SU253070A1 - - Google Patents
Info
- Publication number
 - SU253070A1 SU253070A1 SU1261301A SU1261301A SU253070A1 SU 253070 A1 SU253070 A1 SU 253070A1 SU 1261301 A SU1261301 A SU 1261301A SU 1261301 A SU1261301 A SU 1261301A SU 253070 A1 SU253070 A1 SU 253070A1
 - Authority
 - SU
 - USSR - Soviet Union
 - Prior art keywords
 - dimethyl
 - pyrrole
 - carboxylic acid
 - methanol
 - mol
 - Prior art date
 
Links
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
 - DOYOPBSXEIZLRE-UHFFFAOYSA-N pyrrole-3-carboxylic acid Chemical compound OC(=O)C=1C=CNC=1 DOYOPBSXEIZLRE-UHFFFAOYSA-N 0.000 description 6
 - RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
 - VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
 - CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
 - 150000001875 compounds Chemical class 0.000 description 2
 - ICJYWDHNTMJKFP-UHFFFAOYSA-N ethyl 1h-pyrrole-3-carboxylate Chemical compound CCOC(=O)C=1C=CNC=1 ICJYWDHNTMJKFP-UHFFFAOYSA-N 0.000 description 2
 - 238000000034 method Methods 0.000 description 2
 - 238000002360 preparation method Methods 0.000 description 2
 - PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
 - 239000013543 active substance Substances 0.000 description 1
 - -1 aniline ketones Chemical class 0.000 description 1
 - 230000015572 biosynthetic process Effects 0.000 description 1
 - 238000006243 chemical reaction Methods 0.000 description 1
 - 239000013078 crystal Substances 0.000 description 1
 - OLYAZPRGVAYQKH-UHFFFAOYSA-N ethyl 4-amino-2-methylthiophene-3-carboxylate;hydrochloride Chemical compound Cl.CCOC(=O)C=1C(N)=CSC=1C OLYAZPRGVAYQKH-UHFFFAOYSA-N 0.000 description 1
 - 125000004494 ethyl ester group Chemical group 0.000 description 1
 - 239000000543 intermediate Substances 0.000 description 1
 - 238000002955 isolation Methods 0.000 description 1
 - 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
 - 235000019341 magnesium sulphate Nutrition 0.000 description 1
 - 150000003233 pyrroles Chemical class 0.000 description 1
 - 239000011541 reaction mixture Substances 0.000 description 1
 - 239000002904 solvent Substances 0.000 description 1
 - 239000000126 substance Substances 0.000 description 1
 - 238000003786 synthesis reaction Methods 0.000 description 1
 - XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
 
Landscapes
- Pyrrole Compounds (AREA)
 
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| SU1261301A SU253070A1 (en:Method) | 1968-07-30 | 1968-07-30 | 
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| SU1261301A SU253070A1 (en:Method) | 1968-07-30 | 1968-07-30 | 
Publications (1)
| Publication Number | Publication Date | 
|---|---|
| SU253070A1 true SU253070A1 (en:Method) | 1969-09-30 | 
Family
ID=91899536
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| SU1261301A SU253070A1 (en:Method) | 1968-07-30 | 1968-07-30 | 
Country Status (1)
| Country | Link | 
|---|---|
| SU (1) | SU253070A1 (en:Method) | 
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| WO2022173722A1 (en) * | 2021-02-09 | 2022-08-18 | Gilead Sciences, Inc. | Thienopyrrole compounds | 
| US12070455B2 (en) | 2021-09-10 | 2024-08-27 | Gilead Sciences, Inc. | Thienopyrrole compounds | 
- 
        1968
        
- 1968-07-30 SU SU1261301A patent/SU253070A1/ru active
 
 
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| WO2022173722A1 (en) * | 2021-02-09 | 2022-08-18 | Gilead Sciences, Inc. | Thienopyrrole compounds | 
| US12070455B2 (en) | 2021-09-10 | 2024-08-27 | Gilead Sciences, Inc. | Thienopyrrole compounds | 
Similar Documents
| Publication | Publication Date | Title | 
|---|---|---|
| Morgan et al. | Some derivatives of cis-3, 6-endomethylene-Δ4-tetrahydrophthalic acid | |
| SU253070A1 (en:Method) | ||
| SU490290A3 (ru) | Способ получени производных пиримидин-6- ил -ацетоксиаминовой кислоты | |
| Weis | 3, 4, 5-Tricyanopyrazole | |
| JP3317309B2 (ja) | 3−置換アミノ−4,4,4−トリフルオロクロトン酸エステルの製造法 | |
| SU422138A3 (en:Method) | ||
| Noyce et al. | Studies of Configuration. V. The Preparation and Configuration of cis-3-Methoxycyclopentanecarboxylic Acid | |
| US2478047A (en) | Alpha-amino-beta, beta-diethoxypropionic acid and process for preparation | |
| SU507225A3 (ru) | Способ получени - пропионил-4-оксипролина или его солей | |
| SU1313856A1 (ru) | Способ получени производных цис- или транс-диаминодибензоилдибензо-18-краун-6 | |
| SU478833A1 (ru) | Способ получени производных тиено -(3,2-в)-пиррола | |
| RU2059610C1 (ru) | Способ получения 3-арил-6-ариламиноантрапиридонов | |
| SU446506A1 (ru) | Способ получени производных 4-аминохиназолинов | |
| SU487878A1 (ru) | Способ получени -дифенил- -пикрилгидразина | |
| SU368265A1 (ru) | Способ получения 4-алкил-5,6-диоксипиразоло- | |
| SU1205756A3 (ru) | Способ получени 1,1-дихлор-4-метилпентадиенов | |
| SU759507A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ (Ь^д^-ТЕТРАЦИАНКЕТОНОВ | |
| SU369116A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ СПИРО-р-ДИКЕТОЛАКТОНОВ ИНДАНДИОНОВОГО РЯДА | |
| Redemann et al. | The Characterization of Indole-3-acetic Acid and its Esters1 | |
| SU794007A1 (ru) | Способ получени 5-арил-4-карбоксиме-ТилиМидАзОлОНОВ-2 | |
| SU370205A1 (ru) | Способ получения производных пирона-2 | |
| SU279622A1 (ru) | Способ получени 3-(5"-нитро-2"-фурфурилиденамино)-2-оксазолидона(фуразолидона) | |
| SU332720A1 (ru) | Способ получени 1-амино-2-ароил-4-хлорантрахинонов | |
| JP2004189624A (ja) | 3,3−ジメチルシクロプロパン−1,2−ジカルボン酸無水物の製造方法 | |
| US3810941A (en) | Plicatamides |