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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 238368Erstellt: 24. Oktober 2026

4-(Trifluoromethyl)aniline → 1-methyl-N-[4-(trifluoromethyl)phenyl]-1H-pyrazole-5-carboxamide

https://huagongshe.com/de/reaction/238368

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(Trifluoromethyl)anilineHCID 9964—
Edukt1-methyl-1H-pyrazole-5-carboxylic acidHCID 643158—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Edukt1-Hydroxybenzotriazole hydrateHCID 2796029—
LösungsmittelChloroformHCID 6212—
Produkt1-methyl-N-[4-(trifluoromethyl)phenyl]-1H-pyrazole-5-carboxamideHCID 150991247,1%

Reaktionsschritte

A mixture of 1-methyl-1H-pyrazol-5-carboxylic acid (1.00 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.82 g), 1-hydroxybenzotriazole monohydrate (1.70 g) and chloroform (20 mL) was stirred at a room temperature for 15 minutes. Thereafter, 4-aminobenzotrifluoride (1.27 g) was added to the reaction solution, and the obtained mixture was then stirred for 24 hours. Thereafter, the reaction solution was concentrated under a reduced pressure, and the residue was then purified by column chromatography (chromatorex NH, hexane:ethyl acetate=4:1), so as to obtain the title compound (1.00 g) in the form of a colorless solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642626B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-29142283cdf14f43877ba3074fcfb03b
Quellennotizuspto-grants-2014_02