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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1796016생성일: 2026년 10월 25일

Imidazo[1,2-a]pyrimidine, 3-(tributylstannyl)-7-(trifluoromethyl)- → 3-[6-(Pyrrolidin-1-yl)pyridin-2-yl]-7-trifluoromethylimidazo[1,2-alpha]pyrimidine

https://huagongshe.com/reaction/1796016

반응식

참여 물질

역할이름HCID투입량
반응물Imidazo[1,2-a]pyrimidine, 3-(tributylstannyl)-7-(trifluoromethyl)-HCID 11294484—
반응물2-Bromo-6-(pyrrolidin-1-yl)pyridineHCID 15470277—
생성물3-[6-(Pyrrolidin-1-yl)pyridin-2-yl]-7-trifluoromethylimidazo[1,2-alpha]pyrimidineHCID 994552726.8%

반응 단계

2-Bromo-6-(pyrrolidin-1-yl)pyridine (481 mg, 2.1 mmol) (prepared by the method of T. Sammakia et al., J. Org. Chem., 1999, 64(13), 4652-4664) was coupled to 3-tributylstannyl-7-trifluoromethylimidazo[1,2-α]pyrimidine (1.4 mmol) by the method of Example 1 to give 3-[6-(pyrrolidin-1-yl)pyridin-2-yl]-7-trifluoromethylimidazo[1,2-α]pyrimidine (125 mg) as a white solid: δH (360 MHz, DMSO) 2.02 (4H, t, J 6.5), 3.51 (4H, bs), 6.43 (1H, d, J 8.4), 7.27 (1H, d, J 7.7), 7.63 (1H, t, J 7.9), 7.71 (1H, d, J 7.4), 8.72 (1H, s), 10.51 (1H, d, J 7.4); m/z (ES+) 334 (M++H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07030128B2
출처 데이터셋uspto-grants-2006_04
ORD IDord-0214cb4ea6c045148041e4e3a15e070b
출처 메모uspto-grants-2006_04