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HRID 57841作成日:2026年10月26日

2-(Tributylstannyl)pyrazine → Tert-butyl 4-[6-(6-pyrazin-2-ylpyrazolo[4,3-c]pyridin-1-yl)-2-pyridyl]piperazine-1-carboxylate

https://huagongshe.com/reaction/57841

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Tributylstannyl)pyrazineHCID 2737316—
反応物Tert-butyl 4-[6-(6-chloropyrazolo[4,3-c]pyridin-1-yl)-2-pyridyl]piperazine-1-carboxylateHCID 86707015—
溶媒DimethylacetamideHCID 31374—
生成物Tert-butyl 4-[6-(6-pyrazin-2-ylpyrazolo[4,3-c]pyridin-1-yl)-2-pyridyl]piperazine-1-carboxylateHCID 8670704568.2%

反応条件

温度150 °C

反応手順

A solution of tert-butyl 4-[6-(6-chloropyrazolo[4,3-c]pyridin-1-yl)-2-pyridyl]piperazine-1-carboxylate (40 mg, 0.096 mmol) and palladium(0)tetrakis(triphenylphosphine) (11 mg, 0.0095 mmol) in N,N-dimethylacetamide 1 mL was added (2-pyrazinyl)tributyltin (0.064 mL, 0.19 mmol). The reaction mixture heated at 150° C. for 45 min in biotage microwave. The reaction mixture was filtered through celite and concentrated. The crude product was diluted with EtOAc then washed with water. The organic layers was dried with sodium sulfate, filtered, and concentrated in vacuum. The crude product was purified by flash chromatography (EtOAc/Heptane eluted at 20% EtOAc) to give tert-butyl 4-[6-(6-pyrazin-2-ylpyrazolo[4,3-c]pyridin-1-yl)-2-pyridyl]piperazine-1-carboxylate 30 mg 67% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434725B2
出典データセットuspto-grants-2016_09
ORD IDord-2d095c942d9e4872930c9e0b4bb48297
出典メモuspto-grants-2016_09