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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 603248생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/603248

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물PyBOPHCID 2724699—
반응물N-(3,4-Dichlorophenyl)piperazine-1-carboxamideHCID 16775732—
반응물(2R)-1-(tert-Butoxycarbonyl)piperazine-2-carboxylic acidHCID 24820285—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
생성물N-(3,4-Dichlorophenyl)-4-{[(2R)-4-tert-butoxycarbonylpiperazin-2-yl]carbonyl}piperazine-1-carboxamideHCID 67220684—

반응 조건

온도0 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07906645B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-71bb2a4bc7e54ee7b5d2025d10f96c61
출처 메모uspto-grants-2011_03