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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 2,2-Difluoro-1,3-dioxaindan-4-amine | HCID 2736891 | — |
| 반응물 | N-BOC-N,N-Bis(2-chloroethyl)amine | HCID 11230235 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-(2,2-Difluoro-benzo[1,3]dioxol-4-yl)-piperazine-1-carboxylic acid tert-butyl ester | HCID 69417487 | 22.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07160888B2 |
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| 출처 데이터셋 | uspto-grants-2007_01 |
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| ORD ID | ord-8e099b4593f5486a974eba2aa0e3f8f2 |
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| 출처 메모 | uspto-grants-2007_01 |
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