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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36802Erstellt: 23. Oktober 2026

Ethyl 3-amino-4,4,4-trifluorocrotonate → 3-(4-chloro-5-ethylsulfonylamino-2-fluorophenyl)-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione

https://huagongshe.com/de/reaction/36802

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 3-amino-4,4,4-trifluorocrotonateHCID 5702529—
EduktEthyl 4-chloro-5-ethylsulfonylamino-2-fluorocarbanilateHCID 10903456—
EduktSodium MethoxideHCID 10942334—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(4-chloro-5-ethylsulfonylamino-2-fluorophenyl)-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedioneHCID 1111247977%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

1.06 g (5.77 mmol) of ethyl 3-amino-4,4,4-trifluorocrotonate was dissolved in 6.2 ml of N,N-dimethylformamide and 0.82 g (14.4 mmol) of sodium methoxide was added thereto. The reaction mixture was cooled to not higher than 5° C. after 10 minutes, and 1.56 g (4.81 mmol) of ethyl 4-chloro-5-ethylsulfonylamino-2-fluorocarbanilate was added thereto. The resultant mixture was heated to 110° C. and reacted for 4 hours. After the reaction was completed, N,N-dimethylformamide was distilled off and the resultant product was dissolved in water. The thus-obtained solution was washed with diethyl ether 3 times and thereafter concentrated hydrochloric acid was added thereto to pH 2. The precipitated crystals were filtered out, washed with water and dried to obtain 1.54 g of the objective product (yield: 77%) in the form of light yellow crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05416236
Quelldatensatzuspto-grants-1995_05
ORD IDord-dbd92c8c458a4f7abe5413cf41b0ee55
Quellennotizuspto-grants-1995_05