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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69173생성일: 2026년 10월 23일

Ethanolamine → 2-(3-Imidazo[1,2-a]pyridin-6-ylmethyl-imidazo[1,2-b]pyridazin-6-ylamino)-ethanol

https://huagongshe.com/ko/reaction/69173

반응식

참여 물질

역할이름HCID투입량
반응물EthanolamineHCID 700—
반응물Potassium FluorideHCID 522689—
반응물6-Chloro-3-imidazo[1,2-a]pyridin-6-ylmethyl-imidazo[1,2-b]pyridazineHCID 44208571—
용매Ethyl AcetateHCID 8857—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물2-(3-Imidazo[1,2-a]pyridin-6-ylmethyl-imidazo[1,2-b]pyridazin-6-ylamino)-ethanolHCID 57917357—

반응 조건

온도180 °C

반응 단계

Ethanolamine (277 μL, 4.55 mmol) was added to a solution of (6-Chloro-3-imidazo[1,2-a]pyridin-6-ylmethyl-imidazo[1,2-b]pyridazine (Example 74, 65 mg, 0.228 mmol) and KF (67 mg, 1.138 mmol) in NMP (1.5 mL). The RM was stirred at 180° C. for 2 h. The mixture was diluted with EtOAc and washed with 1 M Na2CO3 (1×) and water (3×). The aqueous layer was extracted with EtOAc (×2). The combined organic layer was dried over Na2SO4, filtered and concentrated. The aqueous phase was further extracted with DCM (4×). The organic layer was then dried over Na2SO4, filtered and concentrated. The combined residues were purified by preparative LCMS to afford the title compound as a yellow oil (tR 2.62 min (conditions 4), MH+=309.1, 1H-NMR in DMSO-d6: 8.84 (s, 1H); 8.28 (d, 1H); 8.16 (d, 1H); 7.95 (m, 3H); 7.86 (s, 1H); 7.72 (m, 1H); 7.16 (d, 1H); 4.40 (s, 2H); 3.52 (t, 2H); 3.32 (m, 2H)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822468B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-44bf633d8ed549dd8e7ffb5933bfb9cc
출처 메모uspto-grants-2014_09