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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 378282Erstellt: 25. Oktober 2026

4,6-Dichloro-2-(pyrrolidin-1-yl)pyrimidine → N-[4-(6-chloro-2-pyrrolidin-1-yl-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamide

https://huagongshe.com/reaction/378282

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4,6-Dichloro-2-(pyrrolidin-1-yl)pyrimidineHCID 19353553—
EduktN-(4-sulfamoyl-phenyl)-acetamide potassium saltHCID 70262342—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktN-[4-(6-chloro-2-pyrrolidin-1-yl-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamideHCID 1064441466%

Reaktionsschritte

0.58 g (0.00266 mol) of 4,6-dichloro-2-pyrrolidin-1-yl-pyrimidine and 1.36 g (0.00539 mol) of N-(4-sulfamoyl-phenyl)-acetamide potassium salt were stirred in 10 ml of 1-methyl-2-pyrrolidone at 140° C. for 8 hours. Then, the solvent was distilled off in a high vacuum, the residue was partitioned in ethyl acetate/water and extracted. The aqueous phase was made acid with 4N HCl and extracted with ethyl acetate. Both organic phases were combined and concentrated. The residue was recrystallized from a small amount of ethanol and the mother liquor was chromatographed over silica gel with cyclohexane/ethyl acetate 2:1 as the eluent. There was obtained a total of 0.62 g (66%) of N-[4-(6-chloro-2-pyrrolidin-1-yl-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamide as whitish crystals; m.p. 229-233° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06030976
Quelldatensatzuspto-grants-2000_02
ORD IDord-61b2fa2185554870b63b78aad13ef317
Quellennotizuspto-grants-2000_02