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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881123Generated: October 23, 2026

Potassium Carbonate → [6-(4-Cyano-phenyl)-pyridin-2-yl]carbamic acid tert-butyl ester

https://huagongshe.com/en/reaction/881123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Cyanophenylboronic acidHCID 2734326—
ReactantTert-butyl (6-bromopyridin-2-YL)carbamateHCID 13040380—
CatalystHCID 178418397HCID 178418397—
SolventN,N-Dimethylformamide--water (1/1)HCID 21962138—
Product[6-(4-Cyano-phenyl)-pyridin-2-yl]carbamic acid tert-butyl esterHCID 6713369160%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-cyanobenzeneboronic acid (7.35 g, 50 mmol), (6-bromo-pyridin-2-yl)carbamic acid tert-butyl ester (13.8 g, 50 mmol), Pd(Ph3P)4 (5.8 g, 0.15 mmol) and K2CO3 (10.4 g, 75 mmol) in DMF/H2O (1:1, 250 mL) was stirred under argon at 80° C. overnight. DMF was evaporated off under reduced pressure and the residue was dissolved in EtOAc (200 mL). The mixture was washed with water and brine, dried over Na2SO4, and concentrated to dryness. The residue was purified by column (Petroleum Ether/EtOAc 50:1) on silica gel to give [6-(4-cyano-phenyl)-pyridin-2-yl]carbamic acid tert-butyl ester (7.0 g, 60%). 1H NMR (300 MHz, CDCl3) δ 8.02-8.07 (m, 2 H), 7.95 (d, J=8.4 Hz, 1 H), 7.71-7.79 (m, 3 H), 7.37-7.44 (m, 2 H), 1.53 (s, 9 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993600B2
Source datasetuspto-grants-2015_03
ORD IDord-5a4402bcfdd8479494779a4346a88b75
Source noteuspto-grants-2015_03