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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748586Generated: October 30, 2026

Benzophenone imine → HCID 86692536, compound

https://huagongshe.com/reaction/1748586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenone imineHCID 136809—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
Reactant(1,1'-Binaphthalen)-2-yldi-tert-butylphosphineHCID 2734941—
ReactantHydroxylamine monohydrateHCID 22235265—
ReactantHCID 86692537HCID 86692537—
Reactantsodium 2-methylpropan-2-olateHCID 178418730—
Catalystpalladium(II) acetateHCID 167845—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 86692536HCID 86692536—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a suspension of 4-(5-bromo-3-methylpyridin-2-yl)-1,2,3,6-tetrahydropyridine-1-carboxylic acid tert-butyl ester (4.83 g), palladium(II) acetate (384 mg), (±)-2-(di-tert-butylphosphino)-1,1′-binaphthyl (1.06 g), and tert-butoxysodium (1.97 g) in toluene (34 ml) was added benzophenone imine (2.29 ml), stirred at 120° C. for 3.5 hours, then ethanol (34 ml), water (34 ml), hydroxylamine monohydrate (4.0 g), and sodium acetate (6.73 g) were added thereto at room temperature, and stirred at room temperature for 4 hours. To the reaction solution was added a saturated aqueous solution of sodium hydrogen carbonate, extracted with ethyl acetate, washed with saturated brine, dried over anhydrous sodium sulfate, and then the solvent was evaporated in vacuo. The obtained residue was purified with basic silica gel chromatography (n-hexane/ethyl acetate) to give 4-(5-amino-3-methylpyridin-2-yl)-1,2,3,6-tetrahydropyridine-1-carboxylic acid tert-butyl ester (2.4 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150555B2
Source datasetuspto-grants-2015_10
ORD IDord-d077b449293147c3ab3a8dd2f9307842
Source noteuspto-grants-2015_10