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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69623생성일: 2026년 10월 25일

Triphenyl phosphite → (S)-methyl 6-oxo-6,6a,7,8,9,10-hexahydro-5H-dipyrido[1,2-a:3',2'-e]pyrazine-3-carboxylate

https://huagongshe.com/reaction/69623

반응식

참여 물질

역할이름HCID투입량
반응물Triphenyl phosphiteHCID 7540—
반응물(S)-methyl 6-(2-(methoxycarbonyl)piperidin-1-yl)-5-nitronicotinateHCID 58324510—
반응물HCID 178418361HCID 178418361—
촉매PlatinumHCID 23939—
촉매Ammonium metavanadate [UN2859] [Poison]HCID 62684—
용매DichloromethaneHCID 6344—
생성물(S)-methyl 6-oxo-6,6a,7,8,9,10-hexahydro-5H-dipyrido[1,2-a:3',2'-e]pyrazine-3-carboxylateHCID 5832449589%

반응 단계

In a bomb hydroginator, (S)-methyl 6-(2-(methoxycarbonyl)piperidin-1-yl)-5-nitronicotinate (1.95 g, 6.03 mmol), triphenyl phosphite (0.019 ml, 0.060 mmol), ammonium vanadate (0.056 g, 0.483 mmol) and platinum (5% on carbon, 0.235 g, 0.060 mmol) were mixed in dichloromethane (Volume: 30.2 ml) to give a suspension. The bomb was sealed and pressurized to 110 psi with hydrogen gas. The reaction was stirred at 110 psi 16 h, depressurized, diluted with DCM (100 mL) and refluxed 10 minutes. The hot mixture was filtered through celite and washed with DCM (50 mL). The filtrate was concentrated in vacuo to yield 1.4 g (89%) of the product as a white solid and used without further purification. [M+H] calc'd for C13H15N3O3, 262; found, 262.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822470B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-e5ca4146512848e68549ed74dd7bf83e
출처 메모uspto-grants-2014_09