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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702406Generated: October 30, 2026

Sodium Methoxide → HCID 178512709, compound

https://huagongshe.com/reaction/1702406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactant3,4-Dimethoxy-1,2,5-thiadiazole 1-oxideHCID 12913947—
ReactantHCID 178478806HCID 178478806—
SolventMethanolHCID 887—
ProductHCID 178512709HCID 178512709—

Reaction Steps

To a solution of sodium methoxide (2.16 g; 40.0 mmoles) in 100 ml of CH3OH that was cooled to 0° in an ice-water bath was added 2-[(2-guanidinothiazol-4-yl)methylthio]ethylamine dihydrochloride (6.09 g; 20.0 mmoles) and, after 20 minutes of stirring, the solution was treated with 3,4-dimethoxy-1,2,5-thiadiazole 1-oxide (1.62 g; 10 mmoles). The reaction mixture was stirred at ambient temperature for 65 hours and evaporated under reduced pressure. The residue was chromatographed on 100 g of silica gel (230-400 mesh) by flash chromatography using a gradient elution of acetonitrile-methanol. The appropriate fractions were combined, evaporated and the residue chromatographed on a Preparative HPLC system using μ-porasil silica gel. The appropriate fractions were combined, and evaporated under reduced pressure to give the title compound as an amorphous solid; the NMR spectrum (100 MHz) in d6 dimethyl sulfoxide showed the presence of approximately 0.11 mole of ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04380639
Source datasetuspto-grants-1983_04
ORD IDord-1c0a22a14ddf444a947e82b6578fbe9a
Source noteuspto-grants-1983_04