HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 178517788, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 178517787 | HCID 178517787 | — |
| Product | HCID 178517788 | HCID 178517788 | — |
Reaction Steps
The title compound was prepared from 7-chloro-4-hydroxy-2-trifluoromethylquinazoline (2.0 g, 8.0 mmol), as described in Example 43 (but using piperidine in place of N,N-dimethylamine) to provide the desired compound in a 96% (2.5 g) yield; m.p. 268-271° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06150372 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-60143bc82bbb44519f22f31dc314f317 |
| Source note | uspto-grants-2000_11 |