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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415518Generated: October 30, 2026

4-Chlorobutyryl chloride → HCID 66620109, compound

https://huagongshe.com/reaction/415518

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobutyryl chlorideHCID 78370—
Reactant4-Chloro-1,5-naphthyridin-3-amineHCID 66619961—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 66620109HCID 66620109—

Reaction Steps

A mixture of 4-chloro[1,5]naphthyridin-3-amine (2.0 g, 11 mmol) and 4-chlorobutyryl chloride (4.7 g, 33 mmol) in 1,2-dichloroethane (75 mL) was heated at reflux for 20 hours. The reaction mixture was then concentrated under reduced pressure and the residue washed with two 25 mL portions of hexane. The solid was then taken up in methanol (35 mL), 1.0 mL of 10% solution of sodium hydroxide in water was added, and the solution was stirred at room temperature for 4 hours. The reaction mixture was then concentrated under reduced pressure to provide 4-chloro-N-(4-chloro[1,5]naphthyridin-3-yl)butanamide which was used directly in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088788B2
Source datasetuspto-grants-2012_01
ORD IDord-5f1d9f5421b444c0a23c14a28b7ac1db
Source noteuspto-grants-2012_01