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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19494Erstellt: 24. Oktober 2026

Methanesulfonic Acid → N-[3-(1H-Imidazol-2-ylamino)-4-methyl-phenyl]-3-trifluoromethyl-benzamide

https://huagongshe.com/de/reaction/19494

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanesulfonic AcidHCID 6395—
Eduktm-(Trifluoromethyl)benzamideHCID 74535—
EduktN-(2,2-diethoxyethyl)carbodiimideHCID 10749464—
LösungsmittelEthanolHCID 702—
ProduktN-[3-(1H-Imidazol-2-ylamino)-4-methyl-phenyl]-3-trifluoromethyl-benzamideHCID 58973096—

Reaktionsschritte

A mixture of N-(2,2-diethoxyethyl)carbodiimide (398 mg, 2.51 mmol), 3-amino-4-methyl-phenyl]-3-trifluoromethyl-benzamide (649 mg, 2.20 mmol), methanesulfonic acid (143 μL, 2.20 mmol) in ethanol (25 mL) is heated at reflux for 16 hours. An additional portion of N-(2,2-diethoxyethyl)carbodiimide (525 mg, 3.32 mmol) and methanesulfonic acid (143 μL, 2.20 mmol) are added. After an additional 3 hours refluxing, the reaction mixture is concentrated. The residue is dissolved in HCl (6N, 5 mL) and ethanol (5 mL). After stirring overnight, the reaction mixture is concentrated and basified with 25% NaOH solution to a pH of 14. The mixture is stirred for 30 minutes, extracted with CH2Cl2, dried, concentrated and purified by column chromatography (silica gel, eluting with 7N NH3 in methanol:dichloromethane from 2% to 4%) to give the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745437B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-2b6863eb1d6b4541a5678bf5343bed44
Quellennotizuspto-grants-2010_06