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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252577Generated: October 31, 2026

Potassium Carbonate → HCID 59425963, compound

https://huagongshe.com/reaction/252577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl carbamateHCID 77922—
Reactant1-N,2-N-dimethylcyclohexane-1,2-diamineHCID 551074—
Reactant6-BromoindoleHCID 676493—
ReactantHCID 59425642HCID 59425642—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTolueneHCID 1140—
ProductHCID 59425963HCID 5942596384%

Reaction Conditions

Temperature110 °C

Reaction Steps

6-Bromo-2-(4-ethoxyphenyl)-1-ethyl-1H-indole-3-carbonitrile (0.74 g, 2.0 mmol), compound 831, prepared from 6-bromoindole as described in example 1Gb, is mixed with K2CO3 (0.55 g, 4.0 mmol), CuI (0.02 g, 0.1 mmol), tert-butyl carbamate (0.35 g, 3.0 mmol), N,N′-dimethylcyclohexane-1,2-diamine ligand (0.028 g, 0.2 mmol) and anhydrous toluene (5.0 mL) in a sealed tube. The reaction system is flushed with nitrogen and then stirred at 110° C. overnight. After cooling, the solvent is replaced with dichloromethane and chromatographed (silica gel, dichloromethane) to provide [3-cyano-2-(4-ethoxy-phenyl)-1-ethyl-1H-indol-6-yl]-carbamic acid tert-butyl ester (0.68 g, 84%), compound 832.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868037B2
Source datasetuspto-grants-2011_01
ORD IDord-70cf9a0c06ab490eab7a9356ac9c2695
Source noteuspto-grants-2011_01