Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908187Generated: October 31, 2026

Methanesulfonic Acid → Methyl 3-(5-amino-1,3,4-thiadiazol-2-yl)propanoate

https://huagongshe.com/reaction/908187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantButanoic acid, 4-chloro-4-oxo-, methyl esterHCID 73888—
ReactantThiosemicarbazideHCID 2723789—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-(5-amino-1,3,4-thiadiazol-2-yl)propanoateHCID 54474128—

Reaction Steps

3-Chlorocarbonyl-propionic acid methyl ester (4.4 g, 21 mmol) is added dropwise to a stirred suspension of thiosemicarbazide (4.0 g, 44 mmol) in THF (25 ml) at 0° C. After stirring at room temperature for 18 h the product which precipitates is removed by filtration and washed with diethyl ether. This product (7.1 g, 34 mmol) is suspended in toluene (30 ml) at 0° C. and methane sulfonic acid (3.37 ml, 52 mmol) is added dropwise to the stirred reaction. The reaction is heated at 70° C. for 3 hours then concentrated at reduced pressure. Methanol (30 ml) is added followed by slow addition of aqueous ammonia, with stirring, until the solution is basic. The titled compound which precipitates is removed by filtration and purified by chromatography on silica, eluting with chloroform-methanol (10:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017608B2
Source datasetuspto-grants-2011_09
ORD IDord-0a714bcfb4764588b3f0b05006714a1c
Source noteuspto-grants-2011_09