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HRID 603248作成日:2026年10月27日

Sodium Bicarbonate → N-(3,4-Dichlorophenyl)-4-{[(2R)-4-tert-butoxycarbonylpiperazin-2-yl]carbonyl}piperazine-1-carboxamide

https://huagongshe.com/reaction/603248

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物PyBOPHCID 2724699—
反応物N-(3,4-Dichlorophenyl)piperazine-1-carboxamideHCID 16775732—
反応物(2R)-1-(tert-Butoxycarbonyl)piperazine-2-carboxylic acidHCID 24820285—
溶媒DimethylformamideHCID 6228—
溶媒TriethylamineHCID 8471—
生成物N-(3,4-Dichlorophenyl)-4-{[(2R)-4-tert-butoxycarbonylpiperazin-2-yl]carbonyl}piperazine-1-carboxamideHCID 67220684—

反応条件

温度0 °C

反応手順

N-(3,4-Dichlorophenyl)piperazine-1-carboxamide (596 mg) and (2R)-1-BOC-piperazine-2-carboxylic acid (500 mg) were dissolved in N,N-dimethylformamide (30 ml) and stirred at 0° C. Triethylamine (0.61 ml) was added followed by PYBOP reagent (1.13 g). The mixture was allowed to warm to room temperature overnight, poured into saturated aqueous sodium bicarbonate (60 ml) and extracted with ethyl acetate (2×100 ml), adding a little water during the process to dissolve precipitated sodium bicarbonate. The combined organic extracts were treated with brine (100 ml), dried (sodium sulphate), concentrated in vacuo and adsorbed onto silica for purification by chromatography eluting with 0-15% methanol dichloromethane. This gave the product as a white glass (710 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07906645B2
出典データセットuspto-grants-2011_03
ORD IDord-71bb2a4bc7e54ee7b5d2025d10f96c61
出典メモuspto-grants-2011_03