HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bis(4-chlorophenyl)acetic acid → N-{3-[1-(3-{[2,2-bis(4-chlorophenyl)acetyl]amino}propyl)-4-piperidinyl]phenyl}butanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bis(4-chlorophenyl)acetic acid | HCID 6730 | — |
| Reactant | N-{3-[1-(3-aminopropyl)-4-piperidinyl]phenyl}butanamide | HCID 21957120 | — |
| Product | N-{3-[1-(3-{[2,2-bis(4-chlorophenyl)acetyl]amino}propyl)-4-piperidinyl]phenyl}butanamide | HCID 21957203 | — |
Reaction Steps
Example 53 was prepared from bis(4-chlorophenyl)acetic acid and N-{3-[1-(3-aminopropyl)-4-piperidinyl]phenyl}butanamide according to the procedures described in Scheme 10: 1H NMR (400 MHz, CDCl3) δ 7.67 (s, 1H), 7.58 (s, 1H), 7.49 (br s, 1H), 7.28–7.21 (m, 10H), 6.91 (m, 1H), 4.77 (s, 1H), 3.38 (dd, 2H, J=6.0, 11.6 Hz), 2.93 (d, 2H, J=11.6 Hz), 2.46 (m, 1H), 2.41 (t, 2H, J=6.0 Hz), 2.31 (t, 2H, J=7.2 Hz), 1.96 (dt, 2H, J=1.6, 12.0 Hz); 1.82–1.66 (m, 6H), 1.58–1.54 (m, 2H), 0.98 (t, 3H, J=7.6 Hz); ESMS m/e: 566.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07199135B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-d8cc724dbe7244938756b066444bbe0e |
| Source note | uspto-grants-2007_04 |