JPH0149263B2 - - Google Patents
Info
- Publication number
- JPH0149263B2 JPH0149263B2 JP57123733A JP12373382A JPH0149263B2 JP H0149263 B2 JPH0149263 B2 JP H0149263B2 JP 57123733 A JP57123733 A JP 57123733A JP 12373382 A JP12373382 A JP 12373382A JP H0149263 B2 JPH0149263 B2 JP H0149263B2
- Authority
- JP
- Japan
- Prior art keywords
- temperature
- reaction formula
- following reaction
- isopropyl
- synthesis method
- 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
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 claims abstract description 10
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 claims abstract description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 5
- 238000001914 filtration Methods 0.000 claims abstract description 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 16
- 238000006243 chemical reaction Methods 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 9
- VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 claims description 8
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 8
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 claims description 6
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 claims description 5
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 claims description 4
- 239000012024 dehydrating agents Substances 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical compound NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 230000002194 synthesizing effect Effects 0.000 claims description 2
- 238000001308 synthesis method Methods 0.000 claims 3
- 238000007865 diluting Methods 0.000 claims 1
- 238000010790 dilution Methods 0.000 abstract description 2
- 239000012895 dilution Substances 0.000 abstract description 2
- 239000002253 acid Substances 0.000 abstract 1
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 abstract 1
- OUPVTMCNLOJJSK-UHFFFAOYSA-N methyl 2-(propan-2-ylsulfamoylamino)benzoate Chemical compound COC(=O)C1=CC=CC=C1NS(=O)(=O)NC(C)C OUPVTMCNLOJJSK-UHFFFAOYSA-N 0.000 abstract 1
- 150000004702 methyl esters Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 5
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- DXUMYHZTYVPBEZ-UHFFFAOYSA-N 2,4,6-tris(trichloromethyl)-1,3,5-triazine Chemical group ClC(Cl)(Cl)C1=NC(C(Cl)(Cl)Cl)=NC(C(Cl)(Cl)Cl)=N1 DXUMYHZTYVPBEZ-UHFFFAOYSA-N 0.000 description 1
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- WSZJADHVJOBSJL-UHFFFAOYSA-N methyl 2-(sulfamoylamino)benzoate Chemical compound COC(=O)C1=CC=CC=C1NS(N)(=O)=O WSZJADHVJOBSJL-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- AGRDPCWQGGNEQL-UHFFFAOYSA-N n-propan-2-ylsulfamoyl chloride Chemical compound CC(C)NS(Cl)(=O)=O AGRDPCWQGGNEQL-UHFFFAOYSA-N 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- QAHVHSLSRLSVGS-UHFFFAOYSA-N sulfamoyl chloride Chemical compound NS(Cl)(=O)=O QAHVHSLSRLSVGS-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C307/00—Amides of sulfuric acids, i.e. compounds having singly-bound oxygen atoms of sulfate groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C307/02—Monoamides of sulfuric acids or esters thereof, e.g. sulfamic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Indole Compounds (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT23001/81A IT1194142B (it) | 1981-07-17 | 1981-07-17 | Procedimento per eseguire la sintesi di n-isopropil-n'-o-carbometossifenils olfammide |
| IT23001A/81 | 1981-07-17 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5824556A JPS5824556A (ja) | 1983-02-14 |
| JPH0149263B2 true JPH0149263B2 (en]) | 1989-10-24 |
Family
ID=11202729
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57123733A Granted JPS5824556A (ja) | 1981-07-17 | 1982-07-15 | Ｎ−イソプロピル−ｎ′−ｏ−カルボメトキシフエニサルフアミドの合成法 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US4438276A (en]) |
| EP (1) | EP0070467B1 (en]) |
| JP (1) | JPS5824556A (en]) |
| AT (1) | ATE15657T1 (en]) |
| AU (1) | AU552767B2 (en]) |
| BR (1) | BR8204153A (en]) |
| CA (1) | CA1167861A (en]) |
| DE (1) | DE3266385D1 (en]) |
| DK (1) | DK319382A (en]) |
| ES (1) | ES8305320A1 (en]) |
| IL (1) | IL66273A (en]) |
| IT (1) | IT1194142B (en]) |
| MX (1) | MX156052A (en]) |
| SU (1) | SU1402255A3 (en]) |
| YU (1) | YU42599B (en]) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60184875A (ja) * | 1984-03-05 | 1985-09-20 | Fuji Photo Film Co Ltd | 感熱記録紙 |
| DE3428837A1 (de) * | 1984-06-30 | 1986-01-09 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von n-phenyl(pyridyl)-sulfonyldiamiden |
| JP4835632B2 (ja) * | 2008-04-22 | 2011-12-14 | トヨタ自動車株式会社 | 動力伝達装置の潤滑構造 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL197246A (en]) | 1954-05-14 |
-
1981
- 1981-07-17 IT IT23001/81A patent/IT1194142B/it active
-
1982
- 1982-06-16 MX MX193641A patent/MX156052A/es unknown
- 1982-07-08 EP EP82106121A patent/EP0070467B1/en not_active Expired
- 1982-07-08 AT AT82106121T patent/ATE15657T1/de not_active IP Right Cessation
- 1982-07-08 IL IL66273A patent/IL66273A/xx unknown
- 1982-07-08 DE DE8282106121T patent/DE3266385D1/de not_active Expired
- 1982-07-13 CA CA000407184A patent/CA1167861A/en not_active Expired
- 1982-07-13 US US06/397,878 patent/US4438276A/en not_active Expired - Fee Related
- 1982-07-14 AU AU85998/82A patent/AU552767B2/en not_active Ceased
- 1982-07-15 DK DK319382A patent/DK319382A/da not_active Application Discontinuation
- 1982-07-15 JP JP57123733A patent/JPS5824556A/ja active Granted
- 1982-07-16 BR BR8204153A patent/BR8204153A/pt not_active IP Right Cessation
- 1982-07-16 YU YU1558/82A patent/YU42599B/xx unknown
- 1982-07-16 ES ES514055A patent/ES8305320A1/es not_active Expired
-
1985
- 1985-08-16 SU SU853940049A patent/SU1402255A3/ru active
Also Published As
| Publication number | Publication date |
|---|---|
| ES514055A0 (es) | 1983-04-01 |
| AU8599882A (en) | 1983-01-20 |
| IL66273A0 (en) | 1982-11-30 |
| AU552767B2 (en) | 1986-06-19 |
| ES8305320A1 (es) | 1983-04-01 |
| IT1194142B (it) | 1988-09-14 |
| SU1402255A3 (ru) | 1988-06-07 |
| YU42599B (en) | 1988-10-31 |
| YU155882A (en) | 1984-12-31 |
| US4438276A (en) | 1984-03-20 |
| MX156052A (es) | 1988-06-22 |
| ATE15657T1 (de) | 1985-10-15 |
| IL66273A (en) | 1985-08-30 |
| CA1167861A (en) | 1984-05-22 |
| IT8123001A0 (it) | 1981-07-17 |
| BR8204153A (pt) | 1983-07-12 |
| DE3266385D1 (en) | 1985-10-24 |
| DK319382A (da) | 1983-01-18 |
| JPS5824556A (ja) | 1983-02-14 |
| EP0070467B1 (en) | 1985-09-18 |
| EP0070467A2 (en) | 1983-01-26 |
| EP0070467A3 (en) | 1984-03-21 |
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