Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570589Generated: November 1, 2026

Sodium hydride → HCID 67087949, compound

https://huagongshe.com/reaction/570589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2,4-Dimethoxybenzenesulfonyl chlorideHCID 2734626—
ReactantHCID 67087991HCID 67087991—
SolventDimethylformamideHCID 6228—
ProductHCID 67087949HCID 67087949102.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

3.2 g (79 mmol) of sodium hydride (60% dispersion in mineral oil) were added in portions to a solution of 20 g (66 mmol) of 3-amino-5-chloro-3-(2-ethoxypyridin-3-yl)-1,3-dihydroindol-2-one in 50 ml of anhydrous dimethylformamide under a nitrogen atmosphere and while cooling in an ice bath. The mixture was stirred at 0° C. for 10 min and then 18.7 g (79 mmol) of 2,4-dimethoxybenzenesulfonyl chloride were added, and the mixture was stirred at room temperature for 30 min. The reaction mixture was poured into ice-water and then extracted with ethyl acetate. The organic phase was washed with saturated sodium chloride solution and dried over magnesium sulfate, and the solvent was evaporated. The residue was purified by chromatography on silica gel (120 g Redisep cartridge, mobile phase gradient from 2 to 25% dichloromethane in ethyl acetate). 34 g of the title compound were obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023854B2
Source datasetuspto-grants-2015_05
ORD IDord-cfbf35fcd0164b2daa14763f8ce1abc1
Source noteuspto-grants-2015_05