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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9444생성일: 2026년 10월 25일

tert-Butyl 4-(2-aminoethyl)piperazine-1-carboxylate → Tert-butyl 4-[2-(7-bromo-3-nitroquinolin-4-ylamino)ethyl]piperazine-1-carboxylate

https://huagongshe.com/reaction/9444

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl 4-(2-aminoethyl)piperazine-1-carboxylateHCID 1514400—
반응물7-Bromo-4-chloro-3-nitroquinolineHCID 21984361—
생성물Tert-butyl 4-[2-(7-bromo-3-nitroquinolin-4-ylamino)ethyl]piperazine-1-carboxylateHCID 2198415459.8%

반응 단계

7-Bromo-4-chloro-3-nitroquinoline (33.0 g, 115 mmol) was treated with 4-(2-aminoethyl)-1-(tert-butoxycarbonyl)piperazine (26.4 mL, 115 mmol) according to the method described in Part E of Example 1. The reaction was stirred overnight. The crude product was triturated with diethyl ether and isolated by filtration to provide 33.05 g of tert-butyl 4-[2-(7-bromo-3-nitroquinolin-4-ylamino)ethyl]piperazine-1-carboxylate as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091214B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-ed6c6d0d8e3d4c479e339443c4683a34
출처 메모uspto-grants-2006_08