関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Bromo-4-chloroaniline | HCID 70110 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Triphosgene | HCID 94429 | — |
| 反応物 | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-[(4-Boc-piperazin-1-ylcarbonyl)amino]-5-chlorobromobenzene | HCID 21906538 | 191.1% |
反応手順
To a stirring solution of triphosgene (2.7 g, 9.0 mmol) in dichloromethane (100 mL) was added, dropwise via an addition funnel, a solution of 2-bromo-4-chloroaniline (5 g, 24.2 mmol) and N,N-diisopropylethylamine (6.9 g, 53.2 mmol) in dichloromethane (50 mL). After complete addition and an additional hour, a solution of N-Boc-piperazine (5 g, 26.6 mmol) in dichloromethane (50 mL) was added. After stirring overnight, the solvent was removed in vacuo and the residue was partitioned between ethyl acetate and water. The organic phase was separated and washed consecutively with 1 M citric acid, brine, sat. aq sodium bicarbonate and finally with brine, then dried with MgSO4, filtered and concentrated in vacuo. The residue was then dissolved in a minimal amount of chloroform and chromatographed over silica gel, eluting with 20% ethyl acetate in hexanes followed by 30% ethyl acetate in hexanes. The product containing fractions were combined and concentrated in vacuo and the resulting solid was suspended in diethyl ether, sonicated and then filtered and dried in vacuo to give 7.2 g (71%) of a white powder.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US06635657B1 |
|---|
| 出典データセット | uspto-grants-2003_10 |
|---|
| ORD ID | ord-d7e4e3d9262843f78eda677a727a6669 |
|---|
| 出典メモ | uspto-grants-2003_10 |
|---|