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2-Thiophenecarboxylic acid, 3-(isocyanatosulfonyl)-, methyl ester → 3-[[(4-Cyano-6-methoxypyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-thiophenecarboxylic acid, methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Thiophenecarboxylic acid, 3-(isocyanatosulfonyl)-, methyl ester | HCID 157296 | — |
| 反応物 | 2-Amino-6-methoxypyrimidine-4-carbonitrile | HCID 14129250 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 3-[[(4-Cyano-6-methoxypyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-thiophenecarboxylic acid, methyl ester | HCID 14129251 | — |
反応手順
2-Amino-4-cyano-6-methoxypyrimidine, 0.1 g, was mixed with 2-carbomethoxythiophene-3-sulfonyl isocyanate, 0.165 g, in 10 ml of methylene chloride. The reaction mixture was stirred at room temperature overnight. The reaction mixture was stripped to yield 0.19 g of the title compound as a solid, m.p. 89°-92° C. (dec). NMR (CDCl3): δ6.89 (s, 3H), 4.20 (s, 3H), 6.83 (s, 1H), 7.59 (d, 1H), 7.80 (d, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04740229 |
| 出典データセット | uspto-grants-1988_04 |
| ORD ID | ord-d474613647f64916ae1c47abf4f4ae76 |
| 出典メモ | uspto-grants-1988_04 |