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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428883Generated: October 30, 2026

Benzaldehyde → HCID 136027655, compound

https://huagongshe.com/reaction/1428883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHCID 136027649HCID 136027649—
ReactantHCID 136027653HCID 136027653—
ProductHCID 136027655HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937078B2
Source datasetuspto-grants-2015_01
ORD IDord-db5be0e064c54471ad39f779c438ad3f
Source noteuspto-grants-2015_01