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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1093703Erstellt: 26. Oktober 2026

Water → N-(5-phenyl-thiazol-2-yl)-malonamic acid ethyl ester

https://huagongshe.com/reaction/1093703

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktDiisopropylethylamineHCID 81531—
Edukt5-Phenyl-thiazol-2-ylamineHCID 873119—
Edukt2-Ethylpropanedioyl dichlorideHCID 10920924—
LösungsmittelChloroformHCID 6212—
ProduktN-(5-phenyl-thiazol-2-yl)-malonamic acid ethyl esterHCID 8663462646%

Reaktionsschritte

To a stirred solution of 5-phenyl-thiazol-2-ylamine (0.4 g, 0.0022 mol) and DIEA (0.73 g, 0.0056 mol) in chloroform (4 mL) was added mono-ethylmalonyl chloride (0.375 g, 0.0024 mol) dropwise at 0° C. and the resulting mixture was stirred at ambient temperature for 20 minutes. The reaction mixture was then diluted with cold water and the product was extracted with chloroform. The chloroform was washed with saturated sodium bicarbonate solution and brine, dried over Na2SO4 and evaporated under reduced pressure to afford 0.3 g (46%) of N-(5-phenyl-thiazol-2-yl)-malonamic acid ethyl ester. To a solution of N-(5-phenyl-thiazol-2-yl)-malonamic acid ethyl ester (0.292 g, 0.001 mol) in the mixture of methanol (1 mL), THF (1.5 mL) and H2O (1 mL) was added LiOH.H2O (0.084 g, 0.002 mol) and the resulting mixture was stirred for 1 hour. The reaction mixture was then concentrated. The residue was diluted with water, acidified with concentrated HCl and the product was extracted with ethylacetate. The ethyl acetate was washed with brine, dried over Na2SO4 and evaporated under reduced pressure to afford 0.23 g (87%) of N-(5-phenyl-thiazol-2-yl)-malonamic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08129376B2
Quelldatensatzuspto-grants-2012_03
ORD IDord-345944743ff6446d9be01f6163afce3a
Quellennotizuspto-grants-2012_03