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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 562912Generated: October 26, 2026

Methyl 2-chloropyridine-4-carboxylate → Methyl 2-(3-cyano-4-isobutoxyphenyl)isonicotinate

https://huagongshe.com/reaction/562912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-chloropyridine-4-carboxylateHCID 2736842—
Reactant(3-Cyano-4-isobutoxyphenyl)boronic acidHCID 54576546—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventSodium CarbonateHCID 10340—
ProductMethyl 2-(3-cyano-4-isobutoxyphenyl)isonicotinateHCID 6699529595.7%

Reaction Steps

In a mixed solution of 50 ml of toluene and 30 ml of a 2M aqueous sodium carbonate solution were dissolved 1.46 g of (3-cyano-4-isobutoxyphenyl)boronic acid and 1.86 g of methyl 2-chloroisonicotinate, and the resulting solution was heated at 100° C. for 1 hour in the presence of 0.49 g of tetrakis(triphenylphosphine)palladium. The reaction solution was extracted with ethyl acetate and the organic layer was washed with brine and then dried and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate:chloroform=70:15:15) to obtain 1.98 g of methyl 2-(3-cyano-4-isobutoxyphenyl)isonicotinate. (2) Then, 1.98 g of the compound was dissolved in a mixed solution of 30 ml of methanol and 70 ml of THF, and 9 ml of a 1M aqueous sodium hydroxide solution was added thereto, followed by heating at 50° C. for 1 hour.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067446B2
Source datasetuspto-grants-2011_11
ORD IDord-9d3e3f5ce118446193f19d53f19d1115
Source noteuspto-grants-2011_11