HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Pyrocarbonate → 1-[(4-fluorophenyl)sulfonyl-methyl-amino]-N-[[3-[4-(trifluoromethoxy)phenyl]phenyl]methyl]cyclopropanecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Pyrocarbonate | HCID 3051 | — |
| Reactant | (4'-(Trifluoromethoxy)-[1,1'-biphenyl]-3-yl)methanamine | HCID 61032752 | — |
| Reactant | 1-[Methyl-(4-fluorophenyl)sulfonyl-amino]cyclopropanecarboxylic acid | HCID 90390806 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[(4-fluorophenyl)sulfonyl-methyl-amino]-N-[[3-[4-(trifluoromethoxy)phenyl]phenyl]methyl]cyclopropanecarboxamide | HCID 90390309 | 15% |
Reaction Steps
Acid 15A (350 mg, 1.28 mmol) was dissolved in 5 ml of THF and at rt DEPC (0.25 mL, 1.3 mol eq) and [3-[4-(trifluoromethoxy)phenyl]phenyl]methanamine 23B (0.376 g, 1.1 mol eq) 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 (3:7 EtOAc:Petroleum ether) afforded 100 mg of a white solid. Yield=15% 1HNMR (DMSO, 200 MHz) δ 1.09 (2H, bs), 1.34 (2H, bs), 3.00 (3H, s), 4.35 (2H, d, J=5.8 Hz), 7.43 (8H, m), 7.81 (4H, m), 8.17 (1H, bt); [M+1] 523.9 (C25H22F4N2O4S requires 522.51).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409864B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-fc6c2268e4a844958a98cf101247b83c |
| Source note | uspto-grants-2016_08 |