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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811061Generated: November 2, 2026

3-Bromo-4-fluoroaniline → N-(3-Bromo-4-fluorophenyl)-N′-(4-methyl-2-thiazolyl)urea

https://huagongshe.com/reaction/1811061

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-4-fluoroanilineHCID 2779286—
ReactantHCID 59691744HCID 59691744—
SolventTetrahydrofuranHCID 8028—
ProductN-(3-Bromo-4-fluorophenyl)-N′-(4-methyl-2-thiazolyl)ureaHCID 59375115—

Reaction Steps

Step 2 A solution of 3-bromo-4-fluoroaniline (250 mg, 1.316 mmol) in THF (6 mL) was stirred on ice and treated with TEA (0.367 mL, 2.63 mmol), then with phenyl 4-methylthiazol-2-ylcarbamate (308 mg, 1.316 mmol) and the resulting solution was stirred at rt for 70 h. The mixture was concentrated and the residue was stirred in 1 M hydrochloric acid, forming a precipitate which was collected by filtration, rinsed with water and dried under vacuum to provide 1-(3-bromo-4-fluorophenyl)-3-(4-methylthiazol-2-yl)urea as an off white solid (400 mg, 92%). 1H NMR (400 MHz, DMSO-d6) δ 9.62 (s, 1H) 7.94 (dd, J=6.3, 2.5 Hz, 1H) 7.37-7.45 (m, 1H) 7.32 (t, J=8.7 Hz, 1H) 6.67 (d, J=1.1 Hz, 1H) 2.23 (d, J=1.1 Hz, 3H). Mass spectrum m/z 330, 332 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362065B2
Source datasetuspto-grants-2013_01
ORD IDord-02b32923a38e42a38a1ffdad2ed3b994
Source noteuspto-grants-2013_01