HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-(4-oxocyclohexyl)-1,3-benzoxazol-2(3H)-one → HCID 178518615, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-(4-oxocyclohexyl)-1,3-benzoxazol-2(3H)-one | HCID 9813382 | — |
| Reactant | 2-Chloro-4-fluorobenzenepropanamine | HCID 22669122 | — |
| Product | HCID 178518615 | HCID 178518615 | 21% |
Reaction Steps
Condensation of 3-(2-Chloro-4-fluorophenyl)-1-propylamine (1.5 g, 6.5 mmol) and ketone 5 (1.5 g, 6.5 mmol), following the procedure described in Example 1, gave 6-{trans-4-[3-(2-chloro-4-fluorophenyl)-propylamino]cyclohexyl}-3H-benzoxazol-2-one (535 mg, 21%), as a white solid: 1H NMR (500 MHz, DMSO-d6): δ 7.41-7.35 (m, 2H), 7.17-7.13 (m, 2H), 6.99-6.94 (m, 2H), 3.60-2.90 (br s, 2H), 2.72 (t, J=8 Hz, 2H), 2.59 (t, J=8 Hz, 2H), 2.49-2.40 (m, 2H), 1.95 (br d, J=12 Hz, 2H), 1.77 (br d, J=12 Hz, 2H), 1.69-1.66 (m, 2H), 1.44 (dddd, J=13, 13, 13, 3 Hz, 2H), 1.13 (dddd, J=13, 13, 13, 3 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06794402B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-27d0a3a47da7475f9f0c998164db1698 |
| Source note | uspto-grants-2004_09 |