发明名称 |
VERFAHREN ZUR HERSTELLUNG VON 1-(6-METHYLPYRIDIN-3-YL)-2-[(4-(METHYLSULFONYL)PHENYL] ETHANON |
摘要 |
A five-step process for preparing 1-(6-methylpyridin-3-yl) -2-[(4-methylsulphonyl)phenyl] -ethanone of formula (I) described; characterized in that a) 4-(methylthio) benzyl alcohol is converted with hydrochloric acid into 4-(methylthio) benzyl chloride, b) 4-(methylthio) benzyl chloride is converted with an alkali metal cyanide into 4-(methylthio) phenylacetonitrile, c) 4-(methylthio) -phenylacetonitrile is condensed with a 6-methylnicotinic ester to give 3-[2- (4-methylthio) phenyl) -2-cyanoacetyl] (6-methyl) -pyridine, d) 3-[2-(4-methylthio) phenyl)-2-cyanoacetyl] (6-methyl) -pyridine is hydrolysed and decarboxylated under acidic conditions to give 3-[2-(4-methylthio) phenyl) acetyl] (6-methyl) pyridine and, e) 3-[2(4-(methylthio) phenyl) acetyl] (6-methyl) pyridine is oxidized to give the end product. The compound of formula (I) is an intermediate for preparing COX-2 inhibitors, pharmaceutically active compounds having analgesic and antiinflammatory action. |
申请公布号 |
DE60007133(T2) |
申请公布日期 |
2004.09.09 |
申请号 |
DE2000607133T |
申请日期 |
2000.07.17 |
申请人 |
LONZA AG, BASEL;MERCK & CO., INC. |
发明人 |
BESSARD, YVES;LERESCHE, EDWARD |
分类号 |
C07D213/50 |
主分类号 |
C07D213/50 |
代理机构 |
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代理人 |
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