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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 334323생성일: 2026년 10월 26일

Potassium Carbonate → (Z)-2-(3-methoxy-4-(5-(2-methoxy-5-(3,4,5-trimethoxystyryl)phenoxy)pentyloxy)phenyl)-2,3-dihydroquinazolin-4(1H)-one

https://huagongshe.com/reaction/334323

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Combretastatin A4HCID 5351344—
반응물2-[4-(5-Bromo-pentyloxy)-3-methoxy-phenyl]-2,3-dihydro-1H-quinazolin-4-oneHCID 51042583—
용매DimethylformamideHCID 6228—
용매Ethyl acetate hexaneHCID 21226206—
생성물(Z)-2-(3-methoxy-4-(5-(2-methoxy-5-(3,4,5-trimethoxystyryl)phenoxy)pentyloxy)phenyl)-2,3-dihydroquinazolin-4(1H)-oneHCID 11768759783.4%

반응 조건

온도30 °C

반응 단계

(Z)-2-methoxy-5-(3,4,5-trimethoxystyryl)phenol (38a) (316.35 mg 1.0 mmol) in DMF (20 mL) was added anhydrous potassium carbonate (690 mg, 5.0 mmol) and 2-[4-(5-Bromo-pentyloxy)-3-methoxy-phenyl]-2,3-dihydro-1H-quinazolin-4-one (2d) (419.29 mg, 1.0 mmol). The reaction mixture was stirred at a temperature of 30° C. for 30 h and the reaction was monitored by TLC using ethyl acetate-hexane (6:4) as a solvent system. Then to this ice is added and extracted with ethyl acetate. The solvent was evaporated under vacuum to afford the crude product. This was further purified by column chromatography using ethyl acetate:hexane (6:4) as a solvent system to obtain the pure product (39d) (546 mg, 80% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883809B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-c2f30562fb904be4acfb5368de4957b3
출처 메모uspto-grants-2014_11