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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355658Generated: October 31, 2026

Sodium hydride → 6-Bromo-1-(4-dimethylsulfamoyl-benzyl)-2-oxo-1,2-dihydro-indole-3,3-dicarboxylic acid di-tert-butyl ester

https://huagongshe.com/reaction/1355658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-(Bromomethyl)-N,N-dimethylbenzenesulfonamideHCID 11044082—
Reactant6-Bromo-2-oxo-1,2-dihydro-indole-3,3-dicarboxylic acid di-tert-butyl esterHCID 70034338—
SolventDimethylformamideHCID 6228—
Product6-Bromo-1-(4-dimethylsulfamoyl-benzyl)-2-oxo-1,2-dihydro-indole-3,3-dicarboxylic acid di-tert-butyl esterHCID 70032170114.2%

Reaction Steps

6-Bromo-2-oxo-1,2-dihydro-indole-3,3-dicarboxylic acid di-tert-butyl ester (5.10 g, 12.4 mmol) was dissolved in 40 ml of anhydrous N,N-dimethylformamide (DMF) under an atmosphere of dry N2. The solution was cooled to 0° C. after which time 60% sodium hydride in oil (500 mg, 12.4 mmol) was added and the solution was then stirred for 15 minutes at this temperature. The reaction mixture was the warmed to ambient temperature and stirred for 15 minutes after which time 4-bromomethyl-N,N-dimethyl-benzenesulfonamide (3.44 g, 12.4 mmol) was added. The mixture was stirred overnight after which time it was concentrated under vacuum and partitioned between DCM and water. The DCM layer was washed 3 more times with water, once with brine, dried over MgSO4, filtered and concentrated under vacuum to give 8.63 g of the titled compound as a yellow solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586447B1
Source datasetuspto-grants-2003_07
ORD IDord-1e2bd8fd3cdd4f49bff0f5aae27a6315
Source noteuspto-grants-2003_07