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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 244722Erstellt: 23. Oktober 2026

Triethylamine → 4-Chloro-N-[6-(1H-indol-4-yl)-1H-indazol-4-yl]-1-methyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/de/reaction/244722

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-Chloro-N,N-2-trimethylpropenylamineHCID 640792—
Edukt4-chloro-1-methyl-1H-pyrazole-5-carboxylic acidHCID 670823—
Edukt6-(1H-indol-4-yl)-1H-indazol-4-amineHCID 58268019—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Chloro-N-[6-(1H-indol-4-yl)-1H-indazol-4-yl]-1-methyl-1H-pyrazole-5-carboxamideHCID 4454098112,4%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

A solution of 4-chloro-1-methyl-1H-pyrazole-5-carboxylic acid (available from Fluorochem) (50 mg) in dry DCM (10 ml) was treated with 1-chloro-N,N,2-trimethyl-1-propen-1-amine (0.041 ml) (available from Acros) and allowed to stir at 20° C. for 10 min when a solution of 6-(1H-indol-4-yl)-1H-indazol-4-amine (77 mg) and triethylamine (0.043 ml) in DCM (5 ml) was added and the mixture stirred at 20° C. for 18 h. The mixture was poured onto an aminopropyl SPE cartridge (1 g) and allowed to stand for 2 h, then the mixture was eluted with methanol (5 ml) and blown to dryness under a stream of nitrogen. The crude product was purified by mass directed preparative HPLC (Method A) to give the title compound as a white solid (15 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658635B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-2b1ae7de5fd848489294a21c25a2a9c3
Quellennotizuspto-grants-2014_02