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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057332Generated: October 27, 2026

7-Benzyloxy-4-chloro-6-methoxycinnoline hydrochloride → 4-Chloro-7-hydroxy-6-methoxycinnoline

https://huagongshe.com/reaction/1057332

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Benzyloxy-4-chloro-6-methoxycinnoline hydrochlorideHCID 21991007—
SolventTrifluoroacetic acidHCID 6422—
Product4-Chloro-7-hydroxy-6-methoxycinnolineHCID 13575252394%

Reaction Steps

The starting material, 4-chloro-7-hydroxy-6-methoxycinnoline was obtained by heating a solution of 7-benzyloxy-4-chloro-6-methoxycinnoline hydrochloride (3.06 g, 9 mmol), (prepared as described for the starting material in Example 6), in TFA (30 ml) at reflux for 5 hours. After evaporation of the solvent, the residue was suspended in water and adjusted to pH7 with saturated aqueous sodium hydrogen carbonate solution. The resulting solid was filtered off, washed with water and ether and dried under vacuum to give 4-chloro-7-hydroxy-6-methoxycinnoline as a yellow solid (1.78 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06514971B1
Source datasetuspto-grants-2003_02
ORD IDord-7a2a5ada340e43df8378062cf1a3e475
Source noteuspto-grants-2003_02