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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Fluorobenzylamine | HCID 67326 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | 2-Bromo-4-methyl-1,3-thiazole-5-carboxylic acid | HCID 2824058 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-N-(4-fluorobenzyl)-4-methylthiazole-5-carboxamide | HCID 66631405 | 91.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314138B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-866c3c41b7fa4601b90a55878728d959 |
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| Source note | uspto-grants-2012_11 |
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