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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807388Generated: October 30, 2026

Triethylamine → HCID 131730168, compound

https://huagongshe.com/reaction/1807388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-(Difluoromethyl)-1-methyl-1 H-pyrazole-4-carbonyl chlorideHCID 15340110—
ReactantHCID 86669069HCID 86669069—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 131730168HCID 131730168100%

Reaction Steps

To a stirred solution of trans N-{1-[2-(2-Chloro-6-fluoro-phenyl)-cyclopropyl]-ethyl}-O-methyl-hydroxylamine (0.80 g; 3.3 mmol) prepared as described in example P14 and triethylamine (0.60 ml; 4.3 mmol) in dichloromethane (10 ml) at ambient temperature was added dropwise 3-difluoromethyl-1-methyl-1H-pyrazole-4-carbonyl chloride (0.64 g; 3.3 mmol). The reaction mixture was stirred for 16 hours at ambient temperature then poured in water (60 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 1.30 g (100% of theory) of trans 3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxylic acid {1-[2-(2-chloro-6-fluoro-phenyl)-cyclopropyl]-ethyl}-methoxy-amide as a clear viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357635B2
Source datasetuspto-grants-2013_01
ORD IDord-e44febccd02245e7ae3a760b4d057c9e
Source noteuspto-grants-2013_01