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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734554Generated: November 2, 2026

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/1734554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethanesulfonic AcidHCID 6395—
Reactant2-(Ethylthio)ethanolHCID 8075—
ReactantSodium HydroxideHCID 14798—
Reactant3-(4-(2-Ethylthio-1-ethoxy)-1,2,5-thiadiazol-3-yl)pyridineHCID 19612583—
Product1,2,5,6-Tetrahydro-1-methyl-3-(3-(2-ethylsulfinyl-1-ethoxy)-1,2,5-thiadiazol-4-yl)pyridine oxalateHCID 19612597—

Reaction Steps

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 NaIO4 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 45.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534528
Source datasetuspto-grants-1996_07
ORD IDord-f3a4571638d140a5ab719d432dee0c69
Source noteuspto-grants-1996_07