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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 965114생성일: 2026년 10월 26일

Water → 1,2,5,6-Tetrahydro-1-methyl-3-(3-(2-ethylsulfinyl-1-ethoxy)-1,2,5-thiadiazol-4-yl)pyridine oxalate

https://huagongshe.com/reaction/965114

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Methanesulfonic AcidHCID 6395—
반응물2-(Ethylthio)ethanolHCID 8075—
반응물Sodium HydroxideHCID 14798—
반응물3-(4-(2-Ethylthio-1-ethoxy)-1,2,5-thiadiazol-3-yl)pyridineHCID 19612583—
생성물1,2,5,6-Tetrahydro-1-methyl-3-(3-(2-ethylsulfinyl-1-ethoxy)-1,2,5-thiadiazol-4-yl)pyridine oxalateHCID 19612597—

반응 단계

1,2,5,6-tetrahydro-1-methyl-3-(3-(2-ethylsulfinyl-1-ethoxy)-1,2,5-thiadiazol-4-yl)pyridine oxalate was prepared in the same manner using 2-(ethylthio)-ethanol as the starting alcohol. The intermediate 3-(4-(2-ethylthio-1-ethoxy)-1,2,5-thiadiazol-3-yl)pyridine was oxidized with 1.1 equivalent of NalO4 and 1 equivalent MeSO3H using water as the reaction solvent. After a reaction time of 3.5 h. the solution was made basic with 2N NaOH and extracted with ethyl acetate. The combined extracts were dried over MgSO4 and evaporated under vacuum. The resulting sulfoxide was then converted to the title compound in the same manner described above. M.p. 171°-172° C., M+ : 302. Compound 112.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05773452
출처 데이터셋uspto-grants-1998_06
ORD IDord-28e5ace956004f1c835c7fca41132574
출처 메모uspto-grants-1998_06