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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1186461생성일: 2026년 10월 27일

Ethanolamine → 2-[(3-Bromoimidazo[1,2-a]pyrazin-8-yl)amino]ethan-1-ol

https://huagongshe.com/reaction/1186461

반응식

참여 물질

역할이름HCID투입량
반응물EthanolamineHCID 700—
반응물DiisopropylethylamineHCID 81531—
반응물3-Bromo-8-chloroimidazo[1,2-a]pyrazineHCID 10059849—
용매1-ButanolHCID 263—
생성물2-[(3-Bromoimidazo[1,2-a]pyrazin-8-yl)amino]ethan-1-olHCID 21070904—

반응 조건

온도100 °C

반응 단계

3-Bromo-8-chloro-imidazo[1,2-a]pyrazine (0.70 g, 3.0 mmol) (from Example 1 supra) was stirred in nBuOH (10 mL) and ethanolamine (0.22 mL, 3.65 mmol) followed by Hunig's base (1.04 mL, 6.0 mmol) Reaction mixture was then heated at 100° C. overnight. The mixture was concentrated to dryness and water was added (150 mL) followed by a saturated aqueous solution of NaHCO3 (50 mL). The reaction was then extracted with EtOAc (3×20 mL) and the organic phases were combined, washed with water (2×20 mL), dried over MgSO4 and concentrated to dryness to give 2-(3-bromo-imidazo[1,2-a]pyrazin-8-ylamino)-ethanol. (Yield 0.59 g, 77%). 1H (400 MHz; DMSO-d6) δ 3.52-3.56 (2 H, m), 3.58-3.62 (2 H, m), 4.79 (1 H, t, J=5.4 Hz), 7.42 (2 H, d, J=5 Hz), 7.56 (1 H, d, J=5 Hz), 7.66 (1 H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08673905B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-990f312e6b444a6892632f3f72f00441
출처 메모uspto-grants-2014_03