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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892500Generated: October 26, 2026

5-{2-[2-(Acetylamino)-1,3-thiazol-4-yl]vinyl}thiophene-2-carboxylic acid → 5-{2-[2-(Acetylamino)-1,3-thiazol-4-yl]ethyl}thiophene-2-carboxylic acid

https://huagongshe.com/reaction/1892500

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-{2-[2-(Acetylamino)-1,3-thiazol-4-yl]vinyl}thiophene-2-carboxylic acidHCID 86650005—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product5-{2-[2-(Acetylamino)-1,3-thiazol-4-yl]ethyl}thiophene-2-carboxylic acidHCID 8665000681.4%

Reaction Steps

5-{2-[2-(Acetylamino)-1,3-thiazol-4-yl]vinyl}thiophene-2-carboxylic acid (900.0 mg, 3.058 mmol) was dissolved in a mixed solvent of tetrahydrofuran (250 ml) and methanol (100 ml). 20% Palladium carbon was added, and the mixture was hydrogenated at room temperature under 4 atm. After the completion of the reaction, the reaction mixture was filtered through celite, and the filtrate was concentrated under reduced pressure. Diethyl ether (100 ml) was added to the concentrated residue, and the precipitate was collected by filtration, washed with diethyl ether, and dried under reduced pressure to give 5-{2-[2-(acetylamino)-1,3-thiazol-4-yl]ethyl}thiophene-2-carboxylic acid (738.1 mg, 2.490 mmol, yield 81.4%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507690B2
Source datasetuspto-grants-2013_08
ORD IDord-6c950cf75ba840c38818ccc0ebcef983
Source noteuspto-grants-2013_08