HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate → N-(4-Chloro-3-nitrobenzyl)-1-(trifluoromethyl)cyclopropanecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | 1-(Trifluoromethyl)cyclopropane-1-carboxylic acid | HCID 2778306 | — |
| Reactant | (4-Chloro-3-nitrophenyl)methanamine | HCID 18796740 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-Chloro-3-nitrobenzyl)-1-(trifluoromethyl)cyclopropanecarboxamide | HCID 59529820 | — |
Reaction Steps
TBTU (0.44 g, 1.4 mmol) and TEA (0.43 mL, 3.1 mmol) were added to 1-trifluoromethyl-cyclopropanecarboxylic acid (0.19 g, 1.2 mmol) in THF (5 mL). After 10 min at rt 4-chloro-3-nitro-benzylamine (0.23 g, 1.2 mmol) was added to the reaction mixture and stirring was continued overnight. The mixture was concentrated, diluted with EtOAc and washed with sat.aq. NaHCO3-solution, water and brine. The organic layer was dried over Na2SO4 and concentrated to give the subtitle compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08466186B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-dc1932b53c6f4cc3becb0ae023112c59 |
| Source note | uspto-grants-2013_06 |