HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 136027655, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | HCID 136027649 | HCID 136027649 | — |
| Reactant | HCID 136027653 | HCID 136027653 | — |
| Product | HCID 136027655 | HCID 136027655 | — |
Reaction Steps
The titled compound was prepared in a manner analogous to Example 171, substituting 3-cyanobenzaldehyde for benzaldehyde in step A. Step C yielded a mixture of 1-[6-(3-cyano-benzylamino)-4-oxo-3,4-dihydro-quinazolin-2-yl]-1H-pyrazole-4-carboxylic acid, 1-[6-(3-carbamoyl-benzylamino)-4-oxo-3,4-dihydro-quinazolin-2-yl]-1H-pyrazole-4-carboxylic acid, and the titled compound. The mixture was separated by reverse-phase HPLC; the titled compound was recovered as the trifluoroacetate salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08937078B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-db5be0e064c54471ad39f779c438ad3f |
| Source note | uspto-grants-2015_01 |