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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868121Generated: October 31, 2026

Binap, (A+-)- → 5-[(3R)-3-methylpiperazin-1-yl]pyridine-2-carbonitrile

https://huagongshe.com/reaction/1868121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBinap, (A+-)-HCID 634876—
Reactant5-Bromopyridine-2-carbonitrileHCID 817154—
Reactant2-Methylpiperazine, (R)-HCID 7330434—
ReactantSodium t-butoxideHCID 23676156—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product5-[(3R)-3-methylpiperazin-1-yl]pyridine-2-carbonitrileHCID 44249586—

Reaction Steps

A mixture of (R)-2-methyl-piperazine (1.0 g, 9.98 mmol), 5-bromo 2-cyanopyridine (1.66 g, 9.08 mmol), tris(dibenzylidineacetone)dipalladium (0) (83.15 mg, 0.0908 mmol), rac-2,2′-bis(diphenylphosphino)-1,1′-binaphtyl (169.37 mg, 0.272 mmol) and sodium tert-butoxide (1.09 g, 11.35 mmol) were charged to a microwave vial. Toluene (10.0 mL) was introduced under nitrogen atmosphere and the reaction mixture was irradiated at 110° C. for 35 minutes. Reaction was complete as determined by TLC. Reaction mixtures was diluted with dichloromethane, washed with water, saturated brine then dried over Na2SO4 and concentrated. The crude product was purified via flash column chromatography to yield 5-[(3R)-3-methylpiperazin-1-yl]pyridine-2-carbonitrile as brown color oil (1.15 g, 39.1% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632838B2
Source datasetuspto-grants-2009_12
ORD IDord-e0f89058f3204bf586a657ab74b39a6f
Source noteuspto-grants-2009_12