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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808507Generated: November 2, 2026

6-(benzyloxy)-7-methoxy-2-(3-nitrophenyl)quinazolin-4(3H)-one → HCID 136078808, compound

https://huagongshe.com/reaction/1808507

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(benzyloxy)-7-methoxy-2-(3-nitrophenyl)quinazolin-4(3H)-oneHCID 136203246—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 136078808HCID 13607880896%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a suspension of 6-(benzyloxy)-7-methoxy-2-(3-nitrophenyl)quinazolin-4(3H)-one (3.21 g, 7.95 mmol) in trifluoroacetic acid (45 mL) was heated at 75±5° C. for 2.5 h. The volatiles were removed in vacuo and residue was taken up with sat. NaHCO3 solution. A light yellow colored solid separated out, which was collected via filtration. The solid was washed with water and dried under vacuum to give 6-hydroxy-7-methoxy-2-(3-nitrophenyl)quinazolin-4(3H)-one (2.38 g, 7.60 mmol, 96%). HPLC retention time 5.486 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357693B2
Source datasetuspto-grants-2013_01
ORD IDord-d01f5832e58242a5b6e4e275ecb0365f
Source noteuspto-grants-2013_01