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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 454064생성일: 2026년 10월 25일

Potassium Carbonate → 6-Methoxy-4-(2-methylindol-5-yloxy)-7-(3-piperidinopropoxy)quinazoline

https://huagongshe.com/reaction/454064

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-methyl-1H-indol-5-olHCID 83336—
반응물4-Chloro-6-methoxy-7-(3-(piperidin-1-YL)propoxy)quinazolineHCID 11002191—
용매DimethylformamideHCID 6228—
생성물6-Methoxy-4-(2-methylindol-5-yloxy)-7-(3-piperidinopropoxy)quinazolineHCID 2203054054.8%

반응 조건

온도85 °C

반응 단계

A solution of 4-chloro-6-methoxy-7-(3-piperidinopropoxy)quinazoline (100 mg, 0.29 mmol), 5-hydroxy-2-methylindole (53 mg, 0.36 mmol), (prepared as described for the starting material in Example 48), and potassium carbonate (62 mg, 0.44 mmol) in DMF (2 ml) was heated at 85° C. for 3 hours, followed by heating at 95° C. for 2 hours. After cooling, ice/water (15 ml) was added and the precipitate was collected by filtration and dried under vacuum. The solid was purified by column chromatography eluting with methylene chloride/methanol (95/5) followed by methylene chloride/methanol/3M ammonia in methanol (95/3/2) to give 6-methoxy-4-(2-methylindol-5-yloxy)-7-(3-piperidinopropoxy)quinazoline (71 mg, 54%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492560B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-4cda509b26934e589b358b50bdc162a4
출처 메모uspto-grants-2013_07