化工社化工社 化学情報印刷レポート · 研究参考用
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
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)amine | HCID 21951963 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | (1-Benzyl-1H-indazol-5-yl)-(6-(5-(1,3-dioxolan-2-yl)-furan-2-yl)-quinazolin-4-yl)-amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06713485B2 |
| 出典データセット | uspto-grants-2004_03 |
| ORD ID | ord-9f56845b44114838a0df0d67b5834dec |
| 出典メモ | uspto-grants-2004_03 |