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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2077902생성일: 2026년 10월 24일

Potassium Carbonate → (R)-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/2077902

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Methyl 6-chloro-5-nitronicotinateHCID 346961—
반응물(R)-thiomorpholine-3-carboxylic acidHCID 1152541—
촉매Triphenyl phosphiteHCID 7540—
촉매PlatinumHCID 23939—
촉매Ammonium metavanadateHCID 516859—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물(R)-methyl 6-oxo-5,6,6a,7,9,10-hexahydropyrido[3,2-e][1,4]thiazino[4,3-a]pyrazine-3-carboxylateHCID 5832449752%

반응 단계

To a suspension of (R)-thiomorpholine-3-carboxylic acid (1.009 g, 6.86 mmol) in THF was added methyl 6-chloro-5-nitronicotinate (1.35 g, 6.23 mmol) and potassium carbonate (2.58 g, 18.70 mmol). The suspension was heated to reflux for 3 hours. The crude orange solution was allowed to cool to RT and filtered through a pad of celite which was washed with DCM (50 mL), and transferred to a bomb hydroginator. To the solution was added triphenyl phosphite (0.019 ml, 0.061 mmol), platinum (0.238 g, 0.061 mmol), and ammonium metavanadate. The vessel was sealed and pressurized to 140 psi with stirring for 24 h at room temperature. The vessel was depressurized and the mixture was diluted with DCM (100 mL) and refluxed for 30 minutes. The hot mixture was filtered through celite and concentrated to yield 887 mg (52%) of the product as a white solid. [M+H] calc'd for C12H13N3O3S, 280; found, 280.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07928105B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-ee95950f0704451bafcec53547580f32
출처 메모uspto-grants-2011_04