HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methyl-alpha-(4-methylphenyl)benzeneacetic acid → N-{5-[1-(3-{[Bis(4-methylphenyl)acetyl]amino}propyl)4-piperidinyl]-2-fluorophenyl}butanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methyl-alpha-(4-methylphenyl)benzeneacetic acid | HCID 30314 | — |
| Reactant | N-{5-[1-(3-aminopropyl)4-piperidinyl]-2-fluorophenyl}butanamide | HCID 21957132 | — |
| Product | N-{5-[1-(3-{[Bis(4-methylphenyl)acetyl]amino}propyl)4-piperidinyl]-2-fluorophenyl}butanamide | HCID 21957134 | — |
Reaction Steps
Example 10 prepared from bis(4-methylphenyl)acetic acid and N-{5-[1-(3-aminopropyl)-4-piperidinyl]-2-fluorophenyl}butanamide according to the procedures described in Scheme 10: 1H NMR (400 MHz, CDCl3) δ 8.30–8.13 (m, 1H), 8.08–7.92 (br, 1H), 7.43–6.89 (m, 9H), 6.76–6.61 (br, 1H), 4.98–4.79 (br, 1H), 4.70 (s, 1H), 3.39–3.16 (m, 4H), 2.83–2.63 (m, 2H), 2.63–2.47 (m, 1H), 2.45–2.12 (m, 4H), 2.27 (s, 6H), 2.02–1.64 (m, 8H), 1.02 (t, 3H, J=7.2 Hz); ESMS m/e: 544.4 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07199135B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-d86a27bfac1346689e14f4b876cfbb1d |
| Source note | uspto-grants-2007_04 |