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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1162214생성일: 2026년 10월 25일

Pyridinium chloride → 4-{[1-(pyridin-2-ylmethyl)-1H-indazol-5-yl]amino}quinazolin-5-ol

https://huagongshe.com/reaction/1162214

반응식

참여 물질

역할이름HCID투입량
반응물Pyridinium chlorideHCID 10176127—
반응물5-methoxy-N-[1-(pyridin-2-ylmethyl)-1H-indazol-5-yl]quinazolin-4-amineHCID 68618792—
용매PyridineHCID 1049—
생성물4-{[1-(pyridin-2-ylmethyl)-1H-indazol-5-yl]amino}quinazolin-5-olHCID 136346719100.1%

반응 단계

A mixture of 5-methoxy-N-[1-(pyridin-2-ylmethyl)-1H-indazol-5-yl]quinazolin-4-amine (10.1 g, 27.4 mmol) and pyridine hydrochloride (15.8 g, 137 mmol) in pyridine (150 ml) was heated at reflux for 3 hours. After cooling and evaporation of the solvents, the residue was triturated in 5% aqueous sodium bicarbonate and the resulting mixture was stirred for 30 minutes. The yellowish precipitate was filtered, washed with water and ether, and dried over P2O5 under high vacuum to give 4-{[1-(pyridin-2-ylmethyl)-1H-indazol-5-yl]amino}quinazolin-5-ol as a solid (10.1 g, 100%); NMR spectrum 5.76 (s, 2H), 6.67 (m, 2H), 6.96 (d, 1H), 7.29 (m, 1H), 7.42 (m, 1H), 7.52 (dd, 1H), 7.74-7.66 (m, 2H), 8.13 (s, 1H), 8.33 (s, 2H), 8.52 (d, 1H); Mass spectrum MH+ 369.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07820683B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-0dc5c2fc1e21469b9b7b905462872429
출처 메모uspto-grants-2010_10