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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865891Generated: November 2, 2026

Diisopropylethylamine → 6-(4-Chloro-phenyl)-5-(2-methoxy-ethoxy)-pyrazine-2-carboxylic acid (1-hydroxymethyl-cyclopropyl)-amide

https://huagongshe.com/reaction/1865891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Chloro-N,N-2-trimethylpropenylamineHCID 640792—
Reactant(1-Aminocyclopropyl)methanol hydrochlorideHCID 14146222—
Reactant6-(4-Chloro-phenyl)-5-(2-methoxy-ethoxy)-pyrazine-2-carboxylic acidHCID 68799009—
SolventDichloromethaneHCID 6344—
Product6-(4-Chloro-phenyl)-5-(2-methoxy-ethoxy)-pyrazine-2-carboxylic acid (1-hydroxymethyl-cyclopropyl)-amideHCID 6884147957.9%

Reaction Steps

To a suspension of 0.05 g (0.00016 mol) of 6-(4-chloro-phenyl)-5-(2-methoxy-ethoxy)-pyrazine-2-carboxylic acid in 2.0 ml dichloromethane was added 0.024 g 1-chloro-N,N,2-trimethyl-1-propenylamine and the mixture was stirred at room temperature for 30 min. To the resulting slightly brown solution was added 0.040 g of (1-amino-cyclopropyl)-methanol hydrochloride and dropwise 0.1 ml N-ethyldiisopropyl-amine. The mixture was stirred at ambient temperature for 30 min. The resulting mixture was partitioned between 10% aqueous citric acid and ethyl acetate. The phases were separated and the organic phase was dried over magnesium sulfate and evaporated. The residue was purified by chromatography on silica gel using a gradient of heptane to ethyl acetate to yield 0.035 g (55% yield) of the title compound as off white solid. MS (ISP) (M+H+)=378.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629346B2
Source datasetuspto-grants-2009_12
ORD IDord-acf34f4754b84ff58a0652fe8015bbd0
Source noteuspto-grants-2009_12