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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888998Generated: October 31, 2026

2-Methyl-2-butanol → 2-[(5-tert-butyl-2-methylphenyl)amino]-6-[4-(1H-imidazol-1-yl)piperidin-1-yl]-N,N-dimethylisonicotinamide

https://huagongshe.com/reaction/888998

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-butanolHCID 6405—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant5-tert-Butyl-2-methylanilineHCID 13089979—
Reactant2-chloro-6-[4-(1H-imidazol-1-yl)piperidin-1-yl]-N,N-dimethylisonicotinamideHCID 86639110—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product2-[(5-tert-butyl-2-methylphenyl)amino]-6-[4-(1H-imidazol-1-yl)piperidin-1-yl]-N,N-dimethylisonicotinamideHCID 59191959—

Reaction Conditions

Temperature100 °C

Reaction Steps

2-chloro-6-[4-(1H-imidazol-1-yl)piperidin-1-yl]-N,N-dimethylisonicotinamide (250 mg, 0.749 mmol), 5-tert-butyl-2-methylaniline (132 mg, 0.809 mmol), 2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl (187 mg, 0.392 mmol), Pd2(dba)3 (70 mg, 0.076 mmol) and potassium carbonate (119 mg, 0.861 mmol) were combined in a vial, sealed, and put under an atmosphere of N2. Degassed t-amyl alcohol (3 ml) was added. The mixture was stirred at 100° C. overnight.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252803B2
Source datasetuspto-grants-2012_08
ORD IDord-e8625ad4e2194824b8f0841ee706d526
Source noteuspto-grants-2012_08