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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352763Generated: November 2, 2026

Hydrochloric Acid → HCID 22025904, compound

https://huagongshe.com/reaction/1352763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant3-Chloro-4-methoxybenzylamineHCID 738038—
CatalystCopper bromide (CuBr2)HCID 24611—
SolventEthyl AcetateHCID 8857—
ProductHCID 22025904HCID 22025904—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of the compound (prepared in the above (1)) 500 mg, 3-chloro-4-methoxybenzylamine 638 mg, potassium carbonate 817 mg, copper bromide 313 mg and 1-methyl-2-pyrrolidinone 10 ml is stirred at 120° C. for 2.5 hours. After cooling to room temperature thereto are added ethyl acetate and 1N hydrochloric acid. The organic layer is separated, washed with water (twice) and brine, and dried over sodium sulfate. After removal of sodium sulfate, the filtrate is concentrated in vacuo, and the residue is purified with column chromatography (silica gel 30 g, solvent; chloroform→chloroform:methanol=70:1) to give 2-(3-chloro-4-methoxybenzylamino)-6-chloronicotinic acid as colorless crystals, 471 mg. mp 184–185.5° C., MS(m/z): 325(M−H)−

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220736B2
Source datasetuspto-grants-2007_05
ORD IDord-09d0be00b8fe4e288e598794e6d6343a
Source noteuspto-grants-2007_05