Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356696Generated: November 1, 2026

Trifluoroacetic acid → Methyl 2-[3-(4-fluoro-3-thiophen-2-ylphenyl)ureido]-2-methylpropionate

https://huagongshe.com/reaction/2356696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
ReactantMethyl 3-isocyanato-2-methylpropanoateHCID 13063727—
Reactant4-Fluoro-3-(thiophen-2-yl)anilineHCID 57829334—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-[3-(4-fluoro-3-thiophen-2-ylphenyl)ureido]-2-methylpropionateHCID 57829328—

Reaction Steps

According to process “A′”, 0.12 g of the trifluoroacetic acid salt of compound 267.4 was dissolved at room temperature in 5 ml of dry tetrahydrofuran, admixed with 0.17 ml of triethylamine and then admixed dropwise with a solution of 0.10 g of methyl isocyanatomethylpropionate in 2 ml of dry tetrahydrofuran. The mixture was stirred at room temperature for 2 hours. For workup, the mixture was concentrated under reduced pressure, and the residue was stirred with water, filtered, washed with water and dried. Methyl 2-[3-(4-fluoro-3-thiophen-2-ylphenyl)ureido]-2-methylpropionate (267.3) was obtained. Molecular weight 336.39 (C16H17FN2O3S); retention time Rt=1.46 min. [F]; MS (ESI): 337.05 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759366B2
Source datasetuspto-grants-2010_07
ORD IDord-1116b2eebb9949b598d40de9eade8f96
Source noteuspto-grants-2010_07