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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1497614생성일: 2026년 10월 25일

Stannane, tributyl[5-(1,3-dioxolan-2-yl)-2-furanyl]- → (1-Benzyl-1H-indazol-5-yl)-(6-(5-(1,3-dioxolan-2-yl)-furan-2-yl)-quinazolin-4-yl)-amine

https://huagongshe.com/reaction/1497614

반응식

참여 물질

역할이름HCID투입량
반응물Stannane, tributyl[5-(1,3-dioxolan-2-yl)-2-furanyl]-HCID 10960952—
반응물(1-Benzyl-1H-indazol-5-yl)-(6-bromoquinazolin-4-yl)amineHCID 21951963—
용매1,4-DioxaneHCID 31275—
생성물(1-Benzyl-1H-indazol-5-yl)-(6-(5-(1,3-dioxolan-2-yl)-furan-2-yl)-quinazolin-4-yl)-amineHCID 21952203—

반응 단계

Prepared according to Procedure B from (1-benzyl-1H-indazol-5-yl)-(6-bromoquinazolin-4-yl)-amine (4.3 g), 2-(tributylstannyl)-5-(1,3-dioxolan-2-yl)furan (J. Chem. Soc., Chem Commun., (1988), 560) (10 g) and 1,4-bis(diphenylphosphino) palladium (II) chloride (1 g) in dioxane. The solvent was removed in vacuo and the residue chromatographed on silica. Subsequent trituration gave the title compound δH [2H6]-DMSO 10.13 (1H, s), 8.85 (1H, s), 8.54 (1H, s), 8.20 (3H, m), 7.80 (3H, m), 7.30 (5H, m), 7.13 (1H, d), 6.79 (1H, d), 6.04 (1H, s), 5.71 (2H, s), 4.15 (4H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09199973B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-bb12d906f9294b5e8e40326e47225380
출처 메모uspto-grants-2015_12