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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1373638생성일: 2026년 10월 26일

Sodium hydride → 4-(2,2-Difluoro-benzo[1,3]dioxol-4-yl)-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1373638

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2,2-Difluoro-1,3-dioxaindan-4-amineHCID 2736891—
반응물N-BOC-N,N-Bis(2-chloroethyl)amineHCID 11230235—
용매DimethylformamideHCID 6228—
생성물4-(2,2-Difluoro-benzo[1,3]dioxol-4-yl)-piperazine-1-carboxylic acid tert-butyl esterHCID 6941748722.5%

반응 단계

An intermediate compound, 1-(2,2-Difluoro-benzo[1,3]dioxol-4-yl)-piperazine, was produced as follows: To the mixture of 2,2-difluoro-benzo[1,3]dioxol-4-ylamine (27 g, 0.156 mol) and bis-(2-chloro-ethyl)-carbamic acid tert-butyl ester (75.5 g, 0.31 mol) in DMF (500 mL) was added NaH (15.6 g, 60% oil dispersion, 0.39 mol) at 0° C. and the resulting mixture was stirred at room temperature for 24 h until LCMS indicated the starting material disappeared. The reaction was quenched with aq. NH4Cl, extracted with EtOAc, washed with brine, dried and concentrated. The residue was purified by flash chromatography (Et3N:EtOAc:heptane/1:10:100) to afford 4-(2,2-difluoro-benzo[1,3]dioxol-4-yl)-piperazine-1-carboxylic acid tert-butyl ester (12.0 g, 22%) as colorless crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07160888B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-8e099b4593f5486a974eba2aa0e3f8f2
출처 메모uspto-grants-2007_01