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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982794Generated: November 3, 2026

Benzenesulfonyl chloride → 4-(2-Chloroethoxy)-1-(phenylsulfonyl)-1H-indazole

https://huagongshe.com/reaction/1982794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium hydrideHCID 24758—
ReactantHCID 22326703HCID 22326703—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Chloroethoxy)-1-(phenylsulfonyl)-1H-indazoleHCID 12018439—

Reaction Steps

A stirred solution of 4-(2-chloroethoxy)-1H-indazole (1.1 g, 5.59 mmol) in tetrahydrofuran is treated with NaH (0.335 g, 60% in mineral oil, 8.39 mmol) under nitrogen at room temperature, stirred for 30 minutes, treated with benzenesulfonyl chloride (0.86 ml, 6.71 mmol), stirred at room temperature for 18 hr, quenched with water and diluted with ethyl acetate. The phases are separated and the organic phase is washed with water and brine, dried over MgSO4 and concentrated in vacuo. The resultant residue is purified by flash chromatography (silica gel, EtOAc/hexane: 3/7) to give the desired product as a white solid, 1.75 g (93%), mp 102-104° C., identified by NMR and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541358B2
Source datasetuspto-grants-2009_06
ORD IDord-ded6b563ca714189becc6875d3d8a529
Source noteuspto-grants-2009_06