hz, 2H), 7.52 (dd, J=2.8, 8.8 Hz, 1H), 7.12 (d, J=8.6 Hz, 2H), 7.07 (d, J=8.8 Hz, 2H), 3.91 (s, 3H), 3.65 (dd, J=5.1, 5.1 Hz, 4H), 3.34-3.32 (m, 4H).

(653) LC-MS: Rt=3.64 min, m/z=414 [M+H].sup.+.

Example 155

4-Methoxy-N-(4-(4-(2-methoxypyridin-4-yl)piperazin-1-yl)phenyl)benzamide

(654) ##STR00263##

(655) Yield: 44 mg.

(656) .sup.1H NMR (400 MHz, DMSO): δ 9.93 (s, 1H), 7.95 (d, J=8.9 Hz, 2H), 7.83 (d, J=6.0 Hz, 1H), 7.64 (d, J=9.0 Hz, 2H), 7.05 (d, J=8.9 Hz, 2H), 6.98 (d, J=9.2 Hz, 2H), 6.64 (dd, J=2.3, 6.1 Hz, 1H), 6.19 (d, J=2.1 Hz, 1H), 3.81 (d, J=21.0 Hz, 6H), 3.44 (dd, J=5.1, 5.1 Hz, 4H), 3.23-3.17 (m, 4H).

(657) LC-MS: Rt=3.15 min, m/z=419 [M+H].sup.+.

Example 156

4-Methoxy-N-(4-(4-(6-methylpyridin-3-yl)piperazin-1-yl)phenyl)benzamide

(658) ##STR00264##

(659) Yield: 43 mg.

(660) .sup.1H NMR (400 MHz, DMSO): δ 9.93 (s, 1H), 8.22 (d, J=2.8 Hz, 1H), 7.95 (d, J=8.9 Hz, 2H), 7.64 (d, J=8.9 Hz, 2H), 7.33 (dd, J=2.9, 8.5 Hz, 1H), 7.11 (d, J=8.5 Hz, 1H), 7.05 (d, J=8.8 Hz, 2H), 7.00 (d, J=9.0 Hz, 2H), 3.84 (s, 3H), 3.27 (d, J=4.5 Hz, 8H), 2.37 (s, 3H).

(661) LC-MS: Rt=2.50 min, m/z=403 [M+H].sup.+.

General Synthesis Sub-Series 2

(662) ##STR00265##

6-(4-(4-Nitrophenyl)piperazin-1-yl)nicotinonitrile

(663) ##STR00266##

(664) 1-(4-Nitrophenyl)piperazine (1.5 g, 7.24 mmol), 6-bromopyridine-3-carbonitrile (1.46 g, 7.96 mmol), Cs.sub.2CO.sub.3 (5.19 g, 15.9 mmol) and RuPhos (675 mg, 1.45 mmol) were suspended in anhydrous dioxane (50 ml) and degassed for 5 minutes with nitrogen. [Pd(OAc).sub.2](162 mg, 0.72 mmol) was then added, the mixture further degassed (3 min) and the reaction vessel was sealed and heated at 90° C. overnight. After cooling to rt H.sub.2O was added and the resulting precipitate collected by filtration. The precipitate was washed with H.sub.2O (3×) and diethyl ether (3×) and dried to give the title compound (1.75 g, 80%) as a dark yellow solid.

(665) .sup.1H NMR (400 MHz, DMSO): δ 8.58 (d, J=1.5 Hz, 1H), 8.14 (d, J=9.3 Hz, 2H), 7.95 (dd, J=2.3, 9.1 Hz, 1H), 7.08 (d, J=9.6 Hz, 2H), 7.00 (d, J=9.3 Hz, 1H), 3.94-3.87 (m, 4H), 3.71 (dd, J=5.1, 5.1 Hz, 4H). LC-MS: Rt=1.60 min, m/z=310 [M+H].sup.+.

4-(4-(4-Nitrophenyl)piperazin-1-yl)benzonitrile

(666) ##STR00267##

(667) 1-(4-Nitrophenyl)piperazine (1.5 g, 7.24 mmol), 4-bromobenzonitrile (1.45 g, 7.96 mmol), Cs.sub.2CO.sub.3 (5.19 g, 15.9 mmol) and RuPhos (675 mg, 1.45 mmol) were suspended in anhydrous dioxane (50 ml) and degassed for 5 min with nitrogen. [Pd(OAc).sub.2] (162 mg, 0.72 mmol) was then added, the mixture further degassed (3 min) and the reaction vessel was sealed and heated at 90° C. overnight. After cooling to rt H.sub.2O was added and the resulting precipitate collected by filtration. The precipitate was washed with H.sub.2O (3×) and diethyl ether (3×) and dried to give the title compound (1.70 g, 77%) as a dark yellow solid.

(668) .sup.1H NMR (400 MHz, DMSO): δ 8.14 (d, J=9.1 Hz, 2H), 7.67 (d, J=8.6 Hz, 2H), 7.12-7.05 (m, 4H), 3.72 (m, 4H), 3.62 (m, 4H). LC-MS: Rt=1.65 min, m/z=307 [M−H].sup.−.

6-[4-(4-Aminophenyl)piperazin-1-yl]pyridine-3-carbonitrile (corresponds to Intermediate 50.a)

(669) ##STR00268##

(670) 6-(4-(4-Nitrophenyl)piperazin-1-yl)nicotinonitrile (2.2 g, 7.11 mmol) was suspended in EtOH (71 ml) and H.sub.2O (18 ml), NH.sub.4Cl (228 mg, 4.27 mmol) was added and the mixture heated at 40° C. Iron powder (2.39 g, 42.7 mmol) was then added and the mixture was stirred at 90° C. for 2 h. After cooling to rt the reaction mixture was filtered and partitioned between DCM and saturated NaHCO.sub.3. The aqueous phase was extracted with DCM (3×) and the combined organic phases dried (Na.sub.2SO.sub.4), filtered and evaporated. The residue was re-dissolved in chloroform and evaporated (3×) to provide the title compound (2.2 g, quant.) as a dark solid.

(671) .sup.1H NMR (400 MHz, DMSO): δ 8.55 (d, J=2.0 Hz, 1H), 7.91 (dd, J=2.4, 9.0 Hz, 1H), 7.03 (d, J=9.3 Hz, 1H), 6.80 (d, J=8.8 Hz, 2H), 6.56 (d, J=8.6 Hz, 2H), 4.70-4.64 (m, 2H), 3.82 (dd, J=4.9, 4.9 Hz, 4H), 3.03 (dd, J=4.9, 4.9 Hz, 4H). LC-MS: Rt=1.24 min, m/z=280 [M+H].sup.+.

4-(4-(4-Aminophenyl)piperazin-1-yl)benzonitrile (corresponds to Intermediate 57.a)

(672) ##STR00269##

(673) 4-(4-(4-Nitrophenyl)piperazin-1-yl)benzonitrile (2.2 g, 7.14 mmol) was suspended in EtOH (71 ml) and H.sub.2O (18 ml), NH.sub.4Cl (228 mg, 4.27 mmol) was added and the mixture heated at 40° C. Iron powder (2.39 g, 42.7 mmol) was then added and the mixture was stirred at 90° C. for 2 h. After cooling to rt the reaction mixture was filtered and partitioned between DCM and saturated NaHCO.sub.3. The aqueous phase was extracted with DCM (3×) and the combined organic phases dried (Na.sub.2SO.sub.4), filtered and evaporated. The residue was re-dissolved in chloroform and evaporated (3×) to provide the title compound (1.98 g, 99%) as a dark solid.

(674) .sup.1H NMR (400 MHz, DMSO): δ 7.62 (d, J=8.8 Hz, 2H), 7.09 (d, J=9.1 Hz, 2H), 6.76 (d, J=8.6 Hz, 2H), 6.54 (d, J=8.6 Hz, 2H), 4.63 (s, 2H), 3.47 (dd, J=4.7, 4.7 Hz, 4H), 3.04 (dd, J=4.7, 4.7 Hz, 4H). LC-MS: Rt=1.34 min, m/z=279 [M+H].sup.+.

General Procedure B

Synthesis of N-(4-(4-(5-cyanopyridin-2-yl)piperazin-1-yl)phenyl)-R.SUB.1.-amides and N-(4-(4-(4-cyanophenyl)piperazin-1-yl)phenyl)-R.SUB.1.-amides

(675) ##STR00270##

(676) To a solution of the R.sub.1-carboxylic acids (1.1 eq.) in anhydrous DMF (2 ml) and DIPEA (1.5 eq., 103 μL, 0.59 mmol) was added HATU (1.2 eq., 180 mg, 0.47 mmol) and the reaction mixture stirred for 30 minutes at rt. The amines 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-3-carbonitrile (110 mg, 0.39 mmol) or 4-(4-(4-aminophenyl)piperazin-1-yl)benzonitrile (110 mg, 0.4 mmol) were then added in DMF (2 ml) and the reaction was stirred at rt overnight. H.sub.2O was then added and the resulting precipitate collected by filtration. The precipitate was washed with H.sub.2O and dried. The crude solid was dissolved in DCM/MeOH (2:1), adsorbed onto HM-N beads (Biotage) and evaporated. The resulting material was dry-loaded onto a silica column and purified by flash column chromatography eluting with 0.5 to 3% MeOH/DCM to afford the title compounds as yellow solids.

Examples Prepared Using General Procedure B

Example 157

N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-6-methoxynicotinamide

(677) ##STR00271##

(678) Yield: 19 mg.

(679) .sup.1H NMR (400 MHz, DMSO): δ 10.08 (s, 1H), 8.78 (d, J=2.1 Hz, 1H), 8.23 (dd, J=2.5, 8.7 Hz, 1H), 7.63 (dd, J=2.4, 9.1 Hz, 4H), 7.11 (d, J=9.2 Hz, 2H), 7.02 (d, J=9.2 Hz, 2H), 6.96 (d, J=8.7 Hz, 1H), 3.95 (s, 3H), 3.52 (dd, J=5.1, 5.1 Hz, 4H), 3.26 (dd, J=5.1, 5.1 Hz, 4H). LC-MS: Rt=3.33 min, m/z=414 [M+H].sup.+.

Example 158

N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-1-methyl-1H-pyrazole-4-carboxamide

(680) ##STR00272##

(681) Yield: 24 mg.

(682) .sup.1H NMR (400 MHz, DMSO): δ 9.65 (s, 1H), 8.27 (s, 1H), 7.99 (s, 1H), 7.60 (dd, J=9.0, 17.9 Hz, 4H), 7.11 (d, J=9.0 Hz, 2H), 6.99 (d, J=9.0 Hz, 2H), 3.90 (s, 3H), 3.51 (dd, J=5.1, 5.1 Hz, 4H), 3.24 (dd, J=5.1, 5.1 Hz, 4H). LC-MS: Rt=3.16 min, m/z=387 [M+H].sup.+.

Example 159

N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-3,4-dimethoxybenzamide

(683) ##STR00273##

(684) Yield: 62 mg.

(685) .sup.1H NMR (400 MHz, DMSO): δ 9.94 (s, 1H), 8.57 (d, J=2.3 Hz, 1H), 7.93 (dd, J=2.3, 9.1 Hz, 1H), 7.69-7.62 (m, 3H), 7.58 (d, J=1.8 Hz, 1H), 7.12 (d, J=8.3 Hz, 1H), 7.05 (dd, J=8.7, 8.7 Hz, 3H), 3.90-3.83 (m, 10H), 3.30-3.22 (m, 4H). LC-MS: Rt=3.23 min, m/z=444 [M+H].sup.+.

Example 160

N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-3-fluoro-4-methoxybenzamide

(686) ##STR00274##

(687) Yield: 66 mg.

(688) .sup.1H NMR (400 MHz, DMSO): δ 10.02 (s, 1H), 8.57 (d, J=2.3 Hz, 1H), 7.94 (dd, J=2.3, 9.1 Hz, 1H), 7.89 (s, 1H), 7.87 (s, 1H), 7.67 (d, J=8.8 Hz, 2H), 7.35 (dd, J=8.6, 8.6 Hz, 1H), 7.06 (dd, J=8.7, 8.7 Hz, 3H), 3.98 (s, 3H), 3.88 (dd, J=5.1, 5.1 Hz, 4H), 3.27 (dd, J=5.3, 5.3 Hz, 4H). LC-MS: Rt=3.29 min, m/z=432 [M+H].sup.+.

Example 161

N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)isonicotinamide

(689) ##STR00275##

(690) Yield: 32 mg.

(691) .sup.1H NMR (400 MHz, DMSO): δ 10.34 (s, 1H), 8.80-8.77 (m, 2H), 8.53 (d, J=2.1 Hz, 1H), 7.92-7.85 (m, 3H), 7.66 (d, J=9.2 Hz, 2H), 7.03 (d, J=9.2 Hz, 3H), 3.84 (dd, J=5.1, 5.1 Hz, 4H), 3.24 (dd, J=5.1, 5.1 Hz, 4H). LC-MS: Rt=2.89 min, m/z=385 [M+H].sup.+.

Example 162

N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-5-methoxypicolinamide

(692) ##STR00276##

(693) Yield: 36 mg.

(694) .sup.1H NMR (400 MHz, DMSO): δ 10.29 (s, 1H), 8.53 (d, J=2.0 Hz, 1H), 8.38 (d, J=2.6 Hz, 1H), 8.12 (d, J=9.0 Hz, 1H), 7.89 (dd, J=2.4, 9.0 Hz, 1H), 7.77 (d, J=9.2 Hz, 2H), 7.62 (dd, J=2.9, 8.8 Hz, 1H), 7.01 (dd, J=8.7, 8.7 Hz, 3H), 3.94 (s, 3H), 3.84 (dd, J=5.1, 5.1 Hz, 4H), 3.25-3.18 (m, 4H). LC-MS: Rt=3.43 min, m/z=415 [M+H].sup.+.

Example 163

N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-3-fluoro-4-methoxybenzamide

(695) ##STR00277##

(696) Yield: 33 mg.

(697) .sup.1H NMR (400 MHz, DMSO): δ 9.99 (s, 1H), 7.86 (s, 1H), 7.83 (s, 1H), 7.63 (dd, J=3.8, 9.0 Hz, 4H), 7.31 (dd, J=8.6, 8.6 Hz, 1H), 7.11 (d, J=9.2 Hz, 2H), 7.01 (d, J=9.2 Hz, 2H), 3.94 (s, 3H), 3.52 (dd, J=5.1, 5.1 Hz, 4H), 3.26 (dd, J=5.1, 5.1 Hz, 4H). LC-MS: Rt=3.42 min, m/z=431 [M+H].sup.+.

Example 164

4-Cyano-N-(4-(4-(5-cyanopyridin-2-yl)piperazin-1-yl)phenyl)benzamide

(698) ##STR00278##

(699) Yield: 27 mg.

(700) .sup.1H NMR (400 MHz, DMSO): δ 10.32 (s, 1H), 8.53 (d, J=2.0 Hz, 1H), 8.11 (d, J=8.5 Hz, 2H), 8.03 (d, J=8.5 Hz, 2H), 7.90 (dd, J=2.4, 9.0 Hz, 1H), 7.66 (d, J=9.0 Hz, 2H), 7.02 (d, J=9.0 Hz, 3H), 3.84 (dd, J=5.1, 5.1 Hz, 4H), 3.24 (dd, J=5.2, 5.2 Hz, 4H). LC-MS: Rt=3.29 min, m/z=409 [M+H].sup.+.

Example 165

N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)pyrimidine-4-carboxamide

(701) ##STR00279##

(702) Yield: 34 mg.

(703) .sup.1H NMR (400 MHz, DMSO): δ 10.69 (s, 1H), 9.42 (d, J=1.4 Hz, 1H), 9.13 (d, J=5.1 Hz, 1H), 8.13 (dd, J=1.4, 5.1 Hz, 1H), 7.81 (d, J=9.2 Hz, 2H), 7.63 (d, J=9.0 Hz, 2H), 7.11 (d, J=9.0 Hz, 2H), 7.03 (d, J=9.2 Hz, 2H), 3.52 (dd, J=5.1, 5.1 Hz, 4H), 3.29 (dd, J=5.1, 5.1 Hz, 4H). LC-MS: Rt=3.34 min, m/z=385 [M+H].sup.+.

Example 166

N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-5-methoxypicolinamide

(704) ##STR00280##

(705) Yield: 22 mg.

(706) .sup.1H NMR (400 MHz, DMSO): δ 10.30 (s, 1H), 8.39 (d, J=2.6 Hz, 1H), 8.12 (d, J=8.7 Hz, 1H), 7.77 (d, J=9.0 Hz, 2H), 7.64-7.60 (m, 3H), 7.11 (d, J=9.2 Hz, 2H), 7.01 (d, J=9.2 Hz, 2H), 3.94 (s, 3H), 3.51 (dd, J=5.1, 5.1 Hz, 4H), 3.26 (dd, J=5.1, 5.1 Hz, 4H). LC-MS: Rt=3.52 min, m/z=414 [M+H].sup.+.

Example 167

N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-4-methoxy-3-methylbenzamide

(707) ##STR00281##

(708) Yield: 45 mg.

(709) .sup.1H NMR (400 MHz, DMSO): δ 9.88 (s, 1H), 7.84 (dd, J=2.2, 8.5 Hz, 1H), 7.80 (d, J=1.8 Hz, 1H), 7.67-7.61 (m, 4H), 7.11 (d, J=9.2 Hz, 2H), 7.06 (d, J=8.7 Hz, 1H), 7.00 (d, J=9.2 Hz, 2H), 3.88 (s, 3H), 3.51 (dd, J=5.1, 5.1 Hz, 4H), 3.25 (dd, J=5.1, 5.1 Hz, 4H), 2.23 (s, 3H). LC-MS: Rt=3.52 min, m/z=427 [M+H].sup.+.

Example 168

N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-4-methoxy-2-methylbenzamide

(710) ##STR00282##

(711) Yield: 39 mg.

(712) .sup.1H NMR (400 MHz, DMSO): δ 9.95 (s, 1H), 7.65-7.60 (m, 4H), 7.43 (d, J=8.3 Hz, 1H), 7.11 (d, J=9.2 Hz, 2H), 6.99 (d, J=9.2 Hz, 2H), 6.87-6.83 (m, 2H), 3.80 (s, 3H), 3.51 (dd, J=5.1, 5.1 Hz, 4H), 3.23 (dd, J=5.1, 5.1 Hz, 4H), 2.40 (s, 3H). LC-MS: Rt=3.39 min, m/z=427 [M+H].sup.+.

Example 169

N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-3,4-dimethoxybenzamide

(713) ##STR00283##

(714) Yield: 52 mg.

(715) .sup.1H NMR (400 MHz, DMSO): δ 9.91 (s, 1H), 7.66-7.60 (m, 5H), 7.54 (d, J=2.0 Hz, 1H), 7.10 (dd, J=8.9, 11.9 Hz, 3H), 7.01 (d, J=9.2 Hz, 2H), 3.85 (d, J=3.1 Hz, 6H), 3.52 (dd, J=5.1, 5.1 Hz, 4H), 3.26 (dd, J=5.1, 5.1 Hz, 4H). LC-MS: Rt=3.30 min, m/z=443 [M+H].sup.+.

Example 170

N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-methoxy-3-methylbenzamide

(716) ##STR00284##

(717) Yield: 37 mg.

(718) .sup.1H NMR (400 MHz, DMSO): δ 9.88 (s, 1H), 8.53 (d, J=2.4 Hz, 1H), 7.90 (dd, J=2.4, 9.0 Hz, 1H), 7.84 (dd, J=2.1, 8.5 Hz, 1H), 7.79 (d, J=1.8 Hz, 1H), 7.64 (d, J=9.0 Hz, 2H), 7.07-6.98 (m, 4H), 3.88 (s, 3H), 3.84 (dd, J=5.1, 5.1 Hz, 4H), 3.24-3.17 (m, 4H), 2.23 (s, 3H). LC-MS: Rt=3.45 min, m/z=428 [M+H].sup.+.

Example 171

N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-6-methoxynicotinamide

(719) ##STR00285##

(720) Yield: 34 mg.

(721) .sup.1H NMR (400 MHz, DMSO): δ 10.08 (s, 1H), 8.78 (d, J=2.4 Hz, 1H), 8.53 (d, J=2.4 Hz, 1H), 8.23 (dd, J=2.5, 8.7 Hz, 1H), 7.90 (dd, J=2.3, 9.1 Hz, 1H), 7.63 (d, J=9.0 Hz, 2H), 7.02 (dd, J=6.5, 9.0 Hz, 3H), 6.95 (d, J=8.7 Hz, 1H), 3.95 (s, 3H), 3.84 (dd, J=5.1, 5.1 Hz, 4H), 3.23 (dd, J=5.1, 5.1 Hz, 4H). LC-MS: Rt=3.24 min, m/z=415 [M+H].sup.+.

Example 172

Methyl 6-(4-(4-(4-methoxybenzamido)phenyl)piperazin-1-yl)nicotinate

(722) ##STR00286##

(723) 4-Methoxy-N-(4-(piperazin-1-yl)phenyl)benzamide (96 mg, 0.25 mmol), methyl 6-bromopyridine-3-carboxylate (1.1 eq.) and DIPEA (5 eq., 161.3 mg, 1.25 mmol) were combined in a reaction tube. NMP (1 ml) was then added, the reaction tube flushed with nitrogen, sealed and the reaction mixture was stirred at 120° C. for 2.5 h. After completion the reaction mixture was cooled to rt and H.sub.2O added. The precipitate formed was collected by filtration, washed with H.sub.2O and dried. The product was triturated with Et2O/MeOH (95:5). The resulting material was dried in vacuo to afford the title compound. Yield 81 mg.

(724) .sup.1H NMR (400 MHz, DMSO): δ 9.46 (s, 1H), 8.70 (d, J=2.0 Hz, 1H), 8.02-7.92 (m, 3H), 7.61 (d, J=8.9 Hz, 2H), 7.03 (d, J=8.8 Hz, 2H), 6.96 (d, J=8.9 Hz, 2H), 6.87 (d, J=9.0 Hz, 1H), 3.88-3.83 (m, 9H), 3.29 (dd, J=5.2, 5.2 Hz, 4H), 2.81 (bs, 4H). LC-MS: Rt=3.70 min, m/z=447 [M+H].sup.+.

General Synthesis Sub-Series 3

(725) ##STR00287##

5-(4-(4-Nitrophenyl)piperazin-1-yl)picolinonitrile

(726) ##STR00288##

(727) 1-(4-Nitrophenyl)piperazine (622 mg, 3.0 mmol), 5-bromopicolinonitrile (500 mg, 2.73 mmol), Cs.sub.2CO.sub.3 (1.78 g, 5.46 mmol) and RuPhos (255 mg, 0.55 mmol) were suspended in anhydrous dioxane (15 ml) and degassed for 5 min with nitrogen. [Pd(OAc).sub.2] (61 mg, 0.27 mmol) was then added, the mixture further degassed (3 min) and the reaction vessel was sealed and heated at 90° C. for 4 h. After cooling to rt H.sub.2O was added and the resulting precipitate collected by filtration. The precipitate was washed with H.sub.2O (3×) and diethyl ether (3×) and dried to give the title compound (800 mg, 94%) as a yellow solid.

(728) .sup.1H NMR (400 MHz, DMSO): δ 8.49 (d, J=3.0 Hz, 1H), 8.15 (d, J=9.3 Hz, 2H), 7.84 (d, J=8.8 Hz, 1H), 7.43 (dd, J=3.0, 9.1 Hz, 1H), 7.10 (d, J=9.3 Hz, 2H), 3.73 (dd, J=5.8, 13.4 Hz, 8H). LC-MS: Rt=1.52 min, m/z=310 [M+H].sup.+.

5-(4-(4-Aminophenyl)piperazin-1-yl)picolinonitrile

(729) ##STR00289##

(730) 5-(4-(4-Nitrophenyl)piperazin-1-yl)picolinonitrile (830 mg, 2.68 mmol) was suspended in EtOH (32 ml) and H.sub.2O (8 ml), NH.sub.4Cl (86 mg, 1.61 mmol) was added and the mixture heated at 40° C. Iron powder (0.9 g, 16.1 mmol) was then added and the mixture was stirred at 90° C. for 2 h. Additional iron powder (450 mg, 8.0 mmol) was added and stirring continued at 95° C. for 5 h. After cooling to rt the reaction mixture was filtered and partitioned between DCM and saturated NaHCO.sub.3. The aqueous phase was extracted with DCM (3×) and the combined organic phases dried (Na.sub.2SO.sub.4), filtered and evaporated. The residue was re-dissolved in chloroform and evaporated (3×) to provide the title compound (705 mg, 94%) as a dark solid.

(731) .sup.1H NMR (400 MHz, DMSO): δ 8.52 (d, J=2.8 Hz, 1H), 7.82 (d, J=8.6 Hz, 1H), 7.47 (dd, J=3.0, 9.1 Hz, 1H), 6.81 (d, J=8.8 Hz, 2H), 6.59-6.55 (m, 2H), 4.67 (s, 2H), 3.58 (dd, J=5.1, 5.1 Hz, 4H), 3.09 (dd, J=5.1, 5.1 Hz, 4H). LC-MS: Rt=1.27 min, m/z=280 [M+H].sup.+.

Example 173

N-(4-(4-(6-Cyanopyridin-3-yl)piperazin-1-yl)phenyl)-5-methoxypicolinamide

(732) ##STR00290##

(733) To a solution of 5-methoxypicolinic acid (1.1 eq., 36 mg, 236 μmol) in anhydrous DMF (2.5 ml) and DIPEA (1.5 eq., 56 μL, 322 μmol) was added HATU (1.2 eq., 98 mg, 258 μmol) and the reaction mixture was stirred for 20 min at rt. 5-(4-(4-Aminophenyl)piperazin-1-yl)picolinonitrile (60 mg, 215 μmol) was then added and the reaction was stirred at rt overnight. H.sub.2O was then added and the resulting precipitate collected by filtration. The precipitate was washed with H.sub.2O (3×) and diethyl ether (3×) and dried. The crude solid was dissolved in DCM/MeOH (2:1), adsorbed onto HM-N beads (Biotage) and evaporated. The resulting material was dry-loaded onto a silica column and purified by flash column chromatography eluting with 0.5 to 3% methanol/dichloromethane to afford the title compound (31 mg, 35%) as a yellow solid.

(734) .sup.1H NMR (400 MHz, DMSO): δ 10.34 (s, 1H), 8.55 (d, J=2.8 Hz, 1H), 8.43 (d, J=2.8 Hz, 1H), 8.16 (d, J=8.6 Hz, 1H), 7.82 (dd, J=7.5, 8.7 Hz, 3H), 7.66 (dd, J=2.9, 8.7 Hz, 1H), 7.50 (dd, J=3.0, 9.1 Hz, 1H), 7.06 (d, J=9.1 Hz, 2H), 3.99 (s, 3H), 3.63 (dd, J=5.2, 5.2 Hz, 4H), 3.32 (dd, J=5.1, 5.1 Hz, 4H). LC-MS: Rt=3.80 min, m/z=415 [M+H].sup.+.

Example 174

N-[4-[4-(5-Cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-prop-2-ynoxy-benzamide

(735) ##STR00291##

(736) A solution of 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-3-carbonitrile (Example 50, step a) (250 mg, 0.890 mmol), 4-prop-2-ynoxybenzoic acid (CAS Nr. 21926-55-6) (158 mg, 0.890 mmol), O-(7-azabenzotriazol-1-yl)-N,N,N,N-tetramethyluronium hexafluorophosphate (374 mg, 0.980 mmol) and triethylamine (0.25 mL, 1.79 mmol) in DMF (10 mL) was stirred at 25° C. for 16 h. The reaction was quenched with H.sub.2O (20 mL). The solid was filtered and washed with EtOH (10 mL). The resulting solid was crystallized from DMSO/EtOH (25 mL/80 mL)) to afford the N-[4-[4-(5-cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-prop-2-ynoxy-benzamide (209 mg, 52%) as pink solid. LC-MS: m/z=438.2 [M+H].sup.+.

Example 175

N-[4-[4-(5-Cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-(2-prop-2-ynoxyethoxy)benzamide

(737) ##STR00292##

(738) A solution of 6-[4-(4-aminophenyl)piperazin-1-yl]pyridine-3-carbonitrile (Example 50, step a) (250 mg, 0.890 mmol), 4-(2-prop-2-ynoxyethoxy)benzoic acid (CAS Nr. 1153245-98-7) (197 mg, 0.890 mmol), O-(7-azabenzotriazol-1-yl)-N,N,N,N-tetramethyluronium hexafluorophosphate (374 mg, 0.980 mmol) and triethylamine (0.31 mL, 2.24 mmol) in DMF (15 mL) was stirred at 25° C. for 16 h. The reaction was quenched with H.sub.2O (35 mL). The resulting solid was collected by filtration and recrystallized from DMSO/EtOH (5 mL/10 mL). The solid was collected, washed with EtOH (50 mL) and dried under vacuum to afford N-[4-[4-(5-cyano-2-pyridyl)piperazin-1-yl]phenyl]-4-(2-prop-2-ynoxyethoxy)benzamide (140 mg, 32%) as the pink solid. LC-MS: m/z=482.2 [M+H].sup.+.

Example 176

N-[4-[4-(5-Ethynyl-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide

(739) ##STR00293##

a) tert-Butyl 4-(5-ethynyl-2-pyridyl)piperazine-1-carboxylate

(740) ##STR00294##

(741) A solution of 5-ethynyl-2-fluoro-pyridine (500 mg, 4.13 mmol), 1-Boc-piperazine (923 mg, 4.95 mmol) and triethylamine (1.15 mL, 8.26 mmol) in MeCN (10 mL) was stirred at 60° C. for 16 h. The reaction was poured into H.sub.2O (50 mL) and extracted with EtOAc (70 mL). The organic layer was separated, dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The residue was purified by silica gel chromatography (petroleum ehter:EtOAc, 10:1 to 2:1) to afford tert-butyl 4-(5-ethynyl-2-pyridyl)piperazine-1-carboxylate (630 mg, 79%) as white solid. .sup.1H NMR (CHLOROFORM-d, 400 MHz) δ 8.24 (d, 1H, J=2.2 Hz), 7.48 (dd, 1H, J=2.3, 8.9 Hz), 6.48 (d, 1H, J=8.8 Hz), 3.4-3.5 (m, 8H), 3.00 (s, 1H), 1.41 (s, 9H).

b) 1-(5-Ethynyl-2-pyridyl)piperazine hydrochloride

(742) ##STR00295##

(743) To a solution at 25° C. of tert-butyl 4-(5-ethynyl-2-pyridyl)piperazine-1-carboxylate (600 mg, 2.09 mmol) in EtOAc (10 mL) was added dropwise HCl in dioxane (10.4 mL, 41.76 mmol). The resulting mixture was stirred for 16 h. The reaction solution was concentrated under vacuum and the resulting solid was collected and was washed with EtOAc (20 mL) to afford 1-(5-ethynyl-2-pyridyl)piperazine hydrochloride (422 mg, 70%) as white solid. LC-MS: m/z=188.1 [M+H].sup.+.

c) 1-(5-Ethynyl-2-pyridyl)-4-(4-nitrophenyl)piperazine

(744) ##STR00296##

(745) A solution of 1-(5-ethynyl-2-pyridyl)piperazine (460 mg, 2.46 mmol), 4-fluoronitrobenzene (347 mg, 2.46 mmol), and potassium carbonate (849 mg, 6.14 mmol) in DMSO (80 mL) was stirred at 90° C. for 1.5 h. The reaction solution was poured into H.sub.2O (300 mL) and the solid was collected by filtration and washed with THF (20 mL) to afford 1-(5-ethynyl-2-pyridyl)-4-(4-nitrophenyl)piperazine (460 mg, 50%) as light yellow solid. LC-MS: m/z=309.0 [M+H].sup.+.

d) 4-[4-(5-Ethynyl-2-pyridyl)piperazin-1-yl]aniline

(746) ##STR00297##

(747) To a solution of 1-(5-ethynyl-2-pyridyl)-4-(4-nitrophenyl)piperazine (430 mg, 1.39 mmol) and NH.sub.4Cl (1.48 g, 27.9 mmol) in MeOH (20 mL) was added Zn (1.82 g, 27.9 mmol) and the mixture was stirred at 25° C. for 4 h. The reaction was filtered through Celite. The filtrate was concentrated under vacuum. The residue was washed with H.sub.2O (50 mL), and the solid was collected to afford 4-[4-(5-ethynyl-2-pyridyl)piperazin-1-yl]aniline (282 mg, 62%) as yellow solid. LC-MS: m/z=279.1 [M+H].sup.+.

e) N-[4-[4-(5-Ethynyl-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide

(748) A solution of 4-[4-(5-ethynyl-2-pyridyl)piperazin-1-yl]aniline (200 mg, 0.720 mmol), 4-methoxybenzoic acid (109 mg, 0.720 mmol), 0-(7-azabenzotriazol-1-yl)-N,N,N′N′-tetramethyluronium hexafluorophosphate (328 mg, 0.860 mmol) and triethylamine (0.3 mL, 2.16 mmol) in DMF (9 mL) was stirred at 25° C. for 16 h. The reaction was filtered through Celite. The filtrate was purified by two consecutive preparative HPLCs (HCl.sub.aq. as additive, then TFA.sub.aq.) to afford N-[4-[4-(5-ethynyl-2-pyridyl)piperazin-1-yl]phenyl]-4-methoxy-benzamide (41 mg, 13%) as yellow solid. LC-MS: m/z=413.2 [M+H].sup.+.

Example 177

4-Prop-2-ynoxy-N-[4-[4-(2-pyridyl)piperazin-1-yl]phenyl]benzamide

(749) ##STR00298##

(750) A solution of 4-[4-(2-pyridyl)piperazin-1-yl]aniline (Example 1, step b) (260 mg, 1.02 mmol), 4-prop-2-ynoxybenzoic acid (CAS Nr. 21926-55-6) (180 mg, 1.02 mmol), 0-(7-azabenzotriazol-1-yl)-N,N,N,N-tetramethyluronium hexafluorophosphate (428 mg, 1.12 mmol) and triethylamine (0.28 mL, 2.04 mmol) in DMF (10 mL) was stirred at 25° C. for 16 h. The reaction was quenched with H.sub.2O (20 mL). The resulting solid was filtered and washed with EtOH (10 mL) before purification by Prep-HPLC (TFA as additive) to afford 4-prop-2-ynoxy-N-[4-[4-(2-pyridyl)piperazin-1-yl]phenyl]benzamide (62 mg, 15%) as pink solid. LCMS: m/z=413.2 [M+H].sup.+.

Example 178

4-(2-Prop-2-ynoxyethoxy)-N-[4-[4-(2-pyridyl)piperazin-1-yl]phenyl]benzamide

(751) ##STR00299##

(752) A solution of 4-(2-prop-2-ynoxyethoxy)benzoic acid (CAS Nr. 1153245-98-7) (260 mg, 1.18 mmol), 4-[4-(2-pyridyl)piperazin-1-yl]aniline (300.0 mg, 1.18 mmol), 0-(7-azabenzotriazol-1-yl)-N,N,N,N-tetramethyluronium hexafluorophosphate (493 mg, 1.3 mmol) and triethylamine (0.33 mL, 2.36 mmol) in DMF (10 mL) was stirred at 25° C. for 16 h. The reaction was quenched with H.sub.2O (20 mL). The resulting solid was collected by filtration and washed with EtOH (10 mL). The crude product was re-crystallized from DMSO/EtOH (25 mL/80 mL) to afford 4-(2-prop-2-ynoxyethoxy)-N-[4-[4-(2-pyridyl)piperazin-1-yl]phenyl]benzamide (52 mg, 9%) as pink solid. LC-MS: m/z=457.3 [M+H].sup.+.

(753) Tritiation Procedures

(754) General Methods

(755) Reactions with tritium gas were performed on a stainless steel manifold purchased from RC Tritec AG. Liquid scintillation counting for tritium compounds was accomplished using a HIDEX 300 SL and ULTIMATE GOLD cocktail (PerkinElmer Inc., Waltham, Mass., USA). Pre-coated thin-layer chromatography sheets (TLC) were obtained from Merck KGaA (Darmstadt, Germany). Developed plates were visualized using an automatic TLC linear analyzer (Berthold Technologies, Bad Wildbad, Germany). Radiochemical purity was measured using the β-radioactivity HPLC detector RAMONA with internal solid scintillator (Raytest, Straubenhardt, Germany). Molar activity was determined by mass spectrometric isotopic peak intensity distribution, using 4000QTRAP system (AB Sciex GmbH, Zug, CH), flow injection mode with a CTC PAL, and an Agilent 1100 microLC pump without any separation.

2-Fluoro-4-[.SUP.3.H.SUB.3.]methoxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide ([.SUP.3.H]Example 1)

(756) ##STR00300##

(757) [.sup.3H]Methyl nosylate (152 μg, 1.85 GBq=50 mCi, 0.68 μmol), dissolved in 1 ml Tol, was transferred to a 5 ml reactor and concentrated under a stream of Ar to dryness. A solution of 2-fluoro-4-hydroxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (785 μg, 2.0 μmol) in THF (0.4 ml) and Cs.sub.2CO.sub.3 (543 μg, 1.67 μmol) were added. The reactor was tightly closed, and the reaction mixture was stirred for 2.5 h at 50° C. The reaction mixture was filtered through a 0.22 μm membrane filter and purified by preparative HPLC (XBridge C18, 5 μm, 10 mm×250 mm) using MeCN/H.sub.2O (70:30) as eluent (isocratic, run time 15 min) at a flow rate of 8 ml/min. An amount of 433 MBq (11.7 mCi) of the desired compound was obtained with a radiochemical purity of 99% and a molar activity of 2.7 TBq/mmol (73 Ci/mmol). The identity of the labeled compound was confirmed by MS and by co-injection of the cold reference standard with the radiolabeled material. MS m/z: 407.2 [M(H)+H].sup.+ (5%), 409.2 [M(.sup.3H)+H].sup.+ (3%), 411.2 [M(.sup.3H.sub.2)+H].sup.+ (24%), 413.2 [M(.sup.3H.sub.3)+H].sup.+ (68%).

4-[.SUP.3.H.SUB.3.] Methoxy-N-[4-(4-pyridin-2-ylpiperazin-1-yl)phenyl]benzamide ([.SUP.3.H]Example 3)

(758) ##STR00301##

(759) A solution of [.sup.3H]methyl nosylate (143 μg, 1.85 GBq=50 mCi, 0.64 μmol) in 5 ml Tol was transferred to a 5 ml reactor and concentrated under a stream of Ar to dryness. A solution of 4-hydroxy-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide (Example 2) (810 μg, 2.16 μmol) in THF (0.5 ml) and Cs.sub.2CO.sub.3 (460 μg, 1.41 μmol) were added. The reactor was tightly closed, and the reaction mixture was stirred for 16 h at 45° C. The reaction mixture was diluted with 1 ml MeCN/H.sub.2O 1:1, filtered through a 0.22 μm membrane filter and purified by preparative HPLC (XBridge C18, 5 μm, 10 mm×250 mm) using 0.1 M ammonia formiate buffer, pH 9/MeCN/H.sub.2O as eluent (isocratic 4 min: 1:1:8; gradient from 1:1:8 to 1:9:0 in 16 min) at a flow rate of 6 ml/min. An amount of 292 MBq (7.9 mCi) of the desired compound was obtained with a radiochemical purity of 96% and a molar activity of 2.9 TBq/mmol (78 Ci/mmol). The identity of the labeled compound was confirmed by MS and by co-injection of the cold reference standard with the radiolabeled material. MS m/z: 393.4 [M(.sup.3H.sub.2)+H].sup.+ (13%), 395.4 [M(.sup.3H.sub.3)+H].sup.+ (87%).

[.SUP.3.H]4-(2-(2-Fluoroethoxy)ethoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide ([.SUP.3.H]Example 12)

(760) ##STR00302##

(761) In a 4 ml tritiation flask, 4-(2-(2-fluoroethoxy)ethoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl) benzamide (Example 12) (2.0 mg, 4.31 μmol) and Kerr's catalyst ([Ir(Im-Mes)(PPhMe.sub.2)(COD)]PF.sub.6) (5.73 mg, 6.46 μmol) were dissolved in DMF (1 ml). The flask was attached to a RC Tritec tritium manifold and degassed by three freeze-thaw cycles. Tritium gas was introduced, and the light orange solution was vigorously stirred for 4 h in an atmosphere of tritium at 500 mbar. The solution was cooled by liquid nitrogen and the excess tritium gas in the reaction vessel was reabsorbed on a uranium trap for waste-tritium. The solvent was lyophilized off, and labile tritium was removed by lyophilization with a 9:1 mixture of EtOH and H.sub.2O (3×1 ml) and Tol (2×1 ml). The remaining yellow oil was dissolved in DCM (0.3 ml), transferred in a 50 ml flask and the solution was diluted with 9 ml MeOH. Metal scavenger MP-TMT (macroporous polystyrene-bound trimercaptotriazine, Biotage, Uppsala, Sweden, 89.4 mg, load: 0.65 mmol/g, 58.1 μmol) was added and the mixture was shaken over night at room temperature. The scavenger was removed by filtering through a 0.45 m membrane filter. The crude product was purified by preparative HPLC (XBridge Prep, 5 μm, 10 mm×250 mm) using acetonitrile+0.01% TFA/water+0.01% TFA as eluent (gradient 1-15 min from 1:9 to 8:2, run time 17 min) at a flow rate of 7 ml/min. An amount of 148MBq (4 mCi) of the title compound was obtained with a radiochemical purity of 98% and a molar activity of 2.6 TBq/mmol (71.3 Ci/mmol), determined by MS spectrometry. The identity of the labeled compound was confirmed by MS and by co-injection of the cold reference standard with the radiolabeled material. MS: m/z=465.4 [M(H)+H].sup.+ (7%), 467.4 [M(.sup.3H)+H].sup.+ (19%), 469.4 [M(.sup.3H.sub.2)+H].sup.+ (28%), 471.4 [M(.sup.3H.sub.3)+H].sup.+ (24%), 473.4 [M(.sup.3H.sub.4)+H].sup.+ (14%) 475.4 [M(.sup.3H.sub.5)+H].sup.+ (5%), 467.4 [M(.sup.3H.sub.6)+H].sup.+ (3%).

N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-[.SUP.3.H.SUB.3.]methoxybenzamide ([.SUP.3.H]Example 50)

(762) ##STR00303##

(763) A solution of [.sup.3H]methyl nosylate (137 μg, 1.85 GBq=50 mCi, 0.62 μmol) in 5 ml Tol was transferred to a 5 ml round-bottomed flask and concentrated under a stream of Ar to dryness. A solution of N-(4-(4-(5-cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-hydroxybenzamide (Example 108) (1 mg, 2.50 μmol) in DMSO (0.5 ml) and Cs.sub.2CO.sub.3 (800 μg, 2.46 μmol) were added. The reactor was tightly closed, and the reaction mixture was stirred for 2 h at 70° C. The reaction mixture was diluted with 2 ml MeOH, filtered through a 500 mg SPE-HCO.sub.3 cartridge (Agilent Technologies, Santa Clara, Calif., USA), washed with 10 ml MeOH and purified by preparative HPLC (XBridge C18, 5 μm, 10 mm×250 mm) using MeCN and H.sub.2O as eluent (isocratic 3 min: 1:3; gradient from 1:3 to 3:2 in 15 min) at a flow rate of 6 ml/min. An amount of 163 MBq (4.4 mCi) of the desired compound was obtained with a radiochemical purity of 99% and a molar activity of 3.0 TBq/mmol (81 Ci/mmol). The identity of the labeled compound was confirmed by MS and by co-injection of the cold reference standard with the radiolabeled material. MS m/z: 414.3 [M(H)+H].sup.+ (3%), 416.3 [M(.sup.3H)+H]+(2%), 418.3 [M(.sup.3H.sub.2)+H].sup.+ (5%), 420.3 [M(.sup.3H.sub.3)+H].sup.+ (90%).

[.SUP.3.H]N-(4-(4-(5-Cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-(2-(2-fluoroethoxy)ethoxy)benzamide ([.SUP.3.H]Example 121)

(764) ##STR00304##

(765) In a 4 ml tritiation flask, N-(4-(4-(5-cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-(2-(2-fluoroethoxy)ethoxy)benzamide (Example 121) (2.0 mg, 4.09 μmol) and Crabtree's catalyst ([Ir(COD)(PCy.sub.3)(Py)]PF.sub.6) (4.32 mg, 5.31 μmol) were dissolved in DCM (1.0 ml). The reaction and the purification were performed in analogy to [.sup.3H]4-(2-(2-fluoroethoxy)ethoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide ([.sup.3H]Example 12) to provide 3.48 GBq (94 mCi) of the desired compound with a radiochemical purity of 98% and a molar activity of 3.81 TBq/mmol (103 Ci/mmol). The identity of the labeled compound was confirmed by MS and by co-injection of the cold reference standard with the radiolabeled material. MS m/z: 490.2 [M(H)+H].sup.+ (2%), 492.2 [M(.sup.3H)+H].sup.+ (3%), 494.2 [M(.sup.3H.sub.2)+H].sup.+ (8%), 496.2 [M(.sup.3H.sub.3)+H].sup.+ (26%), 498.2 [M(.sup.3H.sub.4)+H].sup.+ (46%), 500.2 [M(.sup.3H.sub.5)+H].sup.+ (15%).

[.SUP.3.H]N-(4-(4-(4-Cyanophenyl)piperazin-1-yl)phenyl)-4-(2-(2-fluoroethoxy)ethoxy)benzamide ([.SUP.3.H]Example 122)

(766) ##STR00305##

(767) In a 4 ml tritiation flask, N-(4-(4-(4-cyanophenyl)piperazin-1-yl)phenyl)-4-(2-(2-fluoroethoxy)ethoxy) benzamide (Example 122) (2.0 mg, 7.8 μmol) and Kerr's catalyst ([Ir(Im-Mes)(PPhMe.sub.2)(COD)]PF.sub.6) (4.82 mg, 5.32 μmol) were dissolved in DCM (1.0 ml). The reaction and the purification were performed in analogy to [.sup.3H]4-(2-(2-fluoroethoxy)ethoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide ([.sup.3H]Example 12) to provide 777 GBq (21 mCi) of the desired compound with a radiochemical purity of 99% and a molar activity of 1.96 TBq/mmol (52.9 Ci/mmol). The identity of the labeled compound was confirmed by MS and by co-injection of the cold reference standard with the radiolabeled material. MS m/z: 491.4 [M(.sup.3H)+H].sup.+ (4%), 493.4 [M(.sup.3H.sub.2)+H].sup.+ (11%), 495.4 [M(.sup.3H.sub.3)+H].sup.+ (34%), 497.4 [M(.sup.3H.sub.4)+H]±(51%).

[.SUP.3.H]4-(Fluoromethoxy)-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide ([.SUP.3.H]Example 134)

(768) ##STR00306##

(769) In a 4 ml tritiation flask, 4-(fluoromethoxy)-N-(4-(4-(pyridin-3-yl)piperazin-1-yl)phenyl)benzamide (Example 134) (4.66 mg, 11.5 μmol) and Crabtree's catalyst ([Ir(COD)(PCy.sub.3)(Py)]PF.sub.6) (14.51 mg, 18.0 μmol) were dissolved in chlorobenzene (0.8 ml). The reaction and the purification were performed in analogy to [.sup.3H]4-(2-(2-fluoroethoxy)ethoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide ([.sup.3H]Example 12), except for the reaction time of 3.5 h and the temperature that was increased to 90° C. 1.18 TBq (32 mCi) of the desired compound with a radiochemical purity of 98% and a molar activity of 1.66 TBq/mmol (44.9 Ci/mmol) were obtained. The identity of the labeled compound was confirmed by MS and by co-injection of the cold reference standard with the radiolabeled material. MS m/z: 407.2 [M(H)+H].sup.+ (49%), 409.2 [M(.sup.3H)+H].sup.+ (11%), 411.2 [M(.sup.3H.sub.2)+H].sup.+ (7%), 413.2 [M(.sup.3H.sub.3)+H].sup.+ (11%), 415.2 [M(.sup.3H.sub.4)+H].sup.+ (13%) 417.2 [M(.sup.3H.sub.5)+H].sup.+ (9%).

[.SUP.3.H]4-(Fluoromethoxy)-N-[4-(4-pyridin-2-ylpiperazin-1-yl)phenyl]benzamide ([.SUP.3.H]Example 135)

(770) ##STR00307##

(771) In a 4 ml tritiation flask, 4-(fluoromethoxy)-N-[4-(4-pyridin-2-ylpiperazin-1-yl)phenyl]benzamide (Example 135) (2.0 mg, 4.92 μmol) and Crabtree's catalyst ([Ir(COD)(PCy.sub.3)(Py)]PF.sub.6) (5.20 mg, 6.40 μmol) were dissolved in DCM (1.0 ml). The reaction and the purification were performed in analogy to [.sup.3H]4-(2-(2-fluoroethoxy)ethoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide ([.sup.3H]Example 12) to provide 3.33 TBq (90 mCi) of the desired compound with a radiochemical purity of 99% and a molar activity of 5.44 TBq/mmol (147 Ci/mmol). The identity of the labeled compound was confirmed by MS and by co-injection of the cold reference standard with the radiolabeled material. MS m/z: 407.2 [M(H)+H].sup.+ (2%), 409.2 [M(.sup.3H)+H].sup.+ (1%), 411.2 [M(.sup.3H.sub.2)+H].sup.+ (1%), 413.2 [M(.sup.3H.sub.3)+H].sup.+ (6%), 415.2 [M(.sup.3H.sub.4)+H].sup.+ (15%), 417.2 [M(.sup.3H.sub.5)+H].sup.+ (37%), 419.2 [M(.sup.3H.sub.6)+H].sup.+ (31%), 417.2 [M(.sup.3H.sub.7)+H].sup.+ (7%).

[.SUP.3.H]N-[4-[4-(5-Cyanopyridin-2-yl)piperazin-1-yl]phenyl]-4-(fluoromethoxy)benzamide ([.SUP.3.H]Example 136)

(772) ##STR00308##

(773) In a 4 ml tritiation flask, N-(4-(4-(5-cyanopyridin-2-yl)piperazin-1-yl)phenyl)-4-(fluoromethoxy) benzamide (Example 136) (2.0 mg, 4.64 μmol) and Crabtree's catalyst ([Ir(COD)(PCy.sub.3)(Py)]PF.sub.6) (4.90 mg, 6.03 μmol) were dissolved in DCM (1.0 ml). The reaction and the purification were performed in analogy to [.sup.3H]4-(2-(2-fluoroethoxy)ethoxy)-N-(4-(4-(pyridin-2-yl)piperazin-1-yl)phenyl)benzamide ([.sup.3H]Example 12) to provide 1.44 TBq (39 mCi) of the desired compound with a radiochemical purity of 99% and a molar activity of 3.55 TBq/mmol (96 Ci/mmol). The identity of the labeled compound was confirmed by MS and by co-injection of the cold reference standard with the radiolabeled material. MS m/z: 432.2 [M(H)+H].sup.+ (2%), 434.2 [M(.sup.3H)+H].sup.+ (3%), 436.2 [M(.sup.3H.sub.2)+H].sup.+ (16%), 438.2 [M(.sup.3H.sub.3)+H].sup.+ (36%), 440.2 [M(.sup.3H.sub.4)+H].sup.+ (30%), 442.2 [M(.sup.3H.sub.5)+H].sup.+ (9%), 444.2 [M(.sup.3H.sub.6)+H].sup.+ (4%).

(774) TABLE-US-00001 TABLE 1 Displacement assay results sel. counterscreen PCT_INHIB PCT_INHIB Example A30P AD No. @ 1 μM @ 1 μM 1 100 95 2 85 93 3 100% @ 3 μM 100% @ 3 μM 4 89 91 5 99 102 6 83 95 7 90 108 8 93 86 9 82 96 10 83 81 11 87 86 12 99 99 13 90 103 14 91 96 15 94 98 16 87 97 17 87 98 18 95 99 19 81 20 90 103 21 85 91 22 84 23 82 24 94 25 83 26 93 27 89 28 82 29 81 83 30 91 96 31 90 98 32 87 88 33 85 90 34 84 99 35 82 96 36 86 91 37 94 97 38 96 93 39 87 69 40 86 92 41 84 90 42 91 94 43 84 99 44 95 94 45 97 98 46 94 96 47 83 94 48 97 93 49 92 95 50 97 86 51 94 94 52 92 95 53 82 86 54 82 90 55 81 95 56 88 98 57 102 101 58 93 92 59 85 97 60 85 96 61 86 93 62 89 97 63 95 94 64 88 92 65 100 99 66 104 103 67 94 88 68 96 90 69 89 86 70 84 64 71 101 100 72 80 86 73 88 91 74 93 95 75 95 95 76 94 91 77 98 96 78 98 94 79 95 93 80 90 94 81 90 92 82 91 106 83 86 95 84 88 100 85 98 107 86 95 100 87 88 98 88 87 71 89 85 88 90 85 74 91 85 54 92 96 86 93 99 89 94 81 93 95 83 95 96 84 66 97 97 106 98 86 86 99 82 86 100 86 85 101 95 99 102 89 88 103 100 99 104 98 100 105 100 98 106 82 88 107 96 96 108 81 92 109 96 97 110 99 99 111 94 92 112 87 74 113 87 79 114 91 92 115 87 90 116 81 85 117 90 88 118 88 92 119 83 89 120 81 93 121 87 86 122 88 85 123 80 95 124 82 91 125 82 92 126 82 89 127 81 78 128 92 98 129 86 94 130 81 87 131 88 90 132 82 20 133 85 84 134 94 93 135 97 98 136 91 92 137 80 92 138 82 89 139 94 94 140 94 93 141 96 94 142 91 91 143 91 91 144 89 92 145 98 97 146 95 91 147 88 91 148 86 89 149 93 91 150 98 94 151 93 91 152 90 88 153 92 87 154 98 96 155 85 97 156 81 76 157 91 92 158 83 87 159 88 89 160 96 95 161 84 87 162 84 78 163 94 92 164 80 90 165 86 90 166 81 70 167 91 88 168 95 96 169 83 82 170 86 82 171 89 92 172 93 84 173 83 82 174 87 @ 3 μM 100 @ 3 μM 175 85 @ 3 μM 98 @ 3 μM 176 102 @ 3 μM 97 @ 3 μM 177 96 @ 3 μM 97 @ 3 μM 178 97 @ 3 μM 93 @ 3 μM