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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367938Generated: October 25, 2026

(Pyridin-4-yl)boronic acid → 2-Amino-3-nitro-5-pyridin-4-yl-benzoic acid methyl ester

https://huagongshe.com/reaction/1367938

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Pyridin-4-yl)boronic acidHCID 2734379—
ReactantMethyl 2-amino-5-bromo-3-nitrobenzoateHCID 17984898—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSodium CarbonateHCID 10340—
Product2-Amino-3-nitro-5-pyridin-4-yl-benzoic acid methyl esterHCID 6694053350.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 1.0 g (3.6 mmol) of 2-amino-5-bromo-3-nitro-benzoic acid methyl ester, 0.9 g (7.2 mmol) of pyridine-4-boronic acid, 0.42 g (0.36 mmol) of (tetrakistriphenyl phosphine) palladium (0) in 50 mL of DME and 8.4 mL of 2 N Na2CO3 was degassed with nitrogen for 20 min and then heated at 90° C. for 12 h. The reaction mixture was cooled to r.t., extracted with ethyl acetate (100 mL), washed with water, brine, dried over magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure. The residue was purified by column chromatography using 8:2 hexane and ethyl acetate to afford 0.5 g (50%) of the 2-Amino-3-nitro-5-pyridin-4-yl-benzoic acid methyl ester as a solid. LCMS: 273 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893267B2
Source datasetuspto-grants-2011_02
ORD IDord-1d118ea74f7c481fab8fc23f8ce4d942
Source noteuspto-grants-2011_02