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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432109Generated: October 25, 2026

Oxygen → Tert-butyl 2-(but-3-enylamino)-6-methylisonicotinate

https://huagongshe.com/reaction/1432109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
Reactant3-Buten-1-amineHCID 443732—
Reactant2-Chloro-6-methyl-isonicotinic acid tert-butyl esterHCID 86040366—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 2-(but-3-enylamino)-6-methylisonicotinateHCID 68545468—

Reaction Conditions

Temperature60 °C

Reaction Steps

Under rigorous exclusion of oxygen a mixture of 200 mg (0.88 mmol) 2-chloro-6-methyl-isonicotinic acid tert-butyl ester, 10 mg palladium(II)acetate (0.044 mmol), 27 mg (0.44 mol) BINAP (R(+)-2,2-bis(diphenylphosphino)-1,1-binaphtalene) and 62 mg (0.88 mmol) but-3-enylamine in 10 ml toluene is heated at 60° C. for 4 h. The mixture is diluted with EtOAc, washed with 10% aqueous NaHCO3 and water, dried with sodium sulfate and evaporated. Chromatography of the product on silica gel (hexane/EtOAc 9:1) yields the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612055B2
Source datasetuspto-grants-2009_11
ORD IDord-d15b92506bb348ecaa7e92541511aab2
Source noteuspto-grants-2009_11