HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067206Generated: October 26, 2026
Ethylamine hydrochloride → 2-(4-{3-[2-Chloro-4-(2,4-difluoro-phenylamino)-benzoyl]-4-methyl-phenyl}-[1,2,3]triazol-1-yl)-N-ethyl-acetamide
https://huagongshe.com/reaction/2067206
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylamine hydrochloride | HCID 11198 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Pentafluorophenyl diphenylphosphinate | HCID 4652311 | — |
| Reactant | (4-{3-[2-Chloro-4-(2,4-difluoro-phenylamino)-benzoyl]-4-methyl-phenyl}-[1,2,3]triazol-1-yl)-acetic acid | HCID 11496723 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-{3-[2-Chloro-4-(2,4-difluoro-phenylamino)-benzoyl]-4-methyl-phenyl}-[1,2,3]triazol-1-yl)-N-ethyl-acetamide | HCID 11598675 | — |
Reaction Steps
To a solution of compound 111 (39 mg, 0.08 mmol) in DMF (1.0 mL) was added ethylamine hydrochloride (20 mg, 0.08 mmol), FDPP (43 mg, 0.11 mmol), and DIEA (68 μL, 0.4 mmol). The flask was flushed with argon and the reaction mixture was stirred at RT for 72 h and then poured into a mixture of water (4 mL), HCl (4N, 2 mL), and EtOAc. The phases were separated. The organic phase was concentrated on silica in vacuo. The crude product was purified by chromatography eluting with EtOAc/petroleum ether (40-60) 50:50 to 100:0 as the eluent to afford the title compound as white foam. 13C NMR (DMSO-d6) δ 194.9, 164.8, 149.3, 145.2, 139.8, 135.9, 133.7, 133.7, 131.7, 128.2, 127.1, 126.6, 126.4 (dd), 125.0, 124.2 (dd), 123.0, 114.8, 111.9 (dd), 111.8, 105.0 (dd), 51.7, 33.6, 19.4, 14.4
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08293772B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-db3efbe32a514f558cf7b6ec85206638 |
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| Source note | uspto-grants-2012_10 |
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