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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 603205생성일: 2026년 10월 26일

Tert-butyl 3-oxopyrrolidine-1-carboxylate → Tert-butyl 3-(4-{[(3,4-dichlorophenyl)amino]carbonyl}piperazin-1-yl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/603205

반응식

참여 물질

역할이름HCID투입량
반응물Tert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물N-(3,4-Dichlorophenyl)piperazine-1-carboxamideHCID 16775732—
용매DichloromethaneHCID 6344—
생성물Tert-butyl 3-(4-{[(3,4-dichlorophenyl)amino]carbonyl}piperazin-1-yl)pyrrolidine-1-carboxylateHCID 5765674088%

반응 단계

N-(3,4-dichlorophenyl)piperazine-1-carboxamide (0.548 g, 2 mmols) and 1-N—BOC-3-pyrrolidinone (370 mg, 2 mmols) were stirred at room temperature in dichloromethane (20 ml) for approximately 15 minutes. Added to this mixture was sodium triacetoxyborohydride (1.06 g, 5 mmols) and the reaction stirred overnight at room temperature. Saturated sodium bicarbonate solution (5 ml) was added and the mixture stirred for 1 hour then poured onto a hydromatrix column and the product eluted with dichloromethane (100 ml). The crude product was subjected to chromatography on silica gel (50 g) using a gradient of 100% dichloromethane through to 10% methanolic ammonia in dichloromethane to give the title compound as a white solid (780 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07906645B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-f15c540206774f6cad9de25bfde0b674
출처 메모uspto-grants-2011_03