ES268192A1 - Procedimiento para la obtencion de derivados de hidracina - Google Patents
Procedimiento para la obtencion de derivados de hidracinaInfo
- Publication number
- ES268192A1 ES268192A1 ES0268192A ES268192A ES268192A1 ES 268192 A1 ES268192 A1 ES 268192A1 ES 0268192 A ES0268192 A ES 0268192A ES 268192 A ES268192 A ES 268192A ES 268192 A1 ES268192 A1 ES 268192A1
- Authority
- ES
- Spain
- Prior art keywords
- sulphamoyl
- chloro
- chloride
- fluorobenzoic acid
- sulphamoylphenyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 150000003456 sulfonamides Chemical class 0.000 title 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- -1 sulphamoylphenyl Chemical group 0.000 abstract 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 2
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 abstract 1
- PWVVLOWYPRNCKW-UHFFFAOYSA-N 2-chloro-5-hydrazinylbenzenesulfonamide Chemical compound NNC1=CC=C(Cl)C(S(N)(=O)=O)=C1 PWVVLOWYPRNCKW-UHFFFAOYSA-N 0.000 abstract 1
- ZAJALNCZCSSGJC-UHFFFAOYSA-N 2-chloro-5-nitrobenzenesulfonamide Chemical compound NS(=O)(=O)C1=CC([N+]([O-])=O)=CC=C1Cl ZAJALNCZCSSGJC-UHFFFAOYSA-N 0.000 abstract 1
- NSTREUWFTAOOKS-UHFFFAOYSA-N 2-fluorobenzoic acid Chemical compound OC(=O)C1=CC=CC=C1F NSTREUWFTAOOKS-UHFFFAOYSA-N 0.000 abstract 1
- LZGZJLJZSAGDKR-UHFFFAOYSA-N 3-chlorosulfonyl-4-fluorobenzoic acid Chemical compound OC(=O)C1=CC=C(F)C(S(Cl)(=O)=O)=C1 LZGZJLJZSAGDKR-UHFFFAOYSA-N 0.000 abstract 1
- NGBMRUQCUCRKQN-UHFFFAOYSA-N 4-fluoro-3-sulfamoylbenzoic acid Chemical compound NS(=O)(=O)C1=CC(C(O)=O)=CC=C1F NGBMRUQCUCRKQN-UHFFFAOYSA-N 0.000 abstract 1
- GRPUONDAGGQGJY-UHFFFAOYSA-N 4-fluoro-3-sulfamoylbenzoyl chloride Chemical compound NS(=O)(=O)C1=CC(C(Cl)=O)=CC=C1F GRPUONDAGGQGJY-UHFFFAOYSA-N 0.000 abstract 1
- FDDSVQLOFIBCDH-UHFFFAOYSA-N 5-amino-2-chlorobenzenesulfonamide Chemical compound NC1=CC=C(Cl)C(S(N)(=O)=O)=C1 FDDSVQLOFIBCDH-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 abstract 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 125000000068 chlorophenyl group Chemical group 0.000 abstract 1
- 239000002934 diuretic Substances 0.000 abstract 1
- 230000001882 diuretic effect Effects 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 125000006501 nitrophenyl group Chemical group 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 230000000894 saliuretic effect Effects 0.000 abstract 1
- 239000004289 sodium hydrogen sulphite Substances 0.000 abstract 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 abstract 1
- 239000001119 stannous chloride Substances 0.000 abstract 1
- 235000011150 stannous chloride Nutrition 0.000 abstract 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003944 tolyl group Chemical group 0.000 abstract 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH679960A CH383399A (de) | 1960-06-15 | 1960-06-15 | Verfahren zur Herstellung von neuen Hydrazinen |
| CH1002460 | 1960-09-05 | ||
| CH311761 | 1961-03-15 | ||
| CH488961 | 1961-04-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES268192A1 true ES268192A1 (es) | 1961-12-16 |
Family
ID=27428563
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0268192A Expired ES268192A1 (es) | 1960-06-15 | 1961-06-13 | Procedimiento para la obtencion de derivados de hidracina |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE604937A (fr) |
| ES (1) | ES268192A1 (fr) |
| GB (1) | GB979386A (fr) |
-
1961
- 1961-05-26 GB GB1913061A patent/GB979386A/en not_active Expired
- 1961-06-13 ES ES0268192A patent/ES268192A1/es not_active Expired
- 1961-06-13 BE BE604937A patent/BE604937A/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BE604937A (fr) | 1961-12-13 |
| GB979386A (en) | 1965-01-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES408565A1 (es) | Procedimiento para la preparacion de diaminas ciclicas di- sustituidas en n, n. | |
| GB1219035A (en) | Improvements in hair dyes | |
| GB1327312A (en) | Hererocyclic compounds | |
| GB1155937A (en) | Novel Oxazolidinones | |
| GB1344642A (en) | Meta-anilide urea compositions and their utility as herbicides | |
| GB1424773A (en) | Thiazolinyl and thiazinyl derivatives of 2-aminobenzimidazoles | |
| ES376288A1 (es) | Procedimiento para la obtencion de un medio herbicida a ba-se de esteres de acidos amidotionofosforicos. | |
| GB1338985A (en) | N-acyl-biscarbamates and herbicidal preparations containing them | |
| ES447547A1 (es) | Procedimiento para la obtencion de derivados de triazoliso- quinolina. | |
| ES268192A1 (es) | Procedimiento para la obtencion de derivados de hidracina | |
| GB1479859A (en) | Oxacyclohexane derivatives | |
| GB881616A (en) | Improvements in the production of 1-aryl-4, 5-dihalogen-pyridazones-(6) | |
| GB1054708A (fr) | ||
| GB1506022A (en) | 1-acyl-4-(o-halophenyl)thiosemicarbazides | |
| ES483676A1 (es) | Un procedimiento para preparar compuestos de acido 3-cefem- 4-carboxilico disustituidos en las posiciones 3 y 7 | |
| GB1473889A (en) | Substituted phenylureas their preparationand their herbicidal compositions | |
| GB1251147A (fr) | ||
| GB1298311A (en) | 5-imino-1,2,4,-triazine derivatives and their use as herbicides | |
| GB1330667A (en) | N-o-fluorophenylureas their manufacture and their use | |
| GB1339244A (en) | N-1,1 substituted acetonitrilo-a-3,5-substituted phenoxy alkyl amides and their use as herbicides | |
| GB1348856A (en) | Insecticidal phosphoroamidothioates and compositions containing them | |
| GB1332102A (en) | N-2-phenylisopropyl urea compounds and their use as herbicides | |
| GB947001A (en) | Substituted phenoxyalklylguanidines | |
| GB997475A (en) | Improvements in or relating to sulphonamides | |
| GB1515129A (en) | Paraphenylenediamine compounds and their use for photographic purposes |