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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394892Generated: November 2, 2026

Sodium Carbonate → 11-cyclohexyl-N-[(dimethylamino)sulfonyl]-6-hydroxy-8-methoxy-6H-isoindolo[2,1-a]indole-3-carboxamide

https://huagongshe.com/reaction/1394892

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—
SolventToluene ethanolHCID 21863594—
Product11-cyclohexyl-N-[(dimethylamino)sulfonyl]-6-hydroxy-8-methoxy-6H-isoindolo[2,1-a]indole-3-carboxamideHCID 59682121—

Reaction Conditions

Temperature85 °C

Reaction Steps

To a slurried solution of 2-bromo-3-cyclohexyl-N-[(dimethylamino)sulfonyl]-indole-6-carboxamide (4.3 g, 10 mmol), 4-methoxy-2-formylphenylboronic acid (2.5 g, 14 mmol) and LiCl (11.05 g, 25 mmol) in EtOH/toluene (1:1, 80 mL) was added Pd(PPh3)4 (1.12 g, 1.0 mmol) and then 1M Na2CO3 (aq.) (30 mL, 30 mmol). The reaction solution was flushed with nitrogen and heated at 85° C. for 18 h and cooled to rt. The reaction was diluted with EtOAc (200 mL), washed with 0.5N aqueous HCl (100 mL) and brine (50 mL), dried (MgSO4), filtered and concentrated to yield 11-cyclohexyl-N-[(dimethylamino)sulfonyl]-6-hydroxy-8-methoxy-6H-isoindolo[2,1-a]indole-3-carboxamide which was used without further purification. LCMS: m/e 482 (M−H)−, ret time 1.63 min, column A, 2 minute gradient.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348425B2
Source datasetuspto-grants-2008_03
ORD IDord-20b16a45124c4b85b982bbf6f46bd65c
Source noteuspto-grants-2008_03