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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1737261Erstellt: 25. Oktober 2026

Dichloromethane → 3-Aminopyrazine-2-carboxylic acid 2-chlorophenylamide

https://huagongshe.com/reaction/1737261

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
Edukt2-ChloroanilineHCID 7240—
Edukt3-Amino-2-pyrazinecarboxylic acidHCID 72656—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-Aminopyrazine-2-carboxylic acid 2-chlorophenylamideHCID 5409697250%

Reaktionsschritte

A mixture of 3-aminopyrazine carboxylic acid (7.0 g, 50.32 mmol), methylene chloride (60 mL), dimethylformamide (40 mL), 4-dimethylaminopyridine (15.37 g, 126 mmol), 2-chloroaniline (5.82 mL, 55.35 mmol), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (11.58 g, 60.38 mmol) was stirred overnight at ambient temperature. The solvent was removed and the residue was mixed with ethyl acetate and 1 N lithium chloride. The precipitate which formed was filtered and rinsed with 1 N lithium chloride, ethyl acetate, and ether and then air dried to afford 6.22 g (50%) of 3-aminopyrazine-2-carboxylic acid 2-chlorophenylamide as fluffy yellow crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05962457
Quelldatensatzuspto-grants-1999_10
ORD IDord-a675d8e5dc164ae1863f90a786c27a9a
Quellennotizuspto-grants-1999_10