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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879208Generated: November 2, 2026

4-Fluorobenzylamine → 2-Bromo-N-(4-fluorobenzyl)-4-methylthiazole-5-carboxamide

https://huagongshe.com/reaction/1879208

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzylamineHCID 67326—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant2-Bromo-4-methyl-1,3-thiazole-5-carboxylic acidHCID 2824058—
SolventDichloromethaneHCID 6344—
Product2-Bromo-N-(4-fluorobenzyl)-4-methylthiazole-5-carboxamideHCID 6663140591.1%

Reaction Steps

To a solution of 2-bromo-4-methyl-thiazole-5-carboxylic acid (10.0 g, 45.0 mmol) in methylene chloride (200 mL) was added 4-fluoro-benzylamine (6.19 g, 49.5 mmol), benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (21.9 g, 49.5 mmol) and N,N-diisopropylethylamine (15.7 mL, 90.1 mmol) and the mixture was stirred under nitrogen at room temperature for 16 hr. The reaction mixture was diluted with methylene chloride (300 mL), washed with water (300 mL) and brine (2×200 mL). The organic phase was dried (Na2SO4) and evaporated. The residue was purified by flash chromatography over silica gel (methylene chloride:methanol, 95:5) to provide 2-bromo-4-methyl-thiazole-5-carboxylic acid 4-fluoro-benzylamide as a beige solid (13.5 g, 90% yield). MS (M+H)+=330; Rt=136 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314138B2
Source datasetuspto-grants-2012_11
ORD IDord-866c3c41b7fa4601b90a55878728d959
Source noteuspto-grants-2012_11