HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(p-Chlorophenyl)cyclobutanecarboxylic acid → HCID 21957244, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(p-Chlorophenyl)cyclobutanecarboxylic acid | HCID 602761 | — |
| Reactant | N-{3-[1-(3-aminopropyl)-4-piperidinyl]phenyl}2-methylpropanamide | HCID 16757470 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21957244 | HCID 21957244 | — |
Reaction Steps
Example 43 was prepared from 1-(4-chlorophenyl)cyclobutanecarboxylic acid and N-{3-[1-(3-aminopropyl)-4-piperidinyl]phenyl}-2-methylpropanamide according to the procedures described in Scheme 9: 1H NMR (400 MHz, CDCl3) δ 7.56 (s, 1H), 7.41 (s, 1H), 7.34–7.21 (m, 6H), 6.93 (s, 1H), 6.48 (s, 1H), 3.31–3.24 (m, 2H), 2.94–2.86 (m, 2H), 2.86–2.76 (m, 2H), 2.57–2.37 (m, 4H), 2.33–2.26 (m, 2H), 2.12–2.02 (m, 1H), 1.97–1.87 (m, 3H), 1.82 (s, 1H), 1.79 (s, 1H), 1.70–1.56 (m, 4H), 1.24 (d, 6H, J=7.2 Hz); ESMS m/e: 496.3 (M+H)+; Anal. Calc. for C29H38ClN3O2.0.550 CHCl3: C, 63.18; H, 6.92; N, 7.48. Found: C, 63.22; H, 6.90; N, 7.48.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07199135B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-61e64a4a725b4e719922607efc341ec7 |
| Source note | uspto-grants-2007_04 |