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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221086Generated: October 29, 2026

Methanol → tert-Butyl 5-phenylpyridin-2-ylcarbamate

https://huagongshe.com/reaction/2221086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
Reactant2-(Boc-amino)-5-bromopyridineHCID 16217843—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 5-phenylpyridin-2-ylcarbamateHCID 5867153872%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 1B (7.65 g, 28 mmol) in THF (50 mL)-MeOH (50 mL) at RT was added phenylboronic acid (6.83 g, 56 mmol), PXPd (500 mg, 0.93 mmol), followed by K2CO3 (15.5 g, 112 mmol). The reaction mixture was stirred at 70° C. in a preheated oil bath for 1 h. After this time, the reaction mixture was cooled to RT. The reaction mixture was poured into water (100 mL), and the resultant mixture was extracted with EtOAc (3×100 mL). The combined organic layers were washed with saturated NaCl. The organic layer was dried (Na2SO4), filtered and concentrated. The resulting residue was purified by silica gel (120 g) column chromatography eluting with a gradient of EtOAc (0-60%) in hexane to give the title compound as an off-white solid (5.4 g, 72%). LC/MS (method A): retention time=3.07 min, (M+H)+=271.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368458B2
Source datasetuspto-grants-2008_05
ORD IDord-89b5d69a5aa34010b45e5ccad462765b
Source noteuspto-grants-2008_05