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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1748611Erstellt: 26. Oktober 2026

Triethylamine → N-(6-Bromo-2-methylpyridin-3-yl)-5-methyl-1-[5-(trifluoromethyl)pyridin-2-yl]-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/1748611

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt6-Bromo-2-methylpyridin-3-amineHCID 14418045—
Edukt5-methyl-1-[5-(trifluoromethyl)pyridin-2-yl]-1H-pyrazole-4-carboxylic acid chlorideHCID 89734997—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-(6-Bromo-2-methylpyridin-3-yl)-5-methyl-1-[5-(trifluoromethyl)pyridin-2-yl]-1H-pyrazole-4-carboxamideHCID 86692559100,6%

Reaktionsschritte

To a solution of 5-amino-2-bromo-6-picoline (701 mg) and triethylamine (1.57 ml) in tetrahydrofuran (20 ml) was added 5-methyl-1-[5-(trifluoromethyl)pyridin-2-yl]-1H-pyrazole-4-carboxylic acid chloride (1.34 g) described in Reference Example 180 under ice-cooling, and stirred at room temperature for 1.5 hours. After completion of the reaction, the solvent was evaporated, and saturated sodium bicarbonate water was added thereto. The insoluble matter was collected by filtration, washed with water, and then dried in vacuo to give the titled compound as a pale yellow solid (1.66 g). MS (ESI) m/z: 440 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09150555B2
Quelldatensatzuspto-grants-2015_10
ORD IDord-ee3c100f965d4379ae4ccacad9c42476
Quellennotizuspto-grants-2015_10