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公开(公告)号:ZA7504430B
公开(公告)日:1976-06-30
申请号:ZA7504430
申请日:1975-07-10
Applicant: HOECHST AG
IPC: C07D211/02 , C07D211/76 , C07D
CPC classification number: C07D211/76 , C07D211/02
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公开(公告)号:ZA7501397B
公开(公告)日:1976-02-25
申请号:ZA7501397
申请日:1975-03-07
Applicant: HOECHST AG
Inventor: MUSIL J , BARTMANN W , GRANZER E , TEUFEL H
IPC: C07C20060101 , C07C255/34
CPC classification number: C07C255/00
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公开(公告)号:DK93775A
公开(公告)日:1975-09-10
申请号:DK93775
申请日:1975-03-07
Applicant: HOECHST AG
Inventor: TEUFEL H , BARTMANN W , GRANZER E , MUSIL J
IPC: C07C251/32 , A61K20060101 , A61K31/00 , A61K31/11 , A61K31/15 , A61K31/275 , C07C20060101 , C07C47/38 , C07C67/00 , C07C253/00 , C07C255/34 , C07C255/35 , C07C255/53 , C07C
Abstract: 1489118 Derivatives of 1,2-diphenylethylene HOECHST AG 7 March 1975 [9 March 1974 22 Feb 1975] 9585/75 Heading C2C [Also in Division A5] The invention comprises compounds of formula wherein X is CN or CH = NOH, Hal is Cl or Br, and Ar and Ar 1 are each Ph possibly substituted by 1 or 2 of halogen atoms or C 1-6 alkyl or alkoxy groups, excepting the compounds where In examples, the oximes are prepared by reacting the corresponding aldehydes with NH 2 OH, and the nitriles by dehydrating the oximes. The excepted compounds are also prepared by these methods.
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公开(公告)号:ZA7309328B
公开(公告)日:1974-10-30
申请号:ZA7309328
申请日:1973-12-07
Applicant: HOECHST AG
IPC: C07D233/60 , C07D235/06 , C07D521/00 , C07D49/36
CPC classification number: C07D235/06 , C07D231/12 , C07D233/56 , C07D249/08
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公开(公告)号:ZA735640B
公开(公告)日:1974-07-31
申请号:ZA735640
申请日:1973-08-17
Applicant: HOECHST AG
IPC: C07C69/732 , A61K31/19 , A61K31/235 , A61K31/535 , C07C51/00 , C07C51/08 , C07C59/52 , C07C67/00 , C07C69/66 , C07D295/16 , C07C
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公开(公告)号:ZA7906651B
公开(公告)日:1981-05-27
申请号:ZA7906651
申请日:1979-12-07
Applicant: HOECHST AG
IPC: A61K31/415 , A61K31/505 , A61P3/04 , A61P3/06 , C07D239/48 , C07D403/04 , C07D403/12 , C07D405/12 , C07D405/14 , C07D
CPC classification number: C07D239/48 , C07C255/00 , Y10S514/909
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公开(公告)号:DK286580A
公开(公告)日:1981-01-04
申请号:DK286580
申请日:1980-07-02
Applicant: HOECHST AG
IPC: A61K31/425 , A61K31/426 , A61P3/06 , A61P9/10 , C07C275/66 , C07C335/36 , C07D277/18 , C07D277/20 , C07D277/42 , C07D317/66 , C07D319/18 , C07D417/12 , C07D
Abstract: Thiazoline derivatives of the general formula I (I) wherein R1 to R7 have the specified meanings, physiologically acceptable acid addition salts thereof, processes for their preparation, pharmaceutical preparations based on these compounds and their use for acting on the serum lipoprotein spectrum. The invention moreover relates to compounds of the formulae (IV) (XI) (XVII) wherein A, R, R1 to R7, Y and Z have the specified meanings.
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公开(公告)号:ZA775333B
公开(公告)日:1978-07-26
申请号:ZA775333
申请日:1977-09-02
Applicant: HOECHST AG
IPC: A61K31/195 , A61K31/38 , A61K31/381 , A61P3/06 , C07C229/38 , C07C233/81 , C07C235/52 , C07D333/38 , C07C , A61K
Abstract: Benzoic acids of the general formula I I in which R, R1, R2 and Y have the meanings as mentioned in the following, and which in the form of the free compounds or in the form of the physiologically tolerated salts and esters possess valuable pharmacological properties, processes for preparing them, pharmaceutical preparations containing them, and their use as or in medicaments.
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公开(公告)号:SE7714684A
公开(公告)日:1978-06-25
申请号:SE7714684
申请日:1977-12-22
Applicant: HOECHST AG
Inventor: GEBERT U , GRANZER E , GREVE H-G , THORWART W
IPC: C07D295/08 , A61K31/445 , A61K31/451 , A61K31/495 , A61P3/06 , A61P9/00 , A61P9/10 , A61P9/12 , A61P19/06 , C07D209/14 , C07D211/14 , C07D213/53 , C07D213/80 , C07D295/088 , C07D303/12 , C07D303/36 , C07D333/22 , C07D409/12 , C07D295/12
CPC classification number: C07D213/53 , C07D209/14 , C07D211/14 , C07D213/80 , C07D295/088 , C07D303/12 , C07D333/22
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公开(公告)号:DK397777A
公开(公告)日:1978-03-09
申请号:DK397777
申请日:1977-09-07
Applicant: HOECHST AG
IPC: A61K31/425 , A61K31/428 , A61P3/06 , C07C45/63 , C07C205/45 , C07D277/60 , C07D277/84 , C07D513/04 , C07D
Abstract: Thiazolidine derivatives of the formula I I in which the substituents R1 to R7 have the meanings as indicated in the following and which have in the free form or in the form of their non toxic acid addition salts valuable pharmaceutical properties, processes for preparing them, pharmaceutical preparations on the basis of these compounds and their use as medicines.
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