戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 58244作成日:2026年10月25日

2-(Tributylstannyl)pyridine → 7-(1-azidoethyl)-3-methyl-6-pyridin-2-yl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one

https://huagongshe.com/reaction/58244

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Tributylstannyl)pyridineHCID 607784—
反応物7-(1-azidoethyl)-6-bromo-3-methyl-5H-thiazolo[3,2-a]pyrimidin-5-oneHCID 58111438—
触媒HCID 178418397HCID 178418397—
溶媒1,4-DioxaneHCID 31275—
生成物7-(1-azidoethyl)-3-methyl-6-pyridin-2-yl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-oneHCID 8665006613.1%

反応条件

温度65 °C

反応手順

A mixture of 2-(tributylstannyl)pyridine (Aldrich, 0.176 g, 0.382 mmol), 7-(1-azidoethyl)-6-bromo-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one (from example 8, step 3; 0.10 g, 0.318 mmol), and tetrakis(triphenylphosphine)palladium (0) (0.0184 g, 0.0159 mmol) in 1,4-dioxane (0.5 mL) was heated at 65° C. overnight. After being cooled and quenched with saturated ammonium chloride, the resulting mixture was extracted with EtOAc. The organic layers were combined, washed with brine, dried and evaporated to dryness. The residue was purified on silica gel, eluting with 0 to 100% EtOAc in hexane, to provide the desired product (13 mg, 13%). LCMS calculated for C14H13N6OS (M+H)+: m/z=313.1. Found: 313.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434746B2
出典データセットuspto-grants-2016_09
ORD IDord-30587980d95b4287b0aaa8d0fe257e0e
出典メモuspto-grants-2016_09