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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 244100생성일: 2026년 10월 25일

Ammonia → 3-Cyclobutyl-1-quinolin-7-ylimidazo[1,5-a]pyrazin-8-ylamine

https://huagongshe.com/reaction/244100

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Acetone cardiceHCID 18522661—
반응물7-(8-Chloro-3-cyclobutylimidazo[1,5-a]pyrazin-1-yl)-quinolineHCID 57680887—
용매2-Propanol, reaction products with ammonia, distn. residuesHCID 18331942—
생성물3-Cyclobutyl-1-quinolin-7-ylimidazo[1,5-a]pyrazin-8-ylamineHCID 44451337—

반응 조건

온도110 °C

반응 단계

Gaseous NH3 was condensed into a cooled (dry ice/acetone) solution of 7-(8-chloro-3-cyclobutylimidazo[1,5-a]pyrazin-1-yl)-quinoline (203.2 mg, 0.607 mmol) in 2M NH3/iPrOH (6 mL) in a pressure tube until the volume was doubled, then the tube was sealed and heated to 110° C. (bath temp.) for 19 h. The ammonia was evaporated, the crude material was adsorbed onto Hydromatrix and chromatographed on silica gel [Jones Flashmaster, 10 g/70 mL cartridge, eluting with CH2Cl2 1:1 (1-6)→2% MeOH in CH2Cl2 (7-27)→4% MeOH in CH2Cl2 (28-37)→5% MeOH in CH2Cl2 (38-53)→7% MeOH in CH2Cl2 (54-67)], yielding the title compound as a yellow solid, >98% pure by HPLC, mp. 94-96° C.; 1H NMR (CDCl3, 400 MHz) δ 2.00-2.10 (m, 1H), 2.12-2.25 (m, 1H), 2.47-2.57 (m, 2H), 2.61-2.73 (m, 2H), 3.85 (quint, J=8.4 Hz, 1H), 5.23 (brs, 2H), 7.10 (d, J=4.4 Hz, 1H), 7.16 (d, J=4.4 Hz, 1H), 7.44 (dd, J=4.2, 8.2 Hz, 1H), 7.95 (d, J=8.4 Hz, 1H), 8.00 (d, J=8.4 Hz, 1H), 8.22 (d, J=8.2 Hz, 1H), 8.36 (s, 1H), 8.95-9.00 (m, 1H); MS (ES+): m/z 316.2 (30) [MH+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653268B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-3db5713f9d3e46d1a7254d30c05ee967
출처 메모uspto-grants-2014_02