HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479846Generated: October 26, 2026
Diethyl Pyrocarbonate → 1-[ethyl-(4-fluorophenyl)sulfonyl-amino]-N-[[2-[4-(trifluoromethyl)phenyl]-4-pyridyl]methyl]cyclopropanecarboxamide
https://huagongshe.com/reaction/1479846
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Pyrocarbonate | HCID 3051 | — |
| Reactant | [2-(4-Trifluoromethyl-phenyl)-pyridin-4-yl]methylamine | HCID 68758847 | — |
| Reactant | 1-[Ethyl-(4-fluorophenyl)sulfonyl-amino]cyclopropanecarboxylic acid | HCID 90384363 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[ethyl-(4-fluorophenyl)sulfonyl-amino]-N-[[2-[4-(trifluoromethyl)phenyl]-4-pyridyl]methyl]cyclopropanecarboxamide | HCID 90384185 | 26.8% |
Reaction Steps
Acid 15A (303 mg, 1 mmol) was dissolved in 5 ml of THF and at rt DEPC (1.1 equiv, 0.17 ml) and [2-[4-(trifluoromethyl)phenyl]-4-pyridyl]methanamine 21A (1.1 equiv., 277.5 mg) were added to the solution. The mixture was stirred at rt overnight then evaporated. he residue was dissolved in AcOEt (30 ml) and washed with water (1×20 ml) and brine. The organic phase was dried over sodium sulfate and concentrated under vacuum. The purification of the crude by chromatographic column (1:1 EtOAc:Petroleum ether) afforded 140 mg of a white solid. Yield=26.8% 1HNMR (DMSO, 400 MHz) δ 1.09 (2H, bs), 1.23 (3H, t, J=7.2 Hz), 1.40 (2H, bs), 3.40 (2H, q, J=6.8 Hz), 4.41 (2H, bs), 7.26 (1H, dd), 7.42 (2H, t, J=8.8 Hz), 7.87 (4H, m), 7.98 (1H, bs), 8.30 (3H, bd), 8.64 (1H, dd, J=4.8 Hz) [M+1] 521.9 (C25H23F4N3O3S requires 521.53).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409864B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-40b66184ffaf4aba94adb4a358c76b95 |
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| Source note | uspto-grants-2016_08 |
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