NO122700B - - Google Patents
Download PDFInfo
- Publication number
- NO122700B NO122700B NO167411A NO16741167A NO122700B NO 122700 B NO122700 B NO 122700B NO 167411 A NO167411 A NO 167411A NO 16741167 A NO16741167 A NO 16741167A NO 122700 B NO122700 B NO 122700B
- Authority
- NO
- Norway
- Prior art keywords
- acid
- formula
- urea
- mmol
- reaction
- Prior art date
Links
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 42
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 claims description 19
- 239000003208 petroleum Substances 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 6
- -1 alkali metal salt Chemical class 0.000 claims description 6
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 150000004820 halides Chemical class 0.000 claims description 4
- VSNHCAURESNICA-UHFFFAOYSA-N Hydroxyurea Chemical class NC(=O)NO VSNHCAURESNICA-UHFFFAOYSA-N 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 150000003454 sulfinic acid halides Chemical class 0.000 claims description 3
- 229940100389 Sulfonylurea Drugs 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 229930195733 hydrocarbon Natural products 0.000 claims description 2
- 150000002430 hydrocarbons Chemical class 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 claims description 2
- 239000000725 suspension Substances 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- 238000003756 stirring Methods 0.000 description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 238000009835 boiling Methods 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
- APTFDFXACXBQDO-UHFFFAOYSA-N 1-butyl-3-hydroxyurea Chemical compound CCCCNC(=O)NO APTFDFXACXBQDO-UHFFFAOYSA-N 0.000 description 5
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 5
- 239000008346 aqueous phase Substances 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 238000001953 recrystallisation Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- JLRGJRBPOGGCBT-UHFFFAOYSA-N Tolbutamide Chemical compound CCCCNC(=O)NS(=O)(=O)C1=CC=C(C)C=C1 JLRGJRBPOGGCBT-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- JEHKKBHWRAXMCH-UHFFFAOYSA-N benzenesulfinic acid Chemical compound O[S@@](=O)C1=CC=CC=C1 JEHKKBHWRAXMCH-UHFFFAOYSA-N 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000002178 crystalline material Substances 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 229960001330 hydroxycarbamide Drugs 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 230000020477 pH reduction Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- TYZHJGCYLYXPSB-UHFFFAOYSA-N 1-(4-chlorophenyl)sulfonyl-3-cyclohexylurea Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)NC(=O)NC1CCCCC1 TYZHJGCYLYXPSB-UHFFFAOYSA-N 0.000 description 1
- XDUXYYDDHASTLI-UHFFFAOYSA-N 1-(benzenesulfonyl)-3-propylurea Chemical compound CCCNC(=O)NS(=O)(=O)C1=CC=CC=C1 XDUXYYDDHASTLI-UHFFFAOYSA-N 0.000 description 1
- YWXUADNLTYADPN-UHFFFAOYSA-N 1-butyl-3-(4-chlorophenyl)sulfonylurea Chemical compound CCCCNC(=O)NS(=O)(=O)C1=CC=C(Cl)C=C1 YWXUADNLTYADPN-UHFFFAOYSA-N 0.000 description 1
- IRMBSCHMQJLMEG-UHFFFAOYSA-N 1-butyl-3-(4-methoxyphenyl)sulfonylurea Chemical compound CCCCNC(=O)NS(=O)(=O)C1=CC=C(OC)C=C1 IRMBSCHMQJLMEG-UHFFFAOYSA-N 0.000 description 1
- AFPCHXICZQCREU-UHFFFAOYSA-N 1-hydroxy-3-propylurea Chemical compound CCCNC(=O)NO AFPCHXICZQCREU-UHFFFAOYSA-N 0.000 description 1
- DILXLMRYFWFBGR-UHFFFAOYSA-N 2-formylbenzene-1,4-disulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(S(O)(=O)=O)C(C=O)=C1 DILXLMRYFWFBGR-UHFFFAOYSA-N 0.000 description 1
- YDQNDKBOOVXRTL-UHFFFAOYSA-N 4-acetamidobenzenesulfinic acid Chemical compound CC(=O)NC1=CC=C(S(O)=O)C=C1 YDQNDKBOOVXRTL-UHFFFAOYSA-N 0.000 description 1
- AOQYAMDZQAEDLO-UHFFFAOYSA-N 4-chlorobenzenesulfinic acid Chemical compound OS(=O)C1=CC=C(Cl)C=C1 AOQYAMDZQAEDLO-UHFFFAOYSA-N 0.000 description 1
- YVZWQPOTHRMEQW-UHFFFAOYSA-N 4-methoxybenzenesulfinic acid Chemical compound COC1=CC=C(S(O)=O)C=C1 YVZWQPOTHRMEQW-UHFFFAOYSA-N 0.000 description 1
- DYYLCPSSSFWEEA-UHFFFAOYSA-N 4-methylbenzenesulfinyl chloride Chemical compound CC1=CC=C(S(Cl)=O)C=C1 DYYLCPSSSFWEEA-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
- 239000012346 acetyl chloride Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 230000003178 anti-diabetic effect Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 125000004391 aryl sulfonyl group Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- RIGBPMDIGYBTBJ-UHFFFAOYSA-N glycyclamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(=O)NC1CCCCC1 RIGBPMDIGYBTBJ-UHFFFAOYSA-N 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- AFOGBLYPWJJVAL-UHFFFAOYSA-N phenbutamide Chemical compound CCCCNC(=O)NS(=O)(=O)C1=CC=CC=C1 AFOGBLYPWJJVAL-UHFFFAOYSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- KFZUDNZQQCWGKF-UHFFFAOYSA-M sodium;4-methylbenzenesulfinate Chemical compound [Na+].CC1=CC=C(S([O-])=O)C=C1 KFZUDNZQQCWGKF-UHFFFAOYSA-M 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 150000003453 sulfinic acid esters Chemical class 0.000 description 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
- IWOKCMBOJXYDEE-UHFFFAOYSA-N sulfinylmethane Chemical compound C=S=O IWOKCMBOJXYDEE-UHFFFAOYSA-N 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical compound OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
- C07C303/40—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1375466 | 1966-03-29 | ||
| GB33463/66A GB1185013A (en) | 1966-03-29 | 1966-07-26 | Preparation of Aryl-Sulphonyl Ureas |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO122700B true NO122700B (de) | 1971-08-02 |
Family
ID=26249980
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO167411A NO122700B (de) | 1966-03-29 | 1967-03-21 |
Country Status (11)
| Country | Link |
|---|---|
| AT (1) | AT278028B (de) |
| CH (1) | CH484881A (de) |
| DE (1) | DE1618731A1 (de) |
| DK (1) | DK117346B (de) |
| ES (1) | ES338563A1 (de) |
| FI (1) | FI45754C (de) |
| GB (1) | GB1185013A (de) |
| IS (1) | IS810B6 (de) |
| NL (1) | NL6704487A (de) |
| NO (1) | NO122700B (de) |
| SE (1) | SE342615B (de) |
-
1966
- 1966-07-26 GB GB33463/66A patent/GB1185013A/en not_active Expired
-
1967
- 1967-03-15 IS IS1629A patent/IS810B6/is unknown
- 1967-03-20 CH CH395667A patent/CH484881A/de not_active IP Right Cessation
- 1967-03-21 DE DE19671618731 patent/DE1618731A1/de active Pending
- 1967-03-21 AT AT270167A patent/AT278028B/de not_active IP Right Cessation
- 1967-03-21 NO NO167411A patent/NO122700B/no unknown
- 1967-03-22 DK DK149867AA patent/DK117346B/da unknown
- 1967-03-22 FI FI670860A patent/FI45754C/fi active
- 1967-03-28 SE SE4237/67A patent/SE342615B/xx unknown
- 1967-03-28 ES ES338563A patent/ES338563A1/es not_active Expired
- 1967-03-29 NL NL6704487A patent/NL6704487A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES338563A1 (es) | 1969-10-16 |
| FI45754C (fi) | 1972-09-11 |
| SE342615B (de) | 1972-02-14 |
| DK117346B (da) | 1970-04-20 |
| GB1185013A (en) | 1970-03-18 |
| CH484881A (de) | 1970-01-31 |
| NL6704487A (de) | 1967-10-02 |
| AT278028B (de) | 1970-01-26 |
| DE1618731A1 (de) | 1971-02-18 |
| IS1629A7 (is) | 1967-09-30 |
| IS810B6 (is) | 1972-05-02 |
| FI45754B (de) | 1972-05-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2511214C (en) | Asthma and allergic inflammation modulators | |
| EP0478558B1 (de) | Verbessertes verfahren zur darstellung substituierter isoflavonderivate | |
| US2554816A (en) | Heterocyclic sulfonamides and methods of preparation thereof | |
| WO2008137027A2 (en) | Compounds as crth2 and/or pgd2 receptors modulators and their use for treating asthma and allergic inflammation | |
| WO2003076374A1 (fr) | Procede de production de derive d'acide trans-4-amino-1-cyclohexanecarboxylique | |
| US3016403A (en) | 1-aryl-3-hydroxypropyl sulfones and processes | |
| NO122700B (de) | ||
| SU508182A3 (ru) | Способ получени замещенного фенил-ацетилгуанидина | |
| SE449746B (sv) | Forfarande for framstellning av 4-metyl-5-alkyl-tioimidazoler | |
| JP3541384B2 (ja) | オキシスルホニルカルバメート | |
| US2723977A (en) | 5, 6-disubstituted 2-amino-4-pyrimidols | |
| SU609464A3 (ru) | Способ получени производных -/2-пирролидинилметил/ бензамидов или их солей | |
| US2802013A (en) | 2-(oxo and imino)-3-(phenyl and halophenyl)-tetrahydrofuransulfones and processes for the manufacture thereof | |
| US2790807A (en) | Certain carbethoxy derivatives of | |
| US3390150A (en) | Process for the preparation of 1-(beta-hydroxyethyl)-5-nitroimidazole-2-carboxylic acid gamma-lactone | |
| JPS6355512B2 (de) | ||
| JP2967231B2 (ja) | １，４―チアジン誘導体 | |
| US2535971A (en) | 1-carbalkoxy-4-substituted piperazines | |
| HU196386B (en) | Process for production of derivatives of substituated ethan-diimid-amid | |
| US2303972A (en) | Sulphanilyl guanylureas and process for making them | |
| NO133892B (de) | ||
| IL28034A (en) | Benzenesulfonyl ureas and process for their preparation | |
| IL26927A (en) | Benzenesulfonyl-ureas and process for their manufacture | |
| US2721204A (en) | Derivatives of 1, 3, 4-thiadiazole-5-sulfonamides | |
| US3152123A (en) | Process for the preparation of benzo- |