SU272184A1 - - Google Patents
Info
- Publication number
- SU272184A1 SU272184A1 SU1159184A SU1159184A SU272184A1 SU 272184 A1 SU272184 A1 SU 272184A1 SU 1159184 A SU1159184 A SU 1159184A SU 1159184 A SU1159184 A SU 1159184A SU 272184 A1 SU272184 A1 SU 272184A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- ethyl
- benzenesulfo
- urea
- methoxy
- methanol
- Prior art date
Links
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 85
- 125000003545 alkoxy group Chemical group 0.000 description 24
- -1 chlorocyclohexyl Chemical group 0.000 description 18
- 239000004202 carbamide Substances 0.000 description 15
- 125000000217 alkyl group Chemical group 0.000 description 11
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 10
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 9
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical class 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 125000003884 phenylalkyl group Chemical group 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 125000005083 alkoxyalkoxy group Chemical group 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 125000005843 halogen group Chemical group 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- 125000002252 acyl group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 2
- GTCAXTIRRLKXRU-UHFFFAOYSA-N carbamic acid methyl ester Natural products COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 description 2
- 229910000428 cobalt oxide Inorganic materials 0.000 description 2
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 description 2
- 125000000000 cycloalkoxy group Chemical group 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 125000004438 haloalkoxy group Chemical group 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 125000003003 spiro group Chemical group 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- YORNKGLZYFTHGX-UHFFFAOYSA-N 3-ethoxy-4-methylcyclohexan-1-amine Chemical compound CCOC1CC(N)CCC1C YORNKGLZYFTHGX-UHFFFAOYSA-N 0.000 description 1
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 150000001555 benzenes Chemical group 0.000 description 1
- 125000005521 carbonamide group Chemical group 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 150000007524 organic acids Chemical group 0.000 description 1
- 125000002071 phenylalkoxy group Chemical group 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1966F0049329 DE1252201B (de) | 1966-05-28 | 1966-05-28 | Verfahren zur Herstellung von Benzolsulfonylharnstoffen |
| DE1967F0052152 DE1618402B2 (de) | 1966-05-28 | 1967-04-18 | Benzolsulfonylharnstoffe, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische praeparate |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SU272184A1 true SU272184A1 (enExample) | |
| SU465783A3 SU465783A3 (ru) | 1975-03-30 |
Family
ID=25977218
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1443578A SU465783A3 (ru) | 1966-05-28 | 1967-05-27 | Способ получени бензолсульфонилмочевины |
| SU1443576A SU407445A3 (enExample) | 1966-05-28 | 1967-05-27 | |
| SU1444380A SU468403A3 (ru) | 1966-05-28 | 1967-05-28 | Способ получени бензолсульфонилмочевины |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1443576A SU407445A3 (enExample) | 1966-05-28 | 1967-05-27 | |
| SU1444380A SU468403A3 (ru) | 1966-05-28 | 1967-05-28 | Способ получени бензолсульфонилмочевины |
Country Status (22)
| Country | Link |
|---|---|
| JP (1) | JPS5133903B1 (enExample) |
| AR (3) | AR192396A1 (enExample) |
| AT (2) | AT324349B (enExample) |
| BE (1) | BE699134A (enExample) |
| CH (7) | CH503709A (enExample) |
| CY (1) | CY567A (enExample) |
| DE (1) | DE1618402B2 (enExample) |
| DK (1) | DK129414B (enExample) |
| ES (2) | ES340953A1 (enExample) |
| FI (1) | FI46155C (enExample) |
| FR (2) | FR1524754A (enExample) |
| GB (1) | GB1182694A (enExample) |
| IL (1) | IL28034A (enExample) |
| IS (1) | IS734B6 (enExample) |
| LU (1) | LU53740A1 (enExample) |
| MC (1) | MC654A1 (enExample) |
| MY (1) | MY7100059A (enExample) |
| NL (2) | NL157592B (enExample) |
| NO (1) | NO122921B (enExample) |
| OA (1) | OA03625A (enExample) |
| SE (1) | SE336331B (enExample) |
| SU (3) | SU465783A3 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL7200696A (enExample) * | 1971-01-23 | 1972-07-25 | ||
| BR112019024831A2 (pt) | 2017-05-24 | 2020-06-09 | The University Of Queensland | composto, sal, solvato ou pró-droga, composição farmacêutica, método de tratamento ou prevenção de uma doença, método para inibir o nlrp3 |
-
1967
- 1967-04-18 DE DE1967F0052152 patent/DE1618402B2/de active Granted
- 1967-05-22 DK DK266367AA patent/DK129414B/da unknown
- 1967-05-23 FI FI671459A patent/FI46155C/fi active
- 1967-05-24 LU LU53740D patent/LU53740A1/xx unknown
- 1967-05-24 IS IS1648A patent/IS734B6/is unknown
- 1967-05-24 ES ES340953A patent/ES340953A1/es not_active Expired
- 1967-05-24 IL IL28034A patent/IL28034A/en unknown
- 1967-05-25 CH CH739467A patent/CH503709A/de not_active IP Right Cessation
- 1967-05-25 CH CH1948569A patent/CH533090A/de not_active IP Right Cessation
- 1967-05-25 CH CH1948669A patent/CH502318A/de not_active IP Right Cessation
- 1967-05-25 CH CH1948769A patent/CH502319A/de not_active IP Right Cessation
- 1967-05-25 CH CH1948869A patent/CH502320A/de not_active IP Right Cessation
- 1967-05-25 CH CH979571A patent/CH533091A/de not_active IP Right Cessation
- 1967-05-25 CH CH1948469A patent/CH502998A/de not_active IP Right Cessation
- 1967-05-26 NL NL6707340.A patent/NL157592B/xx unknown
- 1967-05-26 AT AT493767A patent/AT324349B/de not_active IP Right Cessation
- 1967-05-26 AT AT375674A patent/AT326682B/de active
- 1967-05-26 SE SE07405/67A patent/SE336331B/xx unknown
- 1967-05-26 MC MC694A patent/MC654A1/fr unknown
- 1967-05-27 SU SU1443578A patent/SU465783A3/ru active
- 1967-05-27 SU SU1443576A patent/SU407445A3/ru active
- 1967-05-27 NO NO168334A patent/NO122921B/no unknown
- 1967-05-27 OA OA52951A patent/OA03625A/xx unknown
- 1967-05-28 SU SU1444380A patent/SU468403A3/ru active
- 1967-05-29 FR FR108207A patent/FR1524754A/fr not_active Expired
- 1967-05-29 JP JP42034115A patent/JPS5133903B1/ja active Pending
- 1967-05-29 BE BE699134D patent/BE699134A/xx unknown
- 1967-05-30 GB GB24852/67A patent/GB1182694A/en not_active Expired
- 1967-08-25 FR FR119022A patent/FR6497M/fr not_active Expired
-
1968
- 1968-05-11 ES ES353814A patent/ES353814A1/es not_active Expired
-
1970
- 1970-04-10 AR AR228019A patent/AR192396A1/es active
- 1970-11-26 CY CY56770A patent/CY567A/xx unknown
-
1971
- 1971-12-30 MY MY59/71A patent/MY7100059A/xx unknown
-
1972
- 1972-12-28 AR AR245895A patent/AR193007A1/es active
- 1972-12-31 AR AR245611A patent/AR192829A1/es active
-
1978
- 1978-02-10 NL NL7801563A patent/NL7801563A/xx unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH05294954A (ja) | 新規ベンゾピラン誘導体 | |
| NO340366B1 (no) | Metode for fremstilling av 3-(2-(1-benzotiofen-5-yl)etoksy)propionsyre eller salter derav | |
| NO122789B (enExample) | ||
| SU272184A1 (enExample) | ||
| US2567651A (en) | J-dialkyl-g-amino-l | |
| Angier et al. | Pteroic acid derivatives. VI. Unequivocal syntheses of some isomeric glutamic acid peptides | |
| RU2052458C1 (ru) | Способ получения производных тетразолуксусной кислоты | |
| US3969409A (en) | 3-Anilino-5,5-disubstituted-2-aminomethyl-2-cyclohexen-1-ones and the salts thereof | |
| NO120075B (enExample) | ||
| Takagi et al. | Synthesis of nitro and Amino N‐heterocycles via Ring Transformation of 2‐methyl‐3‐nitrochromone | |
| US2470108A (en) | Heterocyclic amines | |
| RU2646756C2 (ru) | Производное кумарина | |
| EP0291565A1 (en) | Preparation of 3,5-dicarboxylic esters of 2,6-bis (Fluoroalkyl) piperidines | |
| US2332906A (en) | Process for preparation of sulphonamide derivatives | |
| US4822895A (en) | 3-aminoazetidine, its salts and intermediates of synthesis | |
| US2288531A (en) | Benzenesulphonamide compounds | |
| US3994879A (en) | Process for the preparation of benzofuran compounds | |
| IE45782B1 (en) | 1-(n-acylcarbamoyl)-2-cyanoziridines | |
| US3818023A (en) | 2-phenyl benzothiazolyl acetic acid derivatives | |
| SU455533A3 (ru) | Способ получени производных 4-хлор-5-сульфамоилантраниловой кислоты | |
| US2694720A (en) | N-acylated phenolsulfonamides | |
| NO119593B (enExample) | ||
| US3733338A (en) | 1-oxo-isochromenes | |
| SU738510A3 (ru) | Способ получени 2,3-дигидробензо (в) тиофенонов-2 или их солей | |
| US3546216A (en) | Schiff bases of amino-substituted tetrahydrothiophene 1,1-dioxides |