Triethylamine → HCID 131730167, compound

Participants

Reaction Steps

To a stirred solution of trans N-{1-[2-(2-chloro-phenyl)-cyclopropyl]-ethyl}-O-methyl-hydroxylamine (0.30 g; 1.3 mmol) prepared as described in example P12 and triethylamine (0.25 ml; 1.7 mmol) in dichloromethane (5.0 ml) at ambient temperature was added dropwise 3-difluoromethyl-1-methyl-1H-pyrazole-4-carbonyl chloride (0.28 g; 1.3 mmol). The reaction mixture was stirred for 16 hours at ambient temperature then poured in water (50 ml) and extracted with dichloromethane (3×25 ml). Combined organic layers were washed with water (10 ml), brine and dried over anhydrous sodium sulphate. The solvent was removed in vacuo and the residue was purified by flash chromatography over silica gel (elution gradient: cyclohexane/ethyl acetate 99:1 to 1:99) to afford 0.46 g (92% of theory) of trans 3-Difluoromethyl-1-methyl-1H-pyrazole-4-carboxylic acid {1-[2-(2-chloro-phenyl)-cyclopropyl]-ethyl}-methoxy-amide as single diastereomere A in form of a clear viscous oil.

Provenance & Evidence