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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69654생성일: 2026년 10월 24일

Triphenyl phosphite → Methyl 6-oxo-5,6,6a,7,9,10-hexahydropyrido[3,2-e][1,4]thiazino[4,3-a]pyrazine-3-carboxylate

https://huagongshe.com/ko/reaction/69654

반응식

참여 물질

역할이름HCID투입량
반응물Triphenyl phosphiteHCID 7540—
반응물Ethyl 4-(5-(methoxycarbonyl)-3-nitropyridin-2-yl)thiomorpholine-3-carboxylateHCID 58324448—
반응물HCID 178418361HCID 178418361—
촉매PlatinumHCID 23939—
촉매Ammonium metavanadateHCID 516859—
용매DichloromethaneHCID 6344—
생성물Methyl 6-oxo-5,6,6a,7,9,10-hexahydropyrido[3,2-e][1,4]thiazino[4,3-a]pyrazine-3-carboxylateHCID 5832451496%

반응 단계

Ethyl 4-(5-(methoxycarbonyl)-3-nitropyridin-2-yl)thiomorpholine-3-carboxylate (600 mg g, 1.69 mmol) was dissolved in dichloromethane (5 mL). To the yellow solution was added ammonium metavanadate (10.0 mg, 0.085 mmol), triphenyl phosphite (aprox 10 ul, 0.032 mmol), and Pt/C (50 mg, 5% w/w). The reaction mixture was pressurized with hydrogen gas (110 psi) and stirred at room temperature for 16 h. The reaction was then depressurized and diluted with dichloromethane (20 mL) which was refluxed for 30 min. The hot solution was filtered through a pad of celite and washed with hot dichloromethane (3×10 mL). The filtrate was concentrated to yield the title compound (452 mg, 96%) as a white solid. [M+H] calc'd for C12H13N3O3S, 280; found, 280.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822470B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d6c5adeceb984594ad6d4b9103b9e17e
출처 메모uspto-grants-2014_09