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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600316Generated: October 25, 2026

Potassium Carbonate → (S)-tert-Butyl 2-((S)-1-amino-3-(4-(6-cyanopyridin-3-yl)phenyl)-1-oxopropan-2-ylcarbamoyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/600316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromopyridine-2-carbonitrileHCID 817154—
Reactant(S)-tert-Butyl 2-((S)-1-amino-1-oxo-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-2-ylcarbamoyl)piperidine-1-carboxylateHCID 57999680—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product(S)-tert-Butyl 2-((S)-1-amino-3-(4-(6-cyanopyridin-3-yl)phenyl)-1-oxopropan-2-ylcarbamoyl)piperidine-1-carboxylateHCID 5799964879.1%

Reaction Steps

A solution of (S)-tert-butyl 2-((S)-1-amino-1-oxo-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-2-ylcarbamoyl)piperidine-1-carboxylate (0.150 g) in dioxane (1 mL) was added to a stirred solution of 5-bromopicolinonitrile (0.055 g) and bis[bis(1,2-diphenylphosphino)ethane]palladium (0) (0.003 g) in dioxane (1 mL) under nitrogen. The resulting mixture was stirred for 10 min. A solution of potassium carbonate (0.124 g) in water (0.75 mL) was added and the resulting solution was stirred at 75° C. for 16 h. The cooled mixture was evaporated to dryness. The residue was taken up in ethyl acetate and washed with saturated brine, dried over sodium sulfate and adsorbed onto silica. The crude product was purified by flash silica chromatography, eluting with 3:1 ethyl acetate/isohexane). Pure fractions were evaporated to dryness to afford the subtitle compound (0.113 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902181B2
Source datasetuspto-grants-2011_03
ORD IDord-a5b49953c7bf43ff903db367a6fe3e9b
Source noteuspto-grants-2011_03