돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 494093생성일: 2026년 10월 25일

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

반응식

참여 물질

역할이름HCID투입량
반응물Butyl vinyl etherHCID 8108—
반응물thallium(I) acetateHCID 11247—
반응물1,3-Bis(diphenylphosphino)propaneHCID 81219—
반응물DiisopropylethylamineHCID 81531—
반응물Ethyl 8-(benzyloxy)-6-bromo-2-methyl-1-oxo-1,2,3,4-tetrahydro-pyrrolo[1,2-a]-pyrazine-7-carboxylateHCID 68866169—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물Ethyl 6-acetyl-8-(benzyloxy)-2-methyl-1-oxo-1,2,3,4-tetrahydro-pyrrolo[1,2-a]-pyrazine-7-carboxylateHCID 68866335—

반응 조건

온도100 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07538112B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-d37487c3c657462abd88c53ff7dd2cf2
출처 메모uspto-grants-2009_05