돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2426003생성일: 2026년 10월 26일

Diisopropylethylamine → t-Butyl 4-(3-(1-(3-bromophenyl)ethylamino)-4-nitrophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2426003

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물N-(1-(3-bromophenyl)ethyl)-5-fluoro-2-nitrobenzenamineHCID 58707271—
용매AcetonitrileHCID 6342—
생성물t-Butyl 4-(3-(1-(3-bromophenyl)ethylamino)-4-nitrophenyl)piperazine-1-carboxylateHCID 5870727324.1%

반응 단계

A mixture of N-(1-(3-bromophenyl)ethyl)-5-fluoro-2-nitrobenzenamine (1.25 g, 3.7 mmol), tert-butyl piperazine-1-carboxylate (0.7 g, 3.7 mmol), diisopropylethylamine (1.0 mL, 5.7 mmol) and acetonitrile (20 mL) was heated at reflux for 18 h, cooled to room temperature and concentrated in vacuo. The residue was dissolved in ethyl acetate; this solution was washed with water, dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel using 10%-15% ethyl acetate in hexanes as eluent to yield the title compounds as a yellow solid (0.45 g, 24%). 1H NMR (400 MHz, CDCl3): δ 8.72 (d, 1 H), 8.10 (d, 1H), 7.51 (s, 1H), 7.40 (m, 1H), 7.24 (m, 2H), 6.17 (dd, 1H), 5.60 (d, 1H), 4.52 (m, 1H), 3.48 (m, 4H), 3.26 (m, 2H), 3.13 (m, 2H), 1.63 (d, 3H), 1.44 (s, 9H). MS (ESI) m/z: Calculated: 504; Observed: 505 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07968538B2
출처 데이터셋uspto-grants-2011_06
ORD IDord-35a9035c16fd4913be514fdf979d8d0f
출처 메모uspto-grants-2011_06