参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 4-甲基六氢吡啶 | HCID 69381 | — |
| 反应物 | 9-Bromo-1,2dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine-6-one | HCID 13823283 | — |
| 催化剂 | 四氯化钛 | HCID 24193 | — |
| 溶剂 | 甲苯 | HCID 1140 | — |
| 产物 | 9-Bromo-6-(4-methyl-1-piperidinyl)-1,2-dihydrobenzo[b]pyrrolo-[3,2,1-jk][1,4]benzodiazepine | HCID 13823303 | 83% |
反应步骤
A mixture of 4.73 g (0.0150 mole) of 9-bromo-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepin-6-one and 1000 ml of toluene was heated under nitrogen, with stirring, until a solution resulted. Then there was added 14.9 g (0.150 mole) of 4-methylpiperidine, followed by 8.54 g (0.045 mole) of titanium tetrachloride. The mixture was refluxed for 3 hours, cooled to room temperature and filtered. The filtrate was stirred with 500 ml of 2N sodium hydroxide solution for 15 minutes and the layers were separated. The aqueous phase was extracted with 250 ml of toluene. The toluene layers were combined, washed once with 2N sodium hydroxide solution, twice with water, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to an oil which solidified. The solid was triturated twice with hexane to afford 4.9 g (83%) of product. Recrystallization from ethyl acetate provided the analytical sample, mp 177°-179° C.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 专利号 | US04723007 |
|---|
| 来源数据集 | uspto-grants-1988_02 |
|---|
| ORD ID | ord-2914492a9d1346ff9a2310b39c27edd6 |
|---|
| 来源说明 | uspto-grants-1988_02 |
|---|