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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542713Generated: October 26, 2026

Acetic Anhydride → 6-Acetamido-8-bromo-1,7-naphthyridine

https://huagongshe.com/reaction/542713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant8-Bromo-1,7-naphthyridin-6-amineHCID 10704335—
SolventPyridineHCID 1049—
Product6-Acetamido-8-bromo-1,7-naphthyridineHCID 13826732—

Reaction Steps

Suspended in 32 ml of pyridine was 4.84 g of 6-amino-8-bromo-1,7-naphthyridine, followed by an addition of 66 ml of acetic anhydride. The resultant mixture was stirred at room temperature for 4 hours. After the reaction, the reaction mixture was poured in 500 ml of ice water and crystals, which precipitated out, were collected by filtration and then washed thoroughly with water. They were recrystallized from methanol to obtain 5.37 g of 6-acetamido-8-bromo-1,7-naphthyridine as colorless needle-like crystals (yield: 93.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04659710
Source datasetuspto-grants-1987_04
ORD IDord-44421d17edfe4323b8b4172b6c1cf6ce
Source noteuspto-grants-1987_04