関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triphosgene | HCID 94429 | — |
| 反応物 | Methyl 3,4-diamino-5-methylthiophene-2-carboxylate | HCID 18693138 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Methyl 1,3-dihydro-4-methyl-2-oxo-thieno[3,4-d]imidazole-6-carboxylate | HCID 18693187 | 4,777.4% |
反応手順
Methyl 3,4-diamino-5-methylthiophene-2-carboxylate (3.0 g) was dissolved in a mixture of N,N-dimethyl formamide (5 ml) and dichloromethane (15 ml). To the solution was added triphosgene (2.4 g) in portions. The mixture was stirred for two days at room temperature, and precipitates were collected by filtration, washed with dichloromethane and dried. Resultant white powder (2.4 g) was suspended in N,N-dimethylformamide (25 ml). To the suspension was added sodium hydride (60% in oil; 0.55 g), and the mixture was stirred for three days at room temperature. The solvent was evaporated under reduced pressure. To the residue was added 2N-HCl. Resulting precipitates were collected by filtration, washed with water, ether and methanol successively, followed by drying to afford the title compound (82 g, 53%) as pale brown powder.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06100252 |
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| 出典データセット | uspto-grants-2000_08 |
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| ORD ID | ord-fa368a6f8ed04cd79d82b177fe8d5de0 |
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| 出典メモ | uspto-grants-2000_08 |
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