公开(公告)号：FR2052943A1

公开(公告)日：1971-04-16

申请号：FR7021096

申请日：1970-06-09

Applicant: HOECHST AG

Inventor： RUSCHIG H ,  DUWEL D ,  KONIG J

IPC: A61K31/165 ,  A23K1/16 ,  A61K31/22 ,  A61K31/245 ,  A61P33/00 ,  C07C67/00 ,  C07C231/00 ,  C07C231/12 ,  C07C235/56 ,  C07C235/64 ,  C07D307/68 ,  F23Q7/02 ,  F24C5/14 ,  A61K27/00 ,  C07C103/00

Abstract: 1280407 Diacyloxy-benzoic acid anilides FARBWERKE HOECHST AG 9 June 1970 [9 June 1969] 27829/70 Heading C2C Novel compounds of Formula I (in which X is H or halogen; R 1 is 1 to 3 substituents selected from NO 2 , CF 3 and halogen; and R 2 is H; C 1-6 alkyl which may be substituted by one or more halogen atoms or a C 1-6 alkoxy or phenyl group; C 2-5 alkenyl; C 4-6 cycloalkyl; phenyl; an unsaturated 5- or 6- membered heterocyclic ring; C 1-4 alkylamino; di - (C 1-4 alkyl)amino ; pyrrolidino; piperidino ; morpholino; or 4-methylpiperazino) are prepared by acylating compounds of Formula II 5 - Iodo - 3 - nitro - 2,6 - dihydroxy - benzoic acid 4 1 -chloroanilide is prepared by reacting 3- nitro - 2,6 - dihydroxy - benzoic acid 4 1 - chloroanilide with iodine monochloride. Anthelmintic compositions for oral or parenteral administration, comprise a compound of Formula I together with a pharmaceutical carrier.

公开(公告)号：NL7008304A

公开(公告)日：1970-12-11

申请号：NL7008304

申请日：1970-06-08

Applicant: HOECHST AG

Inventor： RUSCHIG H ,  DUWEL D ,  KONIG J

IPC: A23K1/16 ,  A61K31/22 ,  A61K31/245 ,  A61P33/00 ,  C07C67/00 ,  A61K31/165 ,  C07C231/00 ,  C07C231/12 ,  C07C235/56 ,  C07C235/64 ,  C07D307/68 ,  F23Q7/02 ,  F24C5/14 ,  C07C103/76 ,  C07C125/06 ,  C07D5/16 ,  C07D29/24 ,  A61K27/00

Abstract: 1280407 Diacyloxy-benzoic acid anilides FARBWERKE HOECHST AG 9 June 1970 [9 June 1969] 27829/70 Heading C2C Novel compounds of Formula I (in which X is H or halogen; R 1 is 1 to 3 substituents selected from NO 2 , CF 3 and halogen; and R 2 is H; C 1-6 alkyl which may be substituted by one or more halogen atoms or a C 1-6 alkoxy or phenyl group; C 2-5 alkenyl; C 4-6 cycloalkyl; phenyl; an unsaturated 5- or 6- membered heterocyclic ring; C 1-4 alkylamino; di - (C 1-4 alkyl)amino ; pyrrolidino; piperidino ; morpholino; or 4-methylpiperazino) are prepared by acylating compounds of Formula II 5 - Iodo - 3 - nitro - 2,6 - dihydroxy - benzoic acid 4 1 -chloroanilide is prepared by reacting 3- nitro - 2,6 - dihydroxy - benzoic acid 4 1 - chloroanilide with iodine monochloride. Anthelmintic compositions for oral or parenteral administration, comprise a compound of Formula I together with a pharmaceutical carrier.

公开(公告)号：DK133148C

公开(公告)日：1976-08-30

申请号：DK295870

申请日：1970-06-08

Applicant: HOECHST AG

Inventor： RUSCHIG H ,  DYWEL D ,  KONIG J

IPC: A61K31/165 ,  A23K1/16 ,  A61K31/22 ,  A61K31/245 ,  A61P33/00 ,  C07C67/00 ,  C07C231/00 ,  C07C231/12 ,  C07C235/56 ,  C07C235/64 ,  C07D307/68 ,  F23Q7/02 ,  F24C5/14 ,  C07C103/76 ,  C07D295/14

Abstract: 1280407 Diacyloxy-benzoic acid anilides FARBWERKE HOECHST AG 9 June 1970 [9 June 1969] 27829/70 Heading C2C Novel compounds of Formula I (in which X is H or halogen; R 1 is 1 to 3 substituents selected from NO 2 , CF 3 and halogen; and R 2 is H; C 1-6 alkyl which may be substituted by one or more halogen atoms or a C 1-6 alkoxy or phenyl group; C 2-5 alkenyl; C 4-6 cycloalkyl; phenyl; an unsaturated 5- or 6- membered heterocyclic ring; C 1-4 alkylamino; di - (C 1-4 alkyl)amino ; pyrrolidino; piperidino ; morpholino; or 4-methylpiperazino) are prepared by acylating compounds of Formula II 5 - Iodo - 3 - nitro - 2,6 - dihydroxy - benzoic acid 4 1 -chloroanilide is prepared by reacting 3- nitro - 2,6 - dihydroxy - benzoic acid 4 1 - chloroanilide with iodine monochloride. Anthelmintic compositions for oral or parenteral administration, comprise a compound of Formula I together with a pharmaceutical carrier.

公开(公告)号：CA959839A

公开(公告)日：1974-12-24

申请号：CA84963

申请日：1970-06-08

Applicant: HOECHST AG

Inventor： RUSCHIG H ,  DUWEL D ,  KONIG J

IPC: A61K31/165 ,  A23K1/16 ,  A61K31/22 ,  A61K31/245 ,  A61P33/00 ,  C07C67/00 ,  C07C231/00 ,  C07C231/12 ,  C07C235/56 ,  C07C235/64 ,  C07D307/68 ,  F23Q7/02 ,  F24C5/14

Abstract: 1280407 Diacyloxy-benzoic acid anilides FARBWERKE HOECHST AG 9 June 1970 [9 June 1969] 27829/70 Heading C2C Novel compounds of Formula I (in which X is H or halogen; R 1 is 1 to 3 substituents selected from NO 2 , CF 3 and halogen; and R 2 is H; C 1-6 alkyl which may be substituted by one or more halogen atoms or a C 1-6 alkoxy or phenyl group; C 2-5 alkenyl; C 4-6 cycloalkyl; phenyl; an unsaturated 5- or 6- membered heterocyclic ring; C 1-4 alkylamino; di - (C 1-4 alkyl)amino ; pyrrolidino; piperidino ; morpholino; or 4-methylpiperazino) are prepared by acylating compounds of Formula II 5 - Iodo - 3 - nitro - 2,6 - dihydroxy - benzoic acid 4 1 -chloroanilide is prepared by reacting 3- nitro - 2,6 - dihydroxy - benzoic acid 4 1 - chloroanilide with iodine monochloride. Anthelmintic compositions for oral or parenteral administration, comprise a compound of Formula I together with a pharmaceutical carrier.

公开(公告)号：AR192556A1

公开(公告)日：1973-02-28

申请号：AR22920370

申请日：1970-06-09

Applicant: HOECHST AG

Inventor： RUSCHIG H ,  DUWEL D ,  KONIG J

IPC: A61K31/165 ,  A23K1/16 ,  A61K31/22 ,  A61K31/245 ,  A61P33/00 ,  C07C67/00 ,  C07C231/00 ,  C07C231/12 ,  C07C235/56 ,  C07C235/64 ,  C07D307/68 ,  F23Q7/02 ,  F24C5/14

Abstract: 1280407 Diacyloxy-benzoic acid anilides FARBWERKE HOECHST AG 9 June 1970 [9 June 1969] 27829/70 Heading C2C Novel compounds of Formula I (in which X is H or halogen; R 1 is 1 to 3 substituents selected from NO 2 , CF 3 and halogen; and R 2 is H; C 1-6 alkyl which may be substituted by one or more halogen atoms or a C 1-6 alkoxy or phenyl group; C 2-5 alkenyl; C 4-6 cycloalkyl; phenyl; an unsaturated 5- or 6- membered heterocyclic ring; C 1-4 alkylamino; di - (C 1-4 alkyl)amino ; pyrrolidino; piperidino ; morpholino; or 4-methylpiperazino) are prepared by acylating compounds of Formula II 5 - Iodo - 3 - nitro - 2,6 - dihydroxy - benzoic acid 4 1 -chloroanilide is prepared by reacting 3- nitro - 2,6 - dihydroxy - benzoic acid 4 1 - chloroanilide with iodine monochloride. Anthelmintic compositions for oral or parenteral administration, comprise a compound of Formula I together with a pharmaceutical carrier.

公开(公告)号：DE1929150A1

公开(公告)日：1970-12-23

申请号：DE1929150

申请日：1969-06-09

Applicant: HOECHST AG

Inventor： RUSCHIG H ,  DUWEL D ,  KONIG J

IPC: A61K31/165 ,  A23K1/16 ,  A61K31/22 ,  A61K31/245 ,  A61P33/00 ,  C07C67/00 ,  C07C231/00 ,  C07C231/12 ,  C07C235/56 ,  C07C235/64 ,  C07D307/68 ,  F23Q7/02 ,  F24C5/14 ,  C07C103/76

Abstract: 1280407 Diacyloxy-benzoic acid anilides FARBWERKE HOECHST AG 9 June 1970 [9 June 1969] 27829/70 Heading C2C Novel compounds of Formula I (in which X is H or halogen; R 1 is 1 to 3 substituents selected from NO 2 , CF 3 and halogen; and R 2 is H; C 1-6 alkyl which may be substituted by one or more halogen atoms or a C 1-6 alkoxy or phenyl group; C 2-5 alkenyl; C 4-6 cycloalkyl; phenyl; an unsaturated 5- or 6- membered heterocyclic ring; C 1-4 alkylamino; di - (C 1-4 alkyl)amino ; pyrrolidino; piperidino ; morpholino; or 4-methylpiperazino) are prepared by acylating compounds of Formula II 5 - Iodo - 3 - nitro - 2,6 - dihydroxy - benzoic acid 4 1 -chloroanilide is prepared by reacting 3- nitro - 2,6 - dihydroxy - benzoic acid 4 1 - chloroanilide with iodine monochloride. Anthelmintic compositions for oral or parenteral administration, comprise a compound of Formula I together with a pharmaceutical carrier.

公开(公告)号：BE751690A

公开(公告)日：1970-12-09

申请号：BE751690D

申请日：1970-06-09

Applicant: HOECHST AG

Inventor： RUSCHIG H ,  DUWEL D ,  KONIG J

IPC: A61K31/165 ,  A23K1/16 ,  A61K31/22 ,  A61K31/245 ,  A61P33/00 ,  C07C67/00 ,  C07C231/00 ,  C07C231/12 ,  C07C235/56 ,  C07C235/64 ,  C07D307/68 ,  F23Q7/02 ,  F24C5/14 ,  C07C

Abstract: 1280407 Diacyloxy-benzoic acid anilides FARBWERKE HOECHST AG 9 June 1970 [9 June 1969] 27829/70 Heading C2C Novel compounds of Formula I (in which X is H or halogen; R 1 is 1 to 3 substituents selected from NO 2 , CF 3 and halogen; and R 2 is H; C 1-6 alkyl which may be substituted by one or more halogen atoms or a C 1-6 alkoxy or phenyl group; C 2-5 alkenyl; C 4-6 cycloalkyl; phenyl; an unsaturated 5- or 6- membered heterocyclic ring; C 1-4 alkylamino; di - (C 1-4 alkyl)amino ; pyrrolidino; piperidino ; morpholino; or 4-methylpiperazino) are prepared by acylating compounds of Formula II 5 - Iodo - 3 - nitro - 2,6 - dihydroxy - benzoic acid 4 1 -chloroanilide is prepared by reacting 3- nitro - 2,6 - dihydroxy - benzoic acid 4 1 - chloroanilide with iodine monochloride. Anthelmintic compositions for oral or parenteral administration, comprise a compound of Formula I together with a pharmaceutical carrier.