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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286982Generated: October 30, 2026

Bromine → Methyl 5-amino-1,2,4-thiadiazole-3-carboxylate

https://huagongshe.com/reaction/2286982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantPotassium thiocyanateHCID 516872—
ReactantSodiumHCID 5360545—
Reactant1-Ethoxycarbonylformamidine hydrobromideHCID 23316851—
SolventMethanolHCID 887—
ProductMethyl 5-amino-1,2,4-thiadiazole-3-carboxylateHCID 1357710267.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-ethoxycarbonylformamidine. hydrobromide (16.6 g.) in absolute methanol (84 ml) was added a solution of sodium (1.93 g) in absolute methanol (42 ml) at 0° C. To the mixture were added alternately bromine (12.8 g) and a solution of sodium (1.93 g) in absolute methanol (42 ml) at 0° C. and then to the suspension was added potassium thiocyanate (8.1 g) in absolute methanol (100 ml). The reaction mixture was stirred for an hour at 0° C. and for an additional 6 hours at ambient temperature. The mixture was filtered through cellulose powder and the filtrate was evaporated to dryness. The residue was dissolved in a mixture of ethyl acetate and water, and then the ethyl acetate layer was separated and dried over anhydrous magnesium sulfate. The solvent was evaporated and the residue was triturated with diethyl ether to give the title compound (9.0 g), mp. 202° to 205° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04268509
Source datasetuspto-grants-1981_05
ORD IDord-18412570489a481fa99941b017428ac0
Source noteuspto-grants-1981_05