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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1366200생성일: 2026년 10월 25일

Diisopropylethylamine → (5-Bromo-imidazo[1,2-a]pyrazin-8-yl)-[4-(1-isopropylpiperidin-4-yl)-phenyl]amine

https://huagongshe.com/reaction/1366200

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물5,8-Dibromoimidazo[1,2-a]pyrazineHCID 53485949—
반응물4-(1-Isopropylpiperidin-4-yl)anilineHCID 57590071—
용매IsopropanolHCID 3776—
생성물(5-Bromo-imidazo[1,2-a]pyrazin-8-yl)-[4-(1-isopropylpiperidin-4-yl)-phenyl]amineHCID 59023125—

반응 단계

N,N-Diisopropylethylamine (360 μL, 2.2 mmol) is added to a mixture of 4-(1-isopropylpiperidin-4-yl)phenylamine (220 mg, 1.0 mmol) and 5,8-dibromoimidazo[1,2-a]pyrazine (280 mg, 1.0 mmol) in iPrOH (5 mL) and heated at reflux for 48 h. The mixture is cooled and the solvent evaporated under reduced pressure to afford an orange-brown solid. This is partitioned between DCM (50 mL) and water (20 mL) and the layers are separated. The organic phase is washed with citric acid (10% aq., 3×25 mL). The combined washings are extracted with DCM (25 mL) and then made basic by addition of NaHCO3 (s). The mixture is extracted with DCM (3×25 mL) and the combined extracts dried over MgSO4 and evaporated. The material is used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07893058B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-6e6bfda52336489ba3c3c91266b46816
출처 메모uspto-grants-2011_02