HuagongsheHuagongshe Chemistry Print Report · For research reference only
[3-(Trifluoromethyl)-1-trityl-1H-pyrazol-4-YL]boronic acid → 1-[6-(3-trifluoromethyl-1-trityl-1H-pyrazol-4-yl)quinolin-4-yl]-piperidine-4-carboxylic acid (4-fluorophenyl)methylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | [3-(Trifluoromethyl)-1-trityl-1H-pyrazol-4-YL]boronic acid | HCID 22032227 | — |
| Reactant | 1-(6-Bromoquinolin-4-yl)piperidine-4-carboxylic acid (4-fluorophenyl)methylamide | HCID 86760173 | — |
| Product | 1-[6-(3-trifluoromethyl-1-trityl-1H-pyrazol-4-yl)quinolin-4-yl]-piperidine-4-carboxylic acid (4-fluorophenyl)methylamide | HCID 86760172 | 90.3% |
Reaction Steps
92 mg 1-(6-bromoquinolin-4-yl)piperidine-4-carboxylic acid (4-fluorophenyl)methylamide (compound in Production Example 458) and 114 mg 3-trifluoromethyl-1-trityl-1H-4-pyrazolylboronic acid (compound in Production Example 31) were reacted in the same manner as in Example 9, to give 139 mg 1-[6-(3-trifluoromethyl-1-trityl-1H-pyrazol-4-yl)quinolin-4-yl]-piperidine-4-carboxylic acid (4-fluorophenyl)methylamide. This product was reacted in the same manner as in Example 67, to give 80 mg of the title compound as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07074801B1 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-4c33bc0b97a8476287958cb5a2f4d6df |
| Source note | uspto-grants-2006_07 |