HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(4-Phenylpiperidin-4-yl)acetamide → HCID 21839969, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(4-Phenylpiperidin-4-yl)acetamide | HCID 15886675 | — |
| Reactant | HCID 21839905 | HCID 21839905 | — |
| Product | HCID 21839969 | HCID 21839969 | 101.5% |
Reaction Steps
3-(3,4-Dichlorophenyl)-3-(6-hydroxy-2-methyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)propionaldehyde (1.5 g) was coupled to 4-acetamido-4-phenylpiperidine (0.7 g) by a method similar to that described in Example 8. The reaction product was purified by chromatography and converted to the corresponding hydrochloride salt as described in Example 8 to afford the title compound (1.26 g); mp 212°-225° C.; MS: m/z=566(m+1); NMR: 2.00 (s,3), 2.22(m,5), 2.5 (m,2), 2.7(m,2), 2.99(s,3), 3.54(m, 1), 4.54 (d,1, J=3.4), 5.81 (s,1), 6.6 (m,1), 6.7 (m, 1), 6.97 (m, 1), 7.11 (m,2), 7.31 (m,6), 7.50 (d,1, J=8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05589489 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-517accef64ea4628803cc9df2ec5816a |
| Source note | uspto-grants-1996_12 |