HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexylamine → HCID 25212109, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 5-(4-Methyl-5-trifluoromethyl-isoxazol-3-yl)-thiophene-2-carboxylic acid | HCID 25210997 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 25212109 | HCID 25212109 | — |
Reaction Steps
Prepared from 5-(5-Trifluoromethyl-4-methyl-isoxazol-3-yl)-thiophene-2-carboxylic acid and cyclohexylamine by the method described in Example 2 Method B reversing the order of addition such that intermediate solid acid chloride was added to a THF solution of triethylamine and piperidine derivative. Colorless solid (80 mg, 89%). 1H NMR (CDCl3) 1.18-1.36 (m, 1H), 1.36-1.50 (m, 1H), 1.60-1.82 (m, 4H), 1.98-2.10 (m, 2H), 2.37 (d, J=0.9, 3H), 3.90-4.04 (m, 1H), 5.88 (br d, J=7.0, 1H), 7.49 (d, J=4.0, 1H), 7.51 (d, J=3.5, 1H). 19F NMR −63.36. LC/MS 7.18 min, [M+1]+ 359.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08921399B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-842c0a66b17e4bcc81f3ec1c769c3af2 |
| Source note | uspto-grants-2014_12 |