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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754504Generated: October 29, 2026

Sodium hydride → HCID 45273621, compound

https://huagongshe.com/reaction/1754504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-Chloro-3-cyanobenzenesulfonyl chlorideHCID 18072853—
Reactantmethyl 2-(2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)acetateHCID 67218699—
SolventTetrahydrofuranHCID 8028—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
ProductHCID 45273621HCID 45273621—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred, ice-cooled (0° C.) suspension of sodium hydride (15.8 mg of a 60% dispersion in mineral oil, 0.411 mmol) in dry THF (2 ml) under an inert atmosphere of Argon is added dropwise (2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-acetic acid methyl ester ((0.06 g, 0.294 mmol) in THF/DMF (4 ml of a 3:1 mixture). The reaction mixture is stirred at 0° C. for 45 minutes and then treated with 4-chloro-3-cyano-benzenesulfonyl chloride (97.1 mg, 0.411 mmol) in dry THF (3 ml). Stirring continued at 0° C. for 15 minutes and then the reaction mixture is poured onto water (30 ml) and extracted with ethyl acetate (100 ml). The organic portion is separated and washed brine (50 ml), dried (MgS04) and concentrated in vacuo. The resulting crude is purified by chromatography on silica eluting with iso-hexane/ethyl acetate (0%-20% ethyl acetate) to yield the titled product. (MH+404)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169251B2
Source datasetuspto-grants-2015_10
ORD IDord-82255923d8fa4442abc1c472936ff5a7
Source noteuspto-grants-2015_10