Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982878Generated: October 25, 2026

Sodium Carbonate → 1H-Indole-6-carboxamide

https://huagongshe.com/reaction/1982878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantLithium ChlorideHCID 433294—
Reactant2-Formyl-4-methoxybenzeneboronic acidHCID 2734365—
Reactant2-bromo-3-cyclohexyl-N-(dimethylsulfamoyl)-1H-indole-6-carboxamideHCID 58765150—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventToluene ethanolHCID 21863594—
Product1H-Indole-6-carboxamideHCID 594837—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a slurried solution of 2-bromo-3-cyclohexyl-N-[(dimethylamino)sulfonyl]-indole-6-carboxamide (54.0 g, 126 mmol), 4-methoxy-2-formylphenylboronic acid (29.5 g, 164 mmol) and LiCl (13.3 g, 315 mmol) in EtOH/toluene (1:1, 1 L) was added a solution of Na2CO3 (40.1 g, 379 mmol) in water (380 mL). The reaction mixture was stirred 10 min. and then Pd(PPh3)4 (11.3 g, 10.0 mmol) was added. The reaction solution was flushed with nitrogen and heated at 70° C. (internal monitoring) overnight and then cooled to rt. The reaction was diluted with EtOAc (1 L) and EtOH (100 mL), washed carefully with 1N aqueous HCl (1 L) and brine (500 mL), dried (MgSO4), filtered and concentrated. The residual solids were stirred with Et2O (600 mL) for 1 h and collected by filtration to yield 1H-indole-6-carboxamide, 3-cyclohexyl-N-[(dimethylamino)sulfonyl]-2-(2-formyl-4-methoxyphenyl)- (52.8 g, 109 mmol, 87%) as a yellow powder which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541352B2
Source datasetuspto-grants-2009_06
ORD IDord-de88557b73624a1d9da186e37bacab03
Source noteuspto-grants-2009_06