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HRID 4016生成日期:2026年10月26日

4-甲基六氢吡啶 → 9-Bromo-6-(4-methyl-1-piperidinyl)-1,2-dihydrobenzo[b]pyrrolo-[3,2,1-jk][1,4]benzodiazepine

https://huagongshe.com/reaction/4016

反应方程式

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-oneHCID 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]benzodiazepineHCID 1382330383%

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

DOI10.6084/m9.figshare.5104873.v1
专利号US04723007
来源数据集uspto-grants-1988_02
ORD IDord-2914492a9d1346ff9a2310b39c27edd6
来源说明uspto-grants-1988_02