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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493490Generated: October 30, 2026

Potassium Carbonate → N-{[3'-bromo-4'-(cyanomethoxy)-1,1'-biphenyl-4-yl]methyl}-N,1-dimethyl-1H-indole-3-carboxamide

https://huagongshe.com/reaction/493490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBromoacetonitrileHCID 11534—
ReactantN-[(3'-bromo-4'-hydroxy-1,1'-biphenyl-4-yl)methyl]-N,1-dimethyl-1H-indole-3-carboxamideHCID 68860608—
SolventDimethylformamideHCID 6228—
ProductN-{[3'-bromo-4'-(cyanomethoxy)-1,1'-biphenyl-4-yl]methyl}-N,1-dimethyl-1H-indole-3-carboxamideHCID 6886263968.3%

Reaction Steps

A mixture of N-[(3′-bromo-4′-hydroxy-1,1′-biphenyl-4-yl)methyl]-N,1-dimethyl-1H-indole-3-carboxamide (4.6 g, 10.2 mmol), prepared in the previous step, bromoacetonitrile (856 μL, 12.3 mmol) and potassium carbonate (7.0 g, 50 mmol) in 75 mL of DMF was stirred under nitrogen at room temperature for 23 h (overnight). The reaction was partitioned between ethyl acetate and water. The organic layer was separated, extracted multiple times with water, dried (MgSO4) and the solvent removed under reduced pressure to give N-{[3′-bromo-4′-(cyanomethoxy)-1,1′-biphenyl-4-yl]methyl}-N,1-dimethyl-1H-indole-3-carboxamide (3.4 g, 68%) as an off-white solid, mp 202-206° C. Elemental Analysis for C26H22BrN3O2. Calc'd: C, 63.94; H, 4.54; N, 8.60. Found: C, 50.59; H, 3.30; N, 8.00

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534894B2
Source datasetuspto-grants-2009_05
ORD IDord-552abeb49c5b4b5c96fbb789b68765ca
Source noteuspto-grants-2009_05