HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 86270096, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 86269905 | HCID 86269905 | — |
| Product | HCID 86270096 | HCID 86270096 | — |
Reaction Steps
The title compound was prepared from racemic cis-2-(1-(4-bromobenzyl)-6-((4-chloro-1-methyl-1H-pyrazol-3-yl)methoxy)-1H-benzo[d]imidazol-2-yl)cyclohexanecarboxylic acid using analogous conditions described in Example 152 using piperidine. MS (ESI): mass calcd. for C31H36ClN5O3, 562.12; m/z found, 562.2 [M+H]+. 1H NMR (400 MHz, CD3OD) δ 7.65 (s, 1H), 7.53 (d, J=8.8, 1H), 7.03 (d, J=8.9, 3H), 6.92 (d, J=8.8, 3H), 5.44 (d, J=16.6, 1H), 5.37 (d, J=16.4, 1H), 4.98 (s, 2H), 3.81 (s, 3H), 3.60-3.49 (m, 1H), 3.14-3.09 (m, 4H), 2.91-2.79 (m, 1H), 2.40-2.28 (m, 1H), 2.03-1.93 (m, 1H), 1.91-1.63 (m, 8H), 1.62-1.53 (m, 2H), 1.53-1.37 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952177B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-8765ec7d111a47a58bb4b9cbabedba08 |
| Source note | uspto-grants-2015_02 |