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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244060Generated: October 27, 2026

Potassium Carbonate → Methyl 2'-[3-[(4-methoxybenzyl)oxy]-4-chlorophenyl]-3,5-dichloro-2,3'-bipyridine-6'-carboxylate

https://huagongshe.com/reaction/244060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-3,5-dichloropyridineHCID 817090—
ReactantWater 1,2-dimethoxyethaneHCID 18180031—
ReactantMethyl 6-[3-[(4-methoxybenzyl)oxy]-4-chlorophenyl]-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-2-carboxylateHCID 66841210—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2'-[3-[(4-methoxybenzyl)oxy]-4-chlorophenyl]-3,5-dichloro-2,3'-bipyridine-6'-carboxylateHCID 6684121638.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 1 g (1.96 mmol) of methyl 6-[3-[(4-methoxybenzyl)oxy]-4-chlorophenyl]-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-2-carboxylate and 0.58 g (2.55 mmol) of 2-bromo-3,5-dichloropyridine in 10 mL of a 2/1 DME/water mixture, argon is sparged through for 10 minutes, followed by successive addition of 0.81 g (5.88 mmol) of K2CO3 and 0.159 g (0.14 mmol) of Pd(PPh3)4. The reaction mixture is heated for 4 hours at 80° C. and then cooled and diluted in 50 mL of EtOAc. The organic phase is washed with 2×20 mL of water, dried over Na2SO4 and then concentrated under reduced pressure. The residue is then purified on a column of silica gel, eluting with a cyclohexane/EtOAc gradient of from 0 to 40% EtOAc, to give 0.4 g of methyl 2′-[3-[(4-methoxybenzyl)oxy]-4-chlorophenyl]-3,5-dichloro-2,3′-bipyridine-6′-carboxylate in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653276B2
Source datasetuspto-grants-2014_02
ORD IDord-15aa13f6476e404f8ea33bd321b89329
Source noteuspto-grants-2014_02