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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975156Generated: November 2, 2026

Sodium borohydride → HCID 18920285, compound

https://huagongshe.com/reaction/1975156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-(4-(2-(2-Ethoxyethoxy)ethoxy)-1,2,5-thiadiazol-3-yl)-1-methylpyridinium iodideHCID 19075326—
SolventEthanolHCID 702—
ProductHCID 18920285HCID 18920285—

Reaction Conditions

Temperature-10 °C

Reaction Steps

Sodium borohydride (230 mg, 6 mmol) was added to a solution of 3-(4-(2-(2-ethoxyethoxy)ethoxy)-1,2,5-thiadiazol-3-yl)-1-methylpyridinium iodide (3 mmol) in ethanol (99.9%, 20 ml) and the reaction mixture was stirred at -10° C. for 1 h. After evaporation the residue was dissolved in water and extracted with ethyl acetate. The dried organic phases were evaporated and the residue purified by column chromatography (SiO2, eluent: ethyl acetate/methanol (4:1)). The title compound was crystallized as the oxalate salt from acetone to yield 290 mg. (M.p. 115°-116° C.; M+ : 313; Compound 43).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05284859
Source datasetuspto-grants-1994_02
ORD IDord-c1311019a7714f4cac81dd9d2818539e
Source noteuspto-grants-1994_02