SU1405703A3 - Способ получени 2-метил-4-гидрокси-2Н-1,2-бензотиазин-1,1-диоксид-3-N-(2-пиридил)-карбоксамида - Google Patents
Способ получени 2-метил-4-гидрокси-2Н-1,2-бензотиазин-1,1-диоксид-3-N-(2-пиридил)-карбоксамида Download PDFInfo
- Publication number
- SU1405703A3 SU1405703A3 SU843805901A SU3805901A SU1405703A3 SU 1405703 A3 SU1405703 A3 SU 1405703A3 SU 843805901 A SU843805901 A SU 843805901A SU 3805901 A SU3805901 A SU 3805901A SU 1405703 A3 SU1405703 A3 SU 1405703A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- methyl
- dioxide
- benzothiazine
- carboxamide
- pyridyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 5
- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 claims description 10
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 claims description 6
- 238000007098 aminolysis reaction Methods 0.000 claims description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 claims 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims 1
- 239000012442 inert solvent Substances 0.000 claims 1
- 239000000047 product Substances 0.000 description 5
- YMWUJEATGCHHMB-UHFFFAOYSA-N dichloromethane Substances ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- QYSPLQLAKJAUJT-UHFFFAOYSA-N piroxicam Chemical compound OC=1C2=CC=CC=C2S(=O)(=O)N(C)C=1C(=O)NC1=CC=CC=N1 QYSPLQLAKJAUJT-UHFFFAOYSA-N 0.000 description 3
- 229960002702 piroxicam Drugs 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000003110 anti-inflammatory effect Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- WJGAPUXHSQQWQF-UHFFFAOYSA-N acetic acid;hydrochloride Chemical compound Cl.CC(O)=O WJGAPUXHSQQWQF-UHFFFAOYSA-N 0.000 description 1
- 230000000202 analgesic effect Effects 0.000 description 1
- 230000001760 anti-analgesic effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 1
- 229910052611 pyroxene Inorganic materials 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 235000012712 vegetable carbon Nutrition 0.000 description 1
- 239000004108 vegetable carbon Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D279/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one sulfur atom as the only ring hetero atoms
- C07D279/02—1,2-Thiazines; Hydrogenated 1,2-thiazines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FI833628A FI72317C (fi) | 1983-10-06 | 1983-10-06 | Foerfarande foer framstaellning av farmaceutiskt anvaendbar 2-metyl-4-hydroxi-2h-1,2-benzotiazin-1,1-dioxid -3-(n-2-pyridyl)-karboxamid och i foerfarandet anvaendbar mellanprodukt. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU1405703A3 true SU1405703A3 (ru) | 1988-06-23 |
Family
ID=8517867
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU843805901A SU1405703A3 (ru) | 1983-10-06 | 1984-10-05 | Способ получени 2-метил-4-гидрокси-2Н-1,2-бензотиазин-1,1-диоксид-3-N-(2-пиридил)-карбоксамида |
Country Status (16)
| Country | Link |
|---|---|
| AT (1) | AT387775B (cs) |
| BE (1) | BE900758A (cs) |
| CA (1) | CA1246066A (cs) |
| CS (1) | CS253593B2 (cs) |
| DD (1) | DD224594A5 (cs) |
| DK (1) | DK154504C (cs) |
| ES (1) | ES8505937A1 (cs) |
| FI (1) | FI72317C (cs) |
| HU (2) | HU194559B (cs) |
| IT (1) | IT1218850B (cs) |
| NO (1) | NO159275C (cs) |
| PL (1) | PL143957B1 (cs) |
| PT (1) | PT79326B (cs) |
| SE (2) | SE460789B (cs) |
| SU (1) | SU1405703A3 (cs) |
| YU (2) | YU43381B (cs) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4289879A (en) * | 1980-09-29 | 1981-09-15 | Pfizer Inc. | Synthetic method and intermediate for piroxicam |
| JPH08270888A (ja) * | 1995-03-30 | 1996-10-15 | Nec Eng Ltd | 断熱締結機構 |
-
1983
- 1983-10-06 FI FI833628A patent/FI72317C/fi not_active IP Right Cessation
-
1984
- 1984-10-01 NO NO843949A patent/NO159275C/no not_active IP Right Cessation
- 1984-10-02 DK DK471284A patent/DK154504C/da not_active IP Right Cessation
- 1984-10-03 HU HU843746A patent/HU194559B/hu unknown
- 1984-10-03 HU HU844649A patent/HU195493B/hu unknown
- 1984-10-03 CS CS847493A patent/CS253593B2/cs unknown
- 1984-10-04 YU YU1708/84A patent/YU43381B/xx unknown
- 1984-10-04 IT IT22981/84A patent/IT1218850B/it active
- 1984-10-04 PT PT79326A patent/PT79326B/pt not_active IP Right Cessation
- 1984-10-05 ES ES536544A patent/ES8505937A1/es not_active Expired
- 1984-10-05 CA CA000464861A patent/CA1246066A/en not_active Expired
- 1984-10-05 AT AT0316384A patent/AT387775B/de active
- 1984-10-05 SU SU843805901A patent/SU1405703A3/ru active
- 1984-10-05 BE BE0/213782A patent/BE900758A/fr not_active IP Right Cessation
- 1984-10-05 DD DD84268074A patent/DD224594A5/de not_active IP Right Cessation
- 1984-10-05 SE SE8405002A patent/SE460789B/sv not_active IP Right Cessation
- 1984-10-05 PL PL1984249918A patent/PL143957B1/pl unknown
-
1986
- 1986-08-27 YU YU1496/86A patent/YU43603B/xx unknown
-
1989
- 1989-01-24 SE SE8900248A patent/SE464411B/sv not_active IP Right Cessation
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