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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2391868Generated: October 30, 2026

Water → 8-(3,5-Dimethoxy-phenyl)-quinoxaline-5-carboxylic acid [5-(4-ethyl-piperazin-1-ylmethyl)-pyridin-2-yl]-amide

https://huagongshe.com/reaction/2391868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant5-[(4-Ethyl-1-piperazinyl)methyl]-2-pyridinamineHCID 45489910—
Reactant8-(3,5-Dimethoxy-phenyl)-quinoxaline-5-carboxylic acid ethyl esterHCID 66914690—
SolventTolueneHCID 1140—
Product8-(3,5-Dimethoxy-phenyl)-quinoxaline-5-carboxylic acid [5-(4-ethyl-piperazin-1-ylmethyl)-pyridin-2-yl]-amideHCID 5929295835.1%

Reaction Steps

8-(3,5-dimethoxy-phenyl)-quinoxaline-5-carboxylic acid ethyl ester (Step 115.1) (100 mg, 0.30 mmol) and 5-(4-ethyl-piperazin-1-ylmethyl)-pyridin-2-ylamine (Step 26.1; purified by column chromatography) (78 mg, 0.36 mmol, 1.2 equiv) in toluene (2 mL). The reaction mixture was stirred for 1 h at rt, heated to reflux, stirred for 3 h, allowed to cool, poured onto EtOAc and H2O, and filtered through a pad of celite. The filtrate was extracted with EtOAc. The organic phase was washed with H2O and brine, dried (Na2SO4), filtered and concentrated. The residue was purified by silica gel column chromatography (DCM/MeOH/NH3aq, 94:5:1) followed by reverse-phase preparative HPLC to afford 54 mg of the title compound as a pale yellow solid. Title compound: ESI-MS: 513.2 [M+H]+; tR=3.54 min (System 1); TLC: Rf=0.29 (DCM/MeOH/NH3aq, 94:5:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273882B2
Source datasetuspto-grants-2012_09
ORD IDord-0be18bb845464695b3a5935d97996bf3
Source noteuspto-grants-2012_09