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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 454172생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/454172

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물3-methyl-1H-indol-5-olHCID 192734—
반응물4-Chloro-6-methoxy-7-(3-(piperidin-1-YL)propoxy)quinazolineHCID 11002191—
용매DimethylacetamideHCID 31374—
생성물6-Methoxy-4-(3-methylindol-5-yloxy)-7-(3-piperidinopropoxy)quinazolineHCID 2203090569.4%

반응 조건

온도100 °C

반응 단계

A mixture of 4-chloro-6-methoxy-7-(3-piperidinopropoxy)quinazoline (168 mg, 0.5 mmol), (prepared as described for the starting material in Example 67), potassium carbonate (207 mg, 1.5 mmol), 3-methyl-5-hydroxyindole (88 mg, 0.6 mmol), (Can. J. Chem. 1964, 42, 514), and DMA (2.0 ml) was purged with nitrogen for 5 minutes at 25° C. This mixture was then stirred at 100° C. for 3 hours then allowed to cool to ambient temperature, was filtered and the filtrate evaporated under vacuum. The residue was purified by silica column chromatography eluting with dichloromethane/methanolic ammonia (7M) (90/10) to give 6-methoxy-4-(3-methylindol-5-yloxy)-7-(3-piperidinopropoxy)quinazoline (155 mg, 69%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492560B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-e46e77ec694543c79f851034faddb33e
출처 메모uspto-grants-2013_07