HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2-Diphenylacetyl chloride → HCID 21957147, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2-Diphenylacetyl chloride | HCID 74637 | — |
| Reactant | N-{3-[1-(3-aminopropyl)4-piperidinyl]phenyl}cyclopropanecarboxamide | HCID 21957166 | — |
| Product | HCID 21957147 | HCID 21957147 | — |
Reaction Steps
Example 17 was prepared from diphenylacetyl chloride and N-{3-[1-(3-aminopropyl)-4-piperidinyl]phenyl}cyclopropanecarboxamide according to the procedures described in Scheme 8: 1H NMR (400 MHz, CDCl3) δ 9.26–9.09 (br, 1H), 8.12–7.91 (br, 1H), 7.69 (d, 1H, J=7.2 Hz), 7.63–7.42 (br, 1H), 7.43–7.12 (m, 11H), 6.88 (d, 1H, J=7.2 Hz), 5.03 (s, 1H), 3.53–3.27 (m, 4H), 2.99–2.84 (m, 2H), 2.84–2.58 (m, 3H), 2.40–2.16 (m, 2H), 2.16–1.98 (m, 2H), 1.98–1.83 (m, 2H), 1.78–1.64 (m, 1H), 1.10–0.97 (m, 2H), 0.90–0.76 (m, 2H); ESMS m/e: 496.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105544B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-1c982131f2cd4e4da6a4798052fbba97 |
| Source note | uspto-grants-2006_09 |