HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 6-(Piperidine-1-sulfonyl)-4-trifluoromethyl-1H-quinolin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Oxo-4-trifluoromethyl-1,2-dihydroquinoline-6-sulfonyl chloride | HCID 22055310 | — |
| Product | 6-(Piperidine-1-sulfonyl)-4-trifluoromethyl-1H-quinolin-2-one | HCID 9975771 | 43.4% |
Reaction Steps
Condensation of 2-oxo-4-trifluoromethyl-1,2-dihydroquinoline-6-sulfonyl chloride (Preparation 3, 50 mg, 160 μmol) with piperidine (17 μL, 168 μmol), employing NEt3 (23 μL, 168 μmol) as base as outlined for Example 1, gave the title compound (25 mg, 42%): δH ((CD3)2SO)=1.30–1.40 (m, 2H), 1.50–1.60 (m, 4H), 2.90 (t, 4H), 7.15 (s, 1H), 7.60 (d, 1H), 7.90–8.00 (m, 2H); m/z (ES+)=361.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07064207B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-16a38e69766745078a40ebe3cd14c86d |
| Source note | uspto-grants-2006_06 |