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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8721생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/8721

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1-Benzyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridine dihydrochlorideHCID 21983657—
반응물2-Chloro-6,7-dimethoxy-3H-quinazolin-4-oneHCID 135456664—
용매WaterHCID 962—
용매2-MethoxyethanolHCID 8019—
생성물2-(1-benzyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-6,7-dimethoxy-3H-quinazolin-4-oneHCID 13572350829.9%

반응 조건

온도120 °C

반응 단계

A mixture of 2-chloro-6,7-dimethoxy-3H-quinazolin-4-one 1 (wherein R is methyl and Z is —C(O)—, 296 mg, 1.24 mmol), 1-benzyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridine dihydrochloride 15a (440 mg, 1.54 mmol)) and diisopropylethylamine (1.2 g, 9.26 mmol) in 2-methoxyethanol (10 mL) was stirred at 120° C. for 6 hours. The reaction mixture was concentrated in vacuo to give an oil residue, which was diluted with water. The white precipitate that formed was collected by filtration to give 155 mg of 2-(1-benzyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-6,7-dimethoxy-3H-quinazolin-4-one 501, [M+H]+=418.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091200B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-1072292ad8ec44c99727818e337ae56f
출처 메모uspto-grants-2006_08