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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 359034Erstellt: 24. Oktober 2026

Dimethylformamide → 4-[1-(2-chlorophenyl)-1H-indazol-3-yl]-1-piperazine carboxamide

https://huagongshe.com/de/reaction/359034

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktDiisopropyl EtherHCID 7914—
EduktNitroureaHCID 62372—
Edukt1-(2-chlorophenyl)-3-(1-piperazinyl)-1H-indazoleHCID 15117079—
LösungsmittelWaterHCID 962—
Produkt4-[1-(2-chlorophenyl)-1H-indazol-3-yl]-1-piperazine carboxamideHCID 1511710144,5%

Reaktionsschritte

A mixture of 7.9 g of 1-(2-chlorophenyl)-3-(1-piperazinyl)-1H-indazole, 7.3 g of nitrourea and 100 ml of dimethylformamide was heated on a steam bath for 15 minutes. The reaction mixture was diluted with water and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous magnesium sulfate and concentrated. The concentrate was flash chromatographed on silica gel eluting with chloroform/methanol (5%). Concentration of the appropriate fraction yielded a foam, which when stirred overnight with isopropyl ether afforded 4.0 g of 4-[1-(2-chlorophenyl)-1H-indazol-3-yl]-1-piperazine carboxamide as a powder. A 3.4 g sample of the free base was dissolved in diethyl ether and treated with 1.1 g of fumaric acid. The resulting salt was recrystallized from ethyl acetate to yield 2.3 g (22%) of 4-[1-(2-chlorophenyl)-1H-indazol-3-yl]-1-piperazine carboxamide hemifumarate, m.p. 156°-158°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04999356
Quelldatensatzuspto-grants-1991_03
ORD IDord-de53b221082b433690531e16aba7a050
Quellennotizuspto-grants-1991_03