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HRID 494093作成日:2026年10月26日

Butyl vinyl ether → Ethyl 6-acetyl-8-(benzyloxy)-2-methyl-1-oxo-1,2,3,4-tetrahydro-pyrrolo[1,2-a]-pyrazine-7-carboxylate

https://huagongshe.com/reaction/494093

反応式

関与物質

役割名称HCID仕込み量
反応物Butyl vinyl etherHCID 8108—
反応物thallium(I) acetateHCID 11247—
反応物1,3-Bis(diphenylphosphino)propaneHCID 81219—
反応物DiisopropylethylamineHCID 81531—
反応物Ethyl 8-(benzyloxy)-6-bromo-2-methyl-1-oxo-1,2,3,4-tetrahydro-pyrrolo[1,2-a]-pyrazine-7-carboxylateHCID 68866169—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
生成物Ethyl 6-acetyl-8-(benzyloxy)-2-methyl-1-oxo-1,2,3,4-tetrahydro-pyrrolo[1,2-a]-pyrazine-7-carboxylateHCID 68866335—

反応条件

温度100 °C

反応手順

A mixture of ethyl 8-(benzyloxy)-6-bromo-2-methyl-1-oxo-1,2,3,4-tetrahydro-pyrrolo[1,2-a]-pyrazine-7-carboxylate (0.42 g, 1.03 mmol), palladium acetate (29 mg, 0.13 mmol), thallium acetate (0.34 g, 1.29 mmol), diisopropyl ethylamine (0.58 mL, 4.12 mmol), 1,3-bis(diphenylphosphino)propane (60 mg, 0.14 mol), n-butyl vinyl ether (0.67 mL, 5.2 mmol) in DMF (3 mL) was purged with nitrogen for 5 minutes. The mixture was sealed and heated at 100° C. overnight. The reaction mixture was concentrated under vacuum, and the residue was treated with 1 N aq HCl and stirred at room temperature for one hour. The reaction mixture was diluted with dichloromethane. The organic extract was dried over sodium sulfate, filtered and concentrated. The residue was subjected to column chromatography on silica gel eluted with ethyl acetate to provide titled product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07538112B2
出典データセットuspto-grants-2009_05
ORD IDord-d37487c3c657462abd88c53ff7dd2cf2
出典メモuspto-grants-2009_05