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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308598Generated: November 3, 2026

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

https://huagongshe.com/reaction/2308598

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 numberUS04690924
Source datasetuspto-grants-1987_09
ORD IDord-fe7adc4bc403478bb208bcdc40a80602
Source noteuspto-grants-1987_09