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HRID 57884作成日:2026年10月26日

Tricyclohexylphosphine → 6-(6-Methylpyrazin-2-yl)-1-tetrahydropyran-2-yl-pyrazolo[4,3-c]pyridine

https://huagongshe.com/reaction/57884

反応式

関与物質

役割名称HCID仕込み量
反応物TricyclohexylphosphineHCID 75806—
反応物2-Chloro-6-methylpyrazineHCID 7170095—
反応物Tributyl-(1-tetrahydropyran-2-ylpyrazolo[4,3-c]pyridin-6-yl)stannaneHCID 86707078—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒DimethylacetamideHCID 31374—
生成物6-(6-Methylpyrazin-2-yl)-1-tetrahydropyran-2-yl-pyrazolo[4,3-c]pyridineHCID 8670707764.5%

反応条件

温度130 °C

反応手順

A mixture of tributyl-(1-tetrahydropyran-2-ylpyrazolo[4,3-c]pyridin-6-yl)stannane (7.139 mmol; 3514.5 mg), 2-chloro-6-methyl-pyrazine (10.71 mmol; 1377 mg), tricyclohexylphosphine; (0.5140 mmol; 144.1 mg) and tris(dibenzylideneacetone)dipalladium (0) (0.2142 mmol; 196.1 mg) in N,N-Dimethylacetamide (15 mL) was purged with Argon for 1 min. The reaction mixture was sealed in a pressure vial and heated at 130° C. overnight. The mixture was partitioned between EtOAc and water. The organic layer was concentrated and the residue was purified on silica eluted with 0 to 100% EtOAc in DCM to afford 6-(6-methylpyrazin-2-yl)-1-tetrahydropyran-2-yl-pyrazolo[4,3-c]pyridine as a clear oil (1.3608 g, 60%).

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-81aad0fd0aaf44388e143b3bd8f47840
出典メモuspto-grants-2016_09