HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-Fluoro-N-((1R,3S)-3-hydroxycyclohexyl)-5-(4-(trifluoromethyl)phenyl)isoxazole-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | (1S,3R)-3-aminocyclohexanol | HCID 25630532 | — |
| Reactant | 4-Fluoro-5-(4-(trifluoromethyl)phenyl)isoxazole-3-carboxylic acid | HCID 67121067 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Fluoro-N-((1R,3S)-3-hydroxycyclohexyl)-5-(4-(trifluoromethyl)phenyl)isoxazole-3-carboxamide | HCID 25181772 | — |
Reaction Steps
To a solution of 4-fluoro-5-(4-(trifluoromethyl)phenyl)isoxazole-3-carboxylic acid (19 mg, 0.07 mmol), (1S,3R)-3-aminocyclohexanol (9.3 mg, 0.081 mmol), 1-hydroxybenzotriazole hydrate (9.0 mg, 0.07 mmol), and triethylamine (10 μL, 0.07 mmol) in tetrahydrofuran (1 mL) was added N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (15 mg. 0.081 mmol). After stirring overnight, the volatiles were removed in vacuo and the compound was purified by silica gel chromatography eluting with 5% methanol in dichloromethane to afford the title compound: (12.1 mg, 0.03 mmol). MS (ESI) m/z (M+H+): 373.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08211927B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-4ecf6e5eb09741ea90b01d60b4de2ba4 |
| Source note | uspto-grants-2012_07 |