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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046803Generated: November 1, 2026

Benzaldehyde → HCID 178422688, compound

https://huagongshe.com/reaction/1046803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHCID 59139203HCID 59139203—
SolventMethanolHCID 887—
ProductHCID 178422688HCID 178422688—

Reaction Steps

Methanol (4.0 mL) was added to 3-(3-amino-2-fluorobenzyl)-4-methyl-7-(thiazol-2-yloxy)-2-oxo-2H-1-benzopyran (compound 1h-3-4) (200 mg), and benzaldehyde (0.053 mL) was added to the resultant suspension while stirring at room temperature. The suspension was heated under reflux for 3 hours. The reaction solution was then cooled to room temperature, and the solvent was distilled away under reduced pressure. The resultant residue was purified by silica gel chromatography (amino gel) (dichloromethane) to yield the title compound (233 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569378B2
Source datasetuspto-grants-2013_10
ORD IDord-17f732fe2dc6496a8045cb1fec2eafa5
Source noteuspto-grants-2013_10