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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260627Generated: November 2, 2026

Sodium hydride → HCID 67219495, compound

https://huagongshe.com/reaction/1260627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-(Methylsulfonyl)benzyl BromideHCID 2733581—
ReactantHCID 67219047HCID 67219047—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67219495HCID 67219495—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) stirred solution of (4-chloro-2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-acetic acid methyl ester (0.1 g, 0.42 mmol) in dry DMF (2.5 ml) is added sodium hydride (0.019 g of a 60% dispersion in mineral oil, 0.47 mmol). After stirring at room temperature for 5 hours, the reaction mixture is re-cooled to 0° C. and treated with 4-methylsulfonylbenzyl bromide (0.105 g, 0.42 mmol). The resulting mixture is stirred and allowed to warm to room temperature overnight. The reaction mixture is diluted with water (3 ml) and extracted with ether (3×15 ml). The organic portions are combined, washed with water, dried (Na2SO4) and concentrated in vacuo. The resulting crude residue is loaded on a pre-packed packed Isolute™ silica column and eluted with iso-hexane:ethyl acetate (1:8) to yield the titled compound as a white powder. (MH+ 407).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470848B2
Source datasetuspto-grants-2013_06
ORD IDord-6f4335c9b4cd4b9b98129a00c9a60c24
Source noteuspto-grants-2013_06