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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188267Generated: October 29, 2026

Potassium Carbonate → 1-[4-(3,4-Dichlorophenoxy)-3-methylaminomethyl-phenyl]-1H-pyrazol-3-ylamine dihydrochloride

https://huagongshe.com/reaction/2188267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant[5-Bromo-2-(3,4-dichloro-phenoxy)-benzyl]-methyl-amineHCID 9947009—
ReactantHCID 178418806HCID 178418806—
CatalystCopperHCID 23978—
Product1-[4-(3,4-Dichlorophenoxy)-3-methylaminomethyl-phenyl]-1H-pyrazol-3-ylamine dihydrochlorideHCID 70028753—

Reaction Steps

Under N2 in a flame-dried 15 mL round bottomed flask, fitted with a magnetic stirrer were placed 318 mg (0.88 mmol) of 5-bromo-2-(3,4-dichlorophenoxy)-N-methylbenzylamine (title compound of Example 15), 1.50 g (18 mmol) of 3-aminopyrazole, 56 mg (0.88 mmol) of copper powder and 122 mg (0.88 mmol) of potassium carbonate. The mixture was heated to 130° C. for a total of one hour, cooled and stirred at room temperature overnight. The tarry residue was partitioned between EtOAc and dilute aqueous EDTA (ethylenediaminetetraacetic acid), the organic layer was washed with water and saturated aqueous NaCl, then dried over Na2SO4. After filtration the solvent was removed in vacuo to give an oil, 287 mg, which was eluted on silica gel with a gradient system of NH4OH:CH3OH:CHCl3 (from 2:2:96 to 2:10:88). The product fractions were concentrated to an oil (110 mg) which was dissolved in 25 mL EtOAc and treated with 0.6 mL of 1 N HCl in Et2O. The solids which precipitated were filtered, washed with a small amount of Et2O and dried under vacuum to give 60 mg of the title product, m.p. 225-233° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410736B1
Source datasetuspto-grants-2002_06
ORD IDord-3d5703e56f62443cbefc108b8b9bedca
Source noteuspto-grants-2002_06