Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Thiophenecarboxylic acid, 3-(isocyanatosulfonyl)-, methyl ester → Methyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-thiophenecarboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Thiophenecarboxylic acid, 3-(isocyanatosulfonyl)-, methyl ester | HCID 157296 | — |
| 반응물 | 4-Methoxy-6-methylpyrimidin-2-amine | HCID 587236 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | Methyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-thiophenecarboxylate | HCID 13390184 | — |
반응 단계
To 1.4 g of 2-amino-4-methoxy-6-methylpyrimidine in 30 ml of anhydrous acetonitrile was added at ambient temperature, with stirring 3.6 g of 2-methoxycarbonyl-3-thiophenesulfonylisocyanate. The mixture was heated to the boiling point and then allowed to cool to ambient temperature. After stirring for sixteen hours the precipitate present in the mixture was filtered off and washed with anhydrous ethyl ether. The product thus obtained which melted at 165°-173° showed absorption peaks by infrared spectroscopy at 1720 and 1700 cm-1, consistent for the carbonyl groups in the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04701535 |
| 출처 데이터셋 | uspto-grants-1987_10 |
| ORD ID | ord-71fdcd695fb245e8be245884ebf3a9da |
| 출처 메모 | uspto-grants-1987_10 |