HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Cyclopropyl-N-piperidin-4-yl-3-(trifluoromethyl)benzenesulfonamide → HCID 57664567, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Cyclopropyl-N-piperidin-4-yl-3-(trifluoromethyl)benzenesulfonamide | HCID 2773944 | — |
| Reactant | 4,4-Bis(4-fluorophenyl)but-3-enoic acid | HCID 57664571 | — |
| Reactant | HCID 68983635 | HCID 68983635 | — |
| Product | HCID 57664567 | HCID 57664567 | — |
Reaction Steps
N-Cyclopropyl-N-{1-[4,4-bis(4-fluorophenyl)-but-3-enoyl]piperidin-4-yl}-3-trifluoromethylbenzenesulfonamide (33) was prepared by reacting N-cyclopropyl-N-piperidin-4-yl-3-trifluoromethylbenzenesulfonamide with 4,4-bis(4-fluorophenyl)-but-3-enoic acid following the procedure described for the synthesis of N-cyclopropyl-N-(2-hexenoyl)piperin-4-yl-3-trifluoromethyl-benzenesulfonamide (30) in Example 19, step a. 1H NMR (CDCl3): δ 8.12 (s, 1H), 8.03 (d, 1H), 7.86 (d, 1H), 7.71 (t, 1H), 7.15 (m, 6H), 6.96 (m, 2H), 6.21 (t, 1H), 4.68 (m, 1H), 4.02 (m, 1H), 3.61 (m, 1H), 3.15 (d, 2H), 2.93 (m, 1H), 2.51 (m, 1H), 1.93 (m, 1H), 1.69 (m, 2H), 1.25 (m, 1H), 0.90 (m, 5H). LC: 100%. MS (M+H+): 605.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09000174B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-8570792f8cfe4020ab74c05b37300a4a |
| Source note | uspto-grants-2015_04 |