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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49996Generated: October 29, 2026

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

https://huagongshe.com/reaction/49996

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 numberUS06710069B2
Source datasetuspto-grants-2004_03
ORD IDord-b9ac61d885c64c10858c84ef7b91e637
Source noteuspto-grants-2004_03