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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406454Generated: October 26, 2026

Halauxifen-methyl → Methyl 4-(acetylamino)-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate

https://huagongshe.com/reaction/406454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHalauxifen-methylHCID 16656802—
Reactant4-Chloro-2-fluoro-3-methoxyphenylboronic acidHCID 44129706—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductMethyl 4-(acetylamino)-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylateHCID 67210962—

Reaction Steps

An embodiment of the present disclosure includes a method of producing methyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate. The method comprises adding methyl isobutyl ketone to an aqueous solution comprising 4-chloro-2-fluoro-3-methoxyphenylboronic acid to form an organic phase comprising the 4-chloro-2-fluoro-3-methoxyphenylboronic acid and an aqueous phase. The organic phase and the aqueous phase are separated. The 4-chloro-2-fluoro-3-methoxyphenylboronic acid is reacted with methyl 4-(acetylamino)-3,6-dichloropyridine-2-carboxylate in methyl isobutyl ketone to produce methyl 4-(acetylamino)-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate, which is deacetylated to produce methyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754110B2
Source datasetuspto-grants-2014_06
ORD IDord-faef2dc7331b4291ad9f60f89e3d5d8d
Source noteuspto-grants-2014_06