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HRID 718058作成日:2026年10月26日

Amoxapine → (E)-ethyl 2-(4-(2-chlorodibenzo[b,f][1,4]oxazepin-11-yl)piperazin-1-yl)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/718058

反応式

関与物質

役割名称HCID仕込み量
反応物AmoxapineHCID 2170—
反応物Ethyl 2-(methylsulfonyl)pyrimidine-5-carboxylateHCID 254889—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物(E)-ethyl 2-(4-(2-chlorodibenzo[b,f][1,4]oxazepin-11-yl)piperazin-1-yl)pyrimidine-5-carboxylateHCID 59783732100.2%

反応手順

A solution of (E)-2-chloro-11-(piperazin-1-yl)dibenzo[b,f][1,4]oxazepine (0.25 g, 0.8 mmol) and ethyl 2-(methylsulfonyl)pyrimidine-5-carboxylate (0.13 g, 0.57 mmol) in DME was stirred at room temperature for 1 h. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic extract was washed with saturated aqueous solution of bicarbonate, water, acetic acid and sodium acetate (pH=4), dried over sodium sulfate and solvent evaporated. The resulting crude residue was purified by flash chromatography (0% to 30% ethyl acetate in hexane) to afford title compound 116 (0.265 g, quant.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09193749B2
出典データセットuspto-grants-2015_11
ORD IDord-10aa39fcd5194912bd39fc97cf3923fa
出典メモuspto-grants-2015_11