戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 51130作成日:2026年10月25日

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/51130

反応式

関与物質

役割名称HCID仕込み量
反応物Stannane, tributyl[5-(1,3-dioxolan-2-yl)-2-furanyl]-HCID 10960952—
反応物(1-Benzyl-1H-indazol-5-yl)-(6-bromoquinazolin-4-yl)amineHCID 21951963—
溶媒1,4-DioxaneHCID 31275—
生成物(1-Benzyl-1H-indazol-5-yl)-(6-(5-(1,3-dioxolan-2-yl)-furan-2-yl)-quinazolin-4-yl)-amineHCID 21952203—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713485B2
出典データセットuspto-grants-2004_03
ORD IDord-9f56845b44114838a0df0d67b5834dec
出典メモuspto-grants-2004_03