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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421308Generated: October 26, 2026

Ammonia → 2-(Carbamoylamino)thiophene-3-carboxamide

https://huagongshe.com/reaction/2421308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantTrichloroacetyl isocyanateHCID 76400—
Reactant2-Aminothiophene-3-carboxamideHCID 699495—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
Product2-(Carbamoylamino)thiophene-3-carboxamideHCID 11171402—

Reaction Steps

2-Amino-3-thiophenecarboxamide (0.44 g) was suspended in acetonitrile (25 ml) and trichloroacetylisocyanate (0.2 ml) added dropwise with stirring over 10 minutes. Stirring was continued for a further 3 h at room temperature and then a solution of ammonia in methanol (10 ml of a 2M solution) was added and stirring continued for a further 2 h. The solvent was evaporated and the residue treated with water. The resultant solid was filtered off and washed with more water. Trituration with ether gave the title urea (0.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956084B2
Source datasetuspto-grants-2011_06
ORD IDord-3671e59bf1c34f11a1b3efbacb0105d8
Source noteuspto-grants-2011_06