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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389307Generated: October 30, 2026

Sodium hydride → HCID 25128162, compound

https://huagongshe.com/reaction/389307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Propanesulfonyl chlorideHCID 82408—
ReactantHCID 66812534HCID 66812534—
SolventTetrahydrofuranHCID 8028—
ProductHCID 25128162HCID 2512816212.2%

Reaction Steps

To the suspension of 60% Sodium hydride (76 mg, 0.0019 mole) in Tetrahydrofuran (2 ml), the solution of 3-[4-(7-Methoxy-6-methyl-indan-4-ylmethyl)-3,5-dimethyl-pyrazol-1-yl]-propionamide (500 mg, 0.00146 mole) in Tetrahydrofuran (5 ml) was added at room temperature and stirred for 20 minutes. A solution of Isopropyl sulfonyl chloride (0.18 ml, 0.0016 moles) in Tetrahydrofuran (3 ml) was added at 0-5° C. and stirred at 15-25° C. for 3 hours. Tetrahydrofuran was distilled under vacuum, dilute hydrochloric acid (20 ml) was added to the reaction mixture and extracted with Ethyl Acetate (50 ml). The Ethyl acetate layer was dried over Sodium sulphate and distilled under vacuum to give a crude product which was purified by column chromatography using Ethylacetate as a mobile phase. The fractions were distilled to give 80 mg of desired compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378118B2
Source datasetuspto-grants-2013_02
ORD IDord-618c7d5c975f46ba96970b6ab1316eda
Source noteuspto-grants-2013_02