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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8724생성일: 2026년 10월 24일

Ethanol → 6,7-dimethoxy-2-(1-m-tolyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-3H-quinazolin-4-one

https://huagongshe.com/ko/reaction/8724

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물TriethylamineHCID 8471—
반응물1-m-tolyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridineHCID 21983644—
반응물2-Chloro-6,7-dimethoxy-3H-quinazolin-4-oneHCID 135456664—
용매1-MethoxyethanolHCID 3015637—
생성물6,7-dimethoxy-2-(1-m-tolyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-3H-quinazolin-4-oneHCID 13553251656.9%

반응 조건

온도100 °C

반응 단계

A mixture of 1-m-tolyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine 18a (100 mg, 0.5 mmol), 2-chloro-6,7-dimethoxy-3H-quinazolin-4-one 1b (100 mg, 0.4 mmol), and triethylamine (140 μL, 1.0 mmol) in 10 mL methoxyethanol was heated at 100° C. under nitrogen for 12 hr. The mixture was pumped to constant weight. The resulting residue was slurried with hot ethanol and allowed to reach ambient temperature. Vacuum filtration provided 95 mg of 6,7-dimethoxy-2-(1-m-tolyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-3H-quinazolin-4-one, 601, [M+H]+=418, as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091200B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-2c8bf22c88d141f18e9c170291be32b9
출처 메모uspto-grants-2006_08