戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 645704作成日:2026年10月27日

Tetravinylstannane → 2-chloro-N-(1H-indazol-6-yl)-5-vinyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine

https://huagongshe.com/reaction/645704

反応式

関与物質

役割名称HCID仕込み量
反応物TetravinylstannaneHCID 66189—
反応物2-chloro-N-(1H-indazol-6-yl)-5-iodo-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 86628040—
触媒HCID 178418397HCID 178418397—
溶媒DimethylformamideHCID 6228—
生成物2-chloro-N-(1H-indazol-6-yl)-5-vinyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 8662804129.6%

反応条件

温度60 °C

反応手順

To a solution of 2-chloro-N-(1H-indazol-6-yl)-5-iodo-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (0.45 g, 0.8 mmol) in dimethylformamide (2.0 mL) was added tetravinyltin (0.29 mL, 1.6 mmol) and tetrakis(triphenylphosphine)palladium(0) (Pd(PPh3)4) (0.092 g, 0.08 mmol). After degassing, the mixture was heated at 60° C. for 15 h. before it was diluted with EtOAc, and washed sequentially with Sat. NaHCO3 and brine. The organic extract was dried over Na2SO4 and concentrated to give a crude residue. Purification by flash column chromatography (Hexane/EtOAc=1:1) gave 2-chloro-N-(1H-indazol-6-yl)-5-vinyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (0.11 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07705004B2
出典データセットuspto-grants-2010_04
ORD IDord-f5ee33c6b49a4a03a14cc86261f53e97
出典メモuspto-grants-2010_04