化工社化工社 化学情報印刷レポート · 研究参考用
Triethylamine → 4-(6,7-Dimethoxy-4-quinazolinyl)-1-piperazinethiocarboxylic acid chloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Thiophosgene | HCID 10040 | — |
| 反応物 | 6,7-Dimethoxy-4-piperazin-1-yl-quinazoline | HCID 2758484 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-(6,7-Dimethoxy-4-quinazolinyl)-1-piperazinethiocarboxylic acid chloride | HCID 10926244 | 52% |
反応手順
To a solution of 3.06 ml (40.1 mmol) of thiophosgene in 100 ml of dichloromethane were slowly added a solution of 10 g (36.5 mmol) of 6,7-dimethoxy-4-(1-piperazinyl)quinazoline obtained by the method described in South African Patent No. 67 06512 (1968) in 100 ml of dichloromethane and 12.4 ml (89.1 mmol) of triethylamine under ice-cooling. The resulting mixture was stirred at the same temperature in an atmosphere of argon for 2 hours. After the solvent was evaporated, the residue was purified by silica gel chromatography to give 6.65 g (52%) of the desired compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06750218B2 |
| 出典データセット | uspto-grants-2004_06 |
| ORD ID | ord-2443a5210f134c1d9bcb75d10d9098c5 |
| 出典メモ | uspto-grants-2004_06 |