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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202523Generated: October 26, 2026

Ethyl Acetate → 3-Amino-6-(2,4-dichloro-phenyl)-5-trifluoromethyl-pyridine-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/2202523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(2,4-Dichlorophenyl)boronic acidHCID 2734659—
ReactantMethyl 3-amino-6-bromo-5-(trifluoromethyl)picolinateHCID 58964428—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product3-Amino-6-(2,4-dichloro-phenyl)-5-trifluoromethyl-pyridine-2-carboxylic acid methyl esterHCID 67383408—

Reaction Conditions

Temperature110 °C

Reaction Steps

3-Amino-6-bromo-5-trifluoromethyl-pyridine-2-carboxylic acid methyl ester (Intermediate A4) (3 g, 10.03 mmol), 2,4-dichlorophenylboronic acid (2.297 g, 12.04 mmol), potassium phosphate (4.26 g, 20.06 mmol) and Fibrecat® 1034A (Johnson Matthey, polymer supported palladium complex) (500 mg, 10.03 mmol) were suspended in toluene (50 ml) and water (15 ml). The reaction mixture was heated to 110° C. under vigorous stirring for 3 hours. The mixture was allowed to cool to RT and EtOAc (100 ml) was added. The organic layer was separated and washed with brine (15 ml). MP-TMT (macroporous polystyrene-bound trimercaptotriazine, 3 g, Polymern labs) was added and stirred for 1 hour at RT. MgSO4 was added and the suspension filtered off. The filtrate was concentrated in vacuo and purification of the residue by reverse phase chromatography (130 g C18 column) eluting with water/MeOH afforded the title compound as a white solid; LS-MS Rt=1.55 mins [M+H]+ 365 (Method 2minLC_v002).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365552B2
Source datasetuspto-grants-2016_06
ORD IDord-3b50c2e4826d4db090cba481279e1327
Source noteuspto-grants-2016_06