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HRID 4073作成日:2026年10月23日

4-Methylpiperidine → 9-Methyl-6-(4-methyl-1-piperidinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine

https://huagongshe.com/ja/reaction/4073

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylpiperidineHCID 69381—
反応物9-Methyl-1,2dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepin-6-oneHCID 13823284—
触媒Titanium TetrachlorideHCID 24193—
溶媒TolueneHCID 1140—
生成物9-Methyl-6-(4-methyl-1-piperidinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepineHCID 13823304—

反応手順

A stirred mixture of 6.26 g (0.0250 mole) of 9-methyl-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepin-6-one and 1000 ml of toluene was heated under nitrogen until a solution resulted. Then there was added 24.8 g (0.250 mole) of 4-methylpiperidine, followed by 14.2 g (0.075 mole) of titanium tetrachloride. The mixture was heated under reflux for three 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 8.1 g (98%) of product. Recrystallization from ethyl acetate provided the analytical sample, mp 194°-196° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04723003
出典データセットuspto-grants-1988_02
ORD IDord-f7516339756740c0a28c8861e84e7229
出典メモuspto-grants-1988_02