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公开(公告)号:DE1644428A1
公开(公告)日:1971-04-29
申请号:DE1644428
申请日:1965-04-17
Applicant: BASF AG
Inventor: WEIDINGER HANS DR , MOEBIUS LEANDER DR , EILINGSFELD HEINZ DR
IPC: C07D271/10 , C07D271/113 , C09B1/06 , C09B1/22 , C09B1/26 , C09B1/58 , C09B1/60
Abstract: The invention comprises dyes of the formula wherein X is amino, or alkylamino; Y is hydrogen, amino, alkylamino, hydroxy, piperidinyl or alkylmercapto; Z is a linear or branched chain alkyl of up to 8 carbon atoms which may bear alkoxy, cyano, unsubstituted or substituted carbamoyl or carbalkoxy groups, or denotes an aralkyl radical or the propinyl group. The compounds are prepared by reacting a carboxylic hydrazide of the formula where Z11 is No2 or as Y, either with CS2 in a alkaline reacting agent, and simultaneously or subsequently reacting with an alkylating agent which yields Z, or with a mercapto formamide chloride of the formula where R1 and R2 are substituted or unsubstitute alkyl or aryl radicals or together with the nitrogen form a piperidinyl or morpholino ring, and subsequently reducing the nitro group to an amino group. The mercapto formamide chloride may be formed in situ by treating a dithiocarbamic ester of the formula with chlorinating agents.
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公开(公告)号:CH451171A
公开(公告)日:1968-05-15
申请号:CH915665
申请日:1965-06-30
Applicant: BASF AG
Inventor: WEIDINGER HANS DR , EILINGSFELD HEINZ DR , MOEBIUS LEANDER DR
IPC: C07D271/10 , C07D271/113 , C09B1/06 , C09B1/22 , C09B1/26 , C09B1/58 , C09B1/60 , C07D85/54
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公开(公告)号:CH406131A
公开(公告)日:1966-08-15
申请号:CH616364
申请日:1964-05-12
Applicant: BASF AG
Inventor: WEIDINGER HANS DR , EILINGSFELD HEINZ DR , MOEBIUS LEANDER DR
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公开(公告)号:DE3062542D1
公开(公告)日:1983-05-05
申请号:DE3062542
申请日:1980-09-27
Applicant: BASF AG
Inventor: HICKMANN ECKHARD DR , OESER HEINZ-GUENTER DR , MOEBIUS LEANDER DR
IPC: C07D401/06 , A61K31/47 , C07D209/38 , C07D211/22 , C07D215/14 , C07D215/50
Abstract: The present invention relates to a simplified process, which avoids organo-lithium intermediates, for the preparation of erythro- alpha -piperid-2-yl-2,8-bis-(trifluoromethyl)-quinolin-4-yl-methanol, wherein 2,8-bis-(trifluoromethyl)-quinoline-4-carboxylic acid or a salt thereof is reacted with a pyrid-2-yl-magnesium halide to give pyrid-2-yl-2,8-bis-(trifluoromethyl)-quinolin-4-yl ketone in the manner of a Grignard reaction, and this product is hydrogenated, in a conventional manner, to give erythro- alpha -piperid-2-yl-2,8-bis-(trifluoromethyl)-quinolin-4-yl-methanol.
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