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HRID 355004作成日:2026年10月23日

Oxatomide → ethyl 3-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-2,3-dihydro-2-oxo-1H-benzimidazole-1-acetate

https://huagongshe.com/ja/reaction/355004

反応式

関与物質

役割名称HCID仕込み量
反応物OxatomideHCID 4615—
反応物Ethyl bromoacetateHCID 7748—
反応物Sodium hydrideHCID 24758—
反応物Dibenzo-18-crown-6HCID 26541—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物ethyl 3-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-2,3-dihydro-2-oxo-1H-benzimidazole-1-acetateHCID 20506279—

反応条件

温度90 °C

反応手順

To a stirred mixture of 9.4 parts of 1-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-1,3-dihydro-2H-benzimidazol-2-one and 180 parts of methylbenzene are added 0.8 parts of sodium hydride dispersion 75% and the whole is stirred and heated for 60 minutes at 90° C. After cooling to 30° C., 0.2 parts of 2,3,11,12-dibenzo-1,4,7,10,13,16-hexaoxacyclooctadeca-2,11-diene are added and stirring is continued for 10 minutes. Then there are added 4.2 parts of ethyl 2-bromoacetate and the mixture is stirred and refluxed overnight. The reaction mixture is cooled to 90° C., 50 parts of water are added and the layers are separated while hot. The organic phase is evaporated, yielding 10 parts of ethyl 3-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-2,3-dihydro-2-oxo-1H-benzimidazole-1-acetate as a residue.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04377578
出典データセットuspto-grants-1983_03
ORD IDord-f9a30eb59e6e43e79f8199ccf9f2b38f
出典メモuspto-grants-1983_03