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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381345Generated: October 31, 2026

Hydrochloric Acid → 2-Methoxyimino-2-(5-formamido-1,2,4-thiadiazol-3-yl)acetic acid

https://huagongshe.com/reaction/1381345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium BicarbonateHCID 516892—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
ReactantHCID 13577105HCID 13577105—
SolventMethanolHCID 887—
Product2-Methoxyimino-2-(5-formamido-1,2,4-thiadiazol-3-yl)acetic acidHCID 54428012—

Reaction Steps

A mixture of S-methyl (5-formamido-1,2,4-thiadiazol-3-yl)thioglyoxylate (231 mg) in methanol (2 ml) and 1N-aqueous solution of potassium hydroxide (3.5 ml) was stirred for an hour at ambient temperature. The mixture was adjusted to pH 7.6 with 1N hydrochloric acid, followed by an addition of O-methylhydroxylamine hydrochloride (90 mg) and stirring for 30 minutes at ambient temperature. The reaction mixture was neutralized with an aqueous solution of sodium bicarbonate and concentrated to remove methanol. The concentrated aqueous solution was adjusted to pH 4 with hydrochloric acid and washed with ethyl acetate. The aqueous layer was adjusted to pH 1 with hydrochloric acid, saturated with sodium chloride and extracted with ethyl acetate. The extract was evaporated to dryness and the residue was triturated with diethyl ether, collected by filtration and then dried to give the title compound (80mg), mp. 185° to 186° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585872
Source datasetuspto-grants-1986_04
ORD IDord-7e0d34e4a76741ffb962f447d755e96c
Source noteuspto-grants-1986_04