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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178584Generated: November 4, 2026

Triethylamine → [5-(2-Fluoro-4-pyridyl)-4-(3-methylphenyl)-1,3-thiazol-2-yl]amine

https://huagongshe.com/reaction/1178584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromineHCID 24408—
ReactantSodium BicarbonateHCID 516892—
ReactantThioureaHCID 2723790—
Reactant2-(2-Fluoro-4-pyridyl)-1-(3-methylphenyl)ethanoneHCID 11543157—
SolventAcetic AcidHCID 176—
SolventAcetonitrileHCID 6342—
Product[5-(2-Fluoro-4-pyridyl)-4-(3-methylphenyl)-1,3-thiazol-2-yl]amineHCID 987896335%

Reaction Steps

Bromine (1.9 mL, 37 mmol) was added to a solution of 2-(2-fluoro-4-pyridyl)-1-(3-methylphenyl)ethanone (8.5 g, 37 mmol) in acetic acid (50 mL) and the mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated. Triethylamine (5.2 mL, 37 mmol) was added to a mixture of this residue and thiourea (3.0 g, 40 mmol) in acetonitrile (50 mL) and the mixture was stirred at 80° C. for 2 hours. A saturated aqueous solution of sodium hydrogencarbonate (50 mL) was added to the reaction mixture and the precipitated solid was collected by filtration. After the resulting solid was washed with water, it was dried. The crude crystals were recrystallized from ethanol to obtain 3.7 g (yield 35%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276527B2
Source datasetuspto-grants-2007_10
ORD IDord-0816b81333f34ffbbfc2d4c8153b9f26
Source noteuspto-grants-2007_10