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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233611Generated: November 1, 2026

Sodium Chloride → 2-Amino-3-cyano-4-methyl-5-phenylcarbonylpyridine

https://huagongshe.com/reaction/233611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantTriethylamineHCID 8471—
Reactant1,4-DioxaneHCID 31275—
ReactantPhenylboronic AcidHCID 66827—
Reactant2-Amino-5-iodo-4-methylnicotinonitrileHCID 11391265—
ReactantHCID 178418416HCID 178418416—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Product2-Amino-3-cyano-4-methyl-5-phenylcarbonylpyridineHCID 19707207—

Reaction Conditions

Temperature65 °C

Reaction Steps

A solution of 4.9 grams (0.019 mole) of 2-amino-3-cyano-5-iodo-4-methylpyridine (prepared as in Step E of Example 9) in 75 mL of dioxane is stirred, and gaseous carbon monoxide is bubbled in during a 15 minute period. While maintaining a carbon monoxide atmosphere, 4.7 grams (0.039 mole) of phenylboronic acid (commercially available), 6.8 mL (0.048 mole) of triethylamine, and 0.5 gram (catalyst) of palladium(II) acetate are in turn added. To maintain the carbon monoxide atmosphere, a balloon filled with carbon monoxide gas is then attached to the reaction vessel. The reaction mixture is then warmed to 65° C. where it is stirred for about 20 hours. The reaction mixture is then poured into a mixture of 300 mL of water and 100 mL of aqueous saturated sodium chloride solution. This mixture is extracted with two 150 mL portions of ethyl acetate. The combined extracts are dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure to a residue. The residue is purified using column chromatography, yielding 2-amino-3-cyano-4-methyl-5-phenylcarbonylpyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05593998
Source datasetuspto-grants-1997_01
ORD IDord-e7c523036a4c4054b75c258d00618734
Source noteuspto-grants-1997_01