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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289913Generated: October 29, 2026

Acetic Anhydride → 7-(Acetylamino)-N-[(4-chlorophenyl)methyl]-4-hydroxy-3-quinolinecarboxamide

https://huagongshe.com/reaction/2289913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178507324HCID 178507324—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
Product7-(Acetylamino)-N-[(4-chlorophenyl)methyl]-4-hydroxy-3-quinolinecarboxamideHCID 178474046—

Reaction Steps

A solution of 100 mg of 7-amino-N-[(4-chlorophenyl)methyl]-4-hydroxy-3-quinolinecarboxamide in 1 mL of anhydrous pyridine is treated with 0.032 mL of acetic anhydride. After 24 h, an additional 0.005 mL of acetic anhydride is added and the mixture is stirred for an additonal 48 h. The mixture is diluted with 2 mL of distilled water and the precipitate is collected by filtration. It is washed with two 1 mL portions of distilled water and dried in a stream of air. It is dried at 20 torr/75°C./16 h. The product is obtained as 78 mg of a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093732
Source datasetuspto-grants-2000_07
ORD IDord-c4d215c891264b4ebdaf88de5835b42d
Source noteuspto-grants-2000_07