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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383236Generated: October 30, 2026

2-Amino-7-chloro-1-ethyl-N-methyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxamide → (+/-)-2-Amino-7-(3,4-dimethoxy-3-methylbut-1-yn-1-yl)-1-ethyl-N-methyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxamide

https://huagongshe.com/reaction/2383236

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-7-chloro-1-ethyl-N-methyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxamideHCID 86642336—
Reactant(+/-)-3,4-Dimethoxy-3-methylbut-1-yneHCID 86642359—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
Solventtriethylamine N,N-dimethylformamideHCID 22056947—
Product(+/-)-2-Amino-7-(3,4-dimethoxy-3-methylbut-1-yn-1-yl)-1-ethyl-N-methyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxamideHCID 25127281—

Reaction Steps

A suspension of 1.5 g (5.34 mmol) of 2-amino-7-chloro-1-ethyl-N-methyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxamide in 30 ml of a DMF/Et3N (v/v; 2/1) mixture is placed in an 80 ml microwave tube. Argon is sparged into this suspension for 10 minutes and then 1.37 g of (±)-3,4-dimethoxy-3-methylbut-1-yne (10.69 mmol), 0.101 g of CuI (0.53 mmol) and 0.187 g of bis(triphenylphosphine)palladium(II) dichloride (0.27 mmol) are successively added.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263614B2
Source datasetuspto-grants-2012_09
ORD IDord-5a9017f61cc5492aab2e2104a92402d2
Source noteuspto-grants-2012_09