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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 244363생성일: 2026년 10월 26일

Water → Tert-butyl 4-(2-chloro-5-nitrophenylsulfonyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/244363

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Ethyl AcetateHCID 8857—
반응물2-Chloro-5-nitrobenzenesulfonyl chlorideHCID 20630—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
용매DichloromethaneHCID 6344—
생성물Tert-butyl 4-(2-chloro-5-nitrophenylsulfonyl)piperazine-1-carboxylateHCID 5926081683.1%

반응 단계

A solution of compound 37 (0.600 g, 2.34 mmol) in DCM (20.00 mL) was added tert-butyl 1-piperazinecarboxylate (0.566 g, 3.04 mmol) and TEA (0.422 mL, 3.04 mmol). The reaction was monitored with TLC (25% EtOAc in hexanes, Rf=0.53). The reaction mixture was complete after stirring at room temperature for 1 hr, as indicated by the absence of the starting material (TLC). Water was added and aqueous layer was extracted twice with DCM. Combined extracts were sequentially washed with water and brine, dried over MgSO4, filtered, and evaporated in vacuo to afford a yellow solid. The solid was triturated with DCM and hexanes, and then filtered to yield compound 38 as a yellow solid (0.789 g, 100% HPLC purity, 83% yield). 1H NMR (500 MHz, DMSO-d6): δ 8.60 (d, J=3 Hz, 1H), 8.47 (dd, J1=3 Hz, J2=8 Hz, 1H), 8.01 (d, J=8 Hz, 1H), 3.37 (m, 4H), 3.23 (m, 4H), 1.37 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658642B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-078429561bef4952be1dfa8c2e9147db
출처 메모uspto-grants-2014_02