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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276878Generated: October 31, 2026

3-Bromoaniline → HCID 18548976, compound

https://huagongshe.com/reaction/276878

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromoanilineHCID 11562—
ReactantHCID 18548986HCID 18548986—
SolventEthanolHCID 702—
ProductHCID 18548976HCID 18548976—

Reaction Steps

To 626 mg of 4-chloro-6-trimethylsilanylethynyl-[1.7]naphthyridine-3-carbonitrile in 20 mL of absolute ethanol was added 1 mL of 3-bromoaniline. After refluxing the reaction under an inert atmosphere for 18 hours, the reaction mixture was cooled to ambient temperature, concentrated to 5 mL, diluted with ether, and the product filtered and washed with ether. Drying in vacuo yielded 500 mg of 4-(3-bromo-phenylamino)-6-trimethylsilanylethynyl-[1.7]naphthyridine-3-carbonitrile as an off-white solid: melting point 125° C. (sublimed); mass spectrum (m/e): M+H 421.1, 423.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355636B1
Source datasetuspto-grants-2002_03
ORD IDord-8b622c2e0f564ce69b9f90fca3abb364
Source noteuspto-grants-2002_03