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Ammonia → tert-Butyl (5-bromo-2-carbamoylthiophen-3-yl)carbamate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| 反応物 | 5-Bromo-3-((tert-butoxycarbonyl)amino)thiophene-2-carboxylic acid | HCID 21975854 | — |
| 反応物 | HCID 178418300 | HCID 178418300 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | tert-Butyl (5-bromo-2-carbamoylthiophen-3-yl)carbamate | HCID 21975856 | — |
反応手順
5-Bromo-3-[(t-butyloxycarbonyl)amino]thiophene-2-carboxylic acid (0.80 g) was stirred in acetonitrile (80 ml). Hydroxybenztriazole (1.41 g) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (2.62 g) were added and stirring continued at room temperature for 10 minutes. Concentrated aqueous ammonia solution (8 ml) was added and the reaction mixture was heated to reflux for 1 h. The acetonitrile was removed by evaporation. Water (100 ml) was added and the mixture was sonicated and triturated. The resultant off-white solid was then collected by filtration, washed with water and dried under vacuum (0.763 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07098240B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-0290ac04ad0e445e81e62a6c3df508c9 |
| 出典メモ | uspto-grants-2006_08 |