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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898963Generated: 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/1898963

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 numberUS05571826
Source datasetuspto-grants-1996_11
ORD IDord-0859ad19deed425bb7ba3988b5054935
Source noteuspto-grants-1996_11