HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883132Generated: October 26, 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 2-amino-N-(4-fluorobenzyl)-4-methylthiazole-5-carboxamide
https://huagongshe.com/reaction/883132
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 4-Fluorobenzylamine | HCID 67326 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Amino-4-methyl-thiazole-5-carboxylic acid | HCID 832243 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-amino-N-(4-fluorobenzyl)-4-methylthiazole-5-carboxamide | HCID 55115203 | 80% |
Reaction Steps
To a solution of 2-amino-4-methylthiazole-5-carboxylic acid (4.20 g, 26.0 mmol) in anhydrous N,N-dimethylformamide (100 mL) was added 1-hydroxybenzotriazole (9.30 g, 69.0 mmol), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide (6.60 g, 34.0 mmol), diisopropylethylamine (4.40 g, 34.0 mmol), and (4-fluorophenyl)methanamine (3.97 g, 32.0 mmol). The reaction mixture was stirred at ambient temperature for 18 hours and N,N-dimethylformamide was removed in vacuo. The residue was dissolved in ethyl acetate (400 mL) and washed with saturated aqueous sodium bicarbonate (2×100 mL) and brine (100 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated in vacuo to afford the title compound as a yellowish solid in 80% yield (5.60 g): 1H NMR (300 MHz, CDCl3) δ 7.39-7.17 (m, 2H), 7.01 (t, J=8.3 Hz, 2H), 5.78 (br s, 1H), 5.34 (br s, 2H), 4.50 (d, J=5.6 Hz, 2H), 2.47 (s, 3H); MS (ES+) m/z 266.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08236835B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-fbf0d3e967df485296a2ce4573524b53 |
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| Source note | uspto-grants-2012_08 |
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