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公开(公告)号:DK248476A
公开(公告)日:1976-12-06
申请号:DK248476
申请日:1976-06-04
Applicant: HOECHST AG
IPC: A61K31/275 , A61K31/357 , A61K31/36 , A61K31/42 , A61P25/04 , A61P29/00 , C07C67/00 , C07C233/00 , C07C253/00 , C07C255/30 , C07C255/58 , C07C313/00 , C07C323/41 , C07D261/18 , C07D317/58 , C07D317/66 , G05D16/06 , G05D23/12 , G09F7/00 , H01F7/02 , H01J3/02 , H01J23/00 , H01J23/065 , H01J23/087 , H01J23/42 , H01J25/38 , H01J29/38 , C07C
Abstract: Cyanoacetanilides of formula (I) are new: (where in formula (I) R1,R2 and R3 are each independently 1-3C alkyl, alkoxy or alkylthio (partly or completely substd. by some or different halo), halo, NO2, CN, 1-3C alkoxycarbonyl; also R1 and R2 can be H in which case R3 is not CH3 but may additionally be phenyl or phenoxy both opt. substd. by 1 or 2 F, Cl, Br, I or 1-3C alkyl or alkoxy; or R1 is H and R2 and R3 are methylenedioxy or complete a naphthalene ring; M is H, alkali metal or NH4). They are prepd. from the corresp. acetanilides by: (i) reacting with orthoformates; (ii) cyclising with NH2OH; then (iii) treating the isoxazole formed with base. Cpds. (I) are antiphlogistics and analgesics more powerful than phenylbutazone and without ulcerogenic effects at therapeutic doses.
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公开(公告)号:DE2046848C3
公开(公告)日:1975-06-19
申请号:DE2046848
申请日:1970-09-23
Applicant: HOECHST AG
Inventor: WOLF E , KOHL H , HERTFELDER G
IPC: C07F9/53 , C07F9/645 , C07F9/65 , A61K31/675
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公开(公告)号:BG19171A3
公开(公告)日:1975-04-30
申请号:BG1745971
申请日:1971-05-04
Applicant: HOECHST AG
Inventor: WOLF E , KOHL H , HERTFELDER G
Abstract: 1345443 Phosphorus-containing benzodiazepine derivatives FARBWERKE HOECHST AG 5 May 1971 [8 May 1970 23 Sept 1970] 13207/71 Heading C2P [Also in Division A5] The invention comprises a phosphorus-containing benzodiazepine derivative of the general formula wherein R 1 is H, NO 2 , a halogen atom, or CF 3 , R 2 is a straight or branched chain alkyl group having up to 8 carbon atoms, a hydrogen atom, a halogen atom, NO 2 or CF 3 , R 3 is a straight chain or branched chain alkyl group having up to 3 carbon atoms and n is an integer from 1 to 6: They may be obtained by (a) reacting a metal derivative of the formula wherein M is a metal cation with a phosphine oxide of the formula X(CH 2 ) n P(O)(R 3 ) 2 , wherein X is a halogen atom or an alkyl (or aryl-) sulphonyloxy group, or (b) by reacting a compound of the formula with a derivative of amino acetic acid (preferably an ester, e.g. an imino or ortho ester derivative) or (c) by reacting a compound of the above Formula IV with a halide or azide of a halogenoacetic acid, treating the product with ammonia and then cyclizing the compound so obtained. In reaction (a) the metal compound can first be formed by heating the appropriate 1-unsubstituted benzodiazepine with, e.g., Ca-, Na- or Li-hydride or with potassium tertbutylate or sodium methylate in an inert organic solvent and the product may then be formed directly by reaction with the compound X(CH 2 ) n P(O)(R 3 ) 2 in the same solvent without isolation of the metal derivative. The products are useful as tranquillizers.
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公开(公告)号:CH552632A
公开(公告)日:1974-08-15
申请号:CH664171
申请日:1971-05-05
Applicant: HOECHST AG
Inventor: WOLF E , KOHL H , HERTFELDER G
Abstract: 1345443 Phosphorus-containing benzodiazepine derivatives FARBWERKE HOECHST AG 5 May 1971 [8 May 1970 23 Sept 1970] 13207/71 Heading C2P [Also in Division A5] The invention comprises a phosphorus-containing benzodiazepine derivative of the general formula wherein R 1 is H, NO 2 , a halogen atom, or CF 3 , R 2 is a straight or branched chain alkyl group having up to 8 carbon atoms, a hydrogen atom, a halogen atom, NO 2 or CF 3 , R 3 is a straight chain or branched chain alkyl group having up to 3 carbon atoms and n is an integer from 1 to 6: They may be obtained by (a) reacting a metal derivative of the formula wherein M is a metal cation with a phosphine oxide of the formula X(CH 2 ) n P(O)(R 3 ) 2 , wherein X is a halogen atom or an alkyl (or aryl-) sulphonyloxy group, or (b) by reacting a compound of the formula with a derivative of amino acetic acid (preferably an ester, e.g. an imino or ortho ester derivative) or (c) by reacting a compound of the above Formula IV with a halide or azide of a halogenoacetic acid, treating the product with ammonia and then cyclizing the compound so obtained. In reaction (a) the metal compound can first be formed by heating the appropriate 1-unsubstituted benzodiazepine with, e.g., Ca-, Na- or Li-hydride or with potassium tertbutylate or sodium methylate in an inert organic solvent and the product may then be formed directly by reaction with the compound X(CH 2 ) n P(O)(R 3 ) 2 in the same solvent without isolation of the metal derivative. The products are useful as tranquillizers.
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公开(公告)号:DE2046848B2
公开(公告)日:1974-06-27
申请号:DE2046848
申请日:1970-09-23
Applicant: HOECHST AG
Inventor: WOLF E , KOHL H , HERTFELDER G
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公开(公告)号:DK140010C
公开(公告)日:1979-11-05
申请号:DK397670
申请日:1970-07-31
Applicant: HOECHST AG
IPC: A61K38/00 , C07D253/08 , C07K1/10 , C07K5/068 , C07K14/695
Abstract: 1318963 1,2,3 - Benzo triazines FARBWERKE HOECHST AG 3 Aug 1970 [1 Aug 1969] 37320/70 Heading C2C A 3 - hydroxy - 4 - oxo - 3,4 - dihydro - 1,2,3- benzo triazine ester of a protected amino acid or a protected peptide, which is prepared from the free 3-hydroxy benzo triazine and a protected amino acid or peptide containing a free carboxyl group in the presence of a carbo diimide, is used in the preparation of peptides wherein a carboxylic ester of a protected amino acid or peptide is reacted with an amino acid or peptide having a free amino group and protecting groups are subsequently removed. The following starting materials are prepared. Z - Asn(Mbh)OH, Z - Gln(Mbh)OH and its methyl ester and H Gln(Mbh)OMe, HCl, Z-Gly- NH-MbH, and BOC-Leu-Phe-OH, where "Mbh" is 4,4 1 -dimethoxy benzhydryl.
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公开(公告)号:DK137861B
公开(公告)日:1978-05-22
申请号:DK220771
申请日:1971-05-06
Applicant: HOECHST AG
Inventor: WOLF E , KOHL H , HAERTFELDER G
IPC: C07F9/53 , C07F9/645 , C07F9/65 , C07D243/26
Abstract: 1345443 Phosphorus-containing benzodiazepine derivatives FARBWERKE HOECHST AG 5 May 1971 [8 May 1970 23 Sept 1970] 13207/71 Heading C2P [Also in Division A5] The invention comprises a phosphorus-containing benzodiazepine derivative of the general formula wherein R 1 is H, NO 2 , a halogen atom, or CF 3 , R 2 is a straight or branched chain alkyl group having up to 8 carbon atoms, a hydrogen atom, a halogen atom, NO 2 or CF 3 , R 3 is a straight chain or branched chain alkyl group having up to 3 carbon atoms and n is an integer from 1 to 6: They may be obtained by (a) reacting a metal derivative of the formula wherein M is a metal cation with a phosphine oxide of the formula X(CH 2 ) n P(O)(R 3 ) 2 , wherein X is a halogen atom or an alkyl (or aryl-) sulphonyloxy group, or (b) by reacting a compound of the formula with a derivative of amino acetic acid (preferably an ester, e.g. an imino or ortho ester derivative) or (c) by reacting a compound of the above Formula IV with a halide or azide of a halogenoacetic acid, treating the product with ammonia and then cyclizing the compound so obtained. In reaction (a) the metal compound can first be formed by heating the appropriate 1-unsubstituted benzodiazepine with, e.g., Ca-, Na- or Li-hydride or with potassium tertbutylate or sodium methylate in an inert organic solvent and the product may then be formed directly by reaction with the compound X(CH 2 ) n P(O)(R 3 ) 2 in the same solvent without isolation of the metal derivative. The products are useful as tranquillizers.
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公开(公告)号:DE2022503C3
公开(公告)日:1974-11-28
申请号:DE2022503
申请日:1970-05-08
Applicant: HOECHST AG
Inventor: WOLF E , KOHL H , HERTFELDER G
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公开(公告)号:NO130399B
公开(公告)日:1974-08-26
申请号:NO172771
申请日:1971-05-07
Applicant: HOECHST AG
Inventor: WOLF E , KOHL H , HAERTFELDER G
Abstract: 1345443 Phosphorus-containing benzodiazepine derivatives FARBWERKE HOECHST AG 5 May 1971 [8 May 1970 23 Sept 1970] 13207/71 Heading C2P [Also in Division A5] The invention comprises a phosphorus-containing benzodiazepine derivative of the general formula wherein R 1 is H, NO 2 , a halogen atom, or CF 3 , R 2 is a straight or branched chain alkyl group having up to 8 carbon atoms, a hydrogen atom, a halogen atom, NO 2 or CF 3 , R 3 is a straight chain or branched chain alkyl group having up to 3 carbon atoms and n is an integer from 1 to 6: They may be obtained by (a) reacting a metal derivative of the formula wherein M is a metal cation with a phosphine oxide of the formula X(CH 2 ) n P(O)(R 3 ) 2 , wherein X is a halogen atom or an alkyl (or aryl-) sulphonyloxy group, or (b) by reacting a compound of the formula with a derivative of amino acetic acid (preferably an ester, e.g. an imino or ortho ester derivative) or (c) by reacting a compound of the above Formula IV with a halide or azide of a halogenoacetic acid, treating the product with ammonia and then cyclizing the compound so obtained. In reaction (a) the metal compound can first be formed by heating the appropriate 1-unsubstituted benzodiazepine with, e.g., Ca-, Na- or Li-hydride or with potassium tertbutylate or sodium methylate in an inert organic solvent and the product may then be formed directly by reaction with the compound X(CH 2 ) n P(O)(R 3 ) 2 in the same solvent without isolation of the metal derivative. The products are useful as tranquillizers.
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公开(公告)号:CH552019A
公开(公告)日:1974-07-31
申请号:CH630974
申请日:1971-05-05
Applicant: HOECHST AG
Inventor: WOLF E , KOHL H , HERTFELDER G
Abstract: 1345443 Phosphorus-containing benzodiazepine derivatives FARBWERKE HOECHST AG 5 May 1971 [8 May 1970 23 Sept 1970] 13207/71 Heading C2P [Also in Division A5] The invention comprises a phosphorus-containing benzodiazepine derivative of the general formula wherein R 1 is H, NO 2 , a halogen atom, or CF 3 , R 2 is a straight or branched chain alkyl group having up to 8 carbon atoms, a hydrogen atom, a halogen atom, NO 2 or CF 3 , R 3 is a straight chain or branched chain alkyl group having up to 3 carbon atoms and n is an integer from 1 to 6: They may be obtained by (a) reacting a metal derivative of the formula wherein M is a metal cation with a phosphine oxide of the formula X(CH 2 ) n P(O)(R 3 ) 2 , wherein X is a halogen atom or an alkyl (or aryl-) sulphonyloxy group, or (b) by reacting a compound of the formula with a derivative of amino acetic acid (preferably an ester, e.g. an imino or ortho ester derivative) or (c) by reacting a compound of the above Formula IV with a halide or azide of a halogenoacetic acid, treating the product with ammonia and then cyclizing the compound so obtained. In reaction (a) the metal compound can first be formed by heating the appropriate 1-unsubstituted benzodiazepine with, e.g., Ca-, Na- or Li-hydride or with potassium tertbutylate or sodium methylate in an inert organic solvent and the product may then be formed directly by reaction with the compound X(CH 2 ) n P(O)(R 3 ) 2 in the same solvent without isolation of the metal derivative. The products are useful as tranquillizers.
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