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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1667677Erstellt: 27. Oktober 2026

Dimethylformamide → 2-(5-Dimethoxymethyl-2-nitro-phenylamino)-4-phenyl-thiazole-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1667677

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktCesium carbonateHCID 10796—
EduktEthyl 2-amino-4-phenyl-1,3-thiazole-5-carboxylateHCID 73239—
Edukt4-Dimethoxymethyl-2-fluoro-1-nitrobenzeneHCID 54032292—
LösungsmittelWaterHCID 962—
Produkt2-(5-Dimethoxymethyl-2-nitro-phenylamino)-4-phenyl-thiazole-5-carboxylic acid ethyl esterHCID 8664280454,1%

Reaktionsschritte

A mixture of 0.250 g (1 mmole) of 2-amino-4-phenyl-thiazole-5-carboxylic acid ethyl ester (V.1), 0.215 g (1 mmole) of 4-dimethoxymethyl-2-fluoro-1-nitro-benzene, 0.488 g (1.5 mmole) of cesium carbonate and 5 mL of dimethylformamide was heated at 100 degrees overnight. The cooled mixture was diluted with 30 mL of water and then extracted three times with 20 mL of ethyl acetate. The combined organic layers were washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography, eluting with ethyl acetate-hexanes (gradient 0:100-10:90) to give 0.240 g of 2-(5-dimethoxymethyl-2-nitro-phenylamino)-4-phenyl-thiazole-5-carboxylic acid ethyl ester (VIA a) as an orange solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08044213B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-209deecfd88e4b9cae5e5829a02b08b4
Quellennotizuspto-grants-2011_10