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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055442Generated: November 1, 2026

Benzenesulfonyl chloride → HCID 15951554, compound

https://huagongshe.com/reaction/2055442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium hydrideHCID 24758—
ReactantHCID 15951552HCID 15951552—
SolventDimethylformamideHCID 6228—
ProductHCID 15951554HCID 1595155484.1%

Reaction Steps

To a stirred solution of 40 mg (0.11 mmol) of 1′-[(2-methyl-1H-indol-3-yl)carbonyl]-3H-spiro[2-benzofuran-1,4′-piperidine] (the preparation of which has been described in example 43) in 3 ml DMF was added 5 mg (0.11 mmol) NaH (60% in oil). The mixture was stirred at RT for 30 min. and then 24 mg (0.14 mmol) of benzenesulfonyl chloride was added. The mixture was stirred an additional hour and then poured onto water and extracted with ethyl acetate. The combined organic phases were dried over Na2SO4 and concentrated in vacuo. Re-crystallization in Et2O afforded 45 mg (80%) of 1′-{[2-methyl-1-(phenylsulfonyl)-1H-indol-3-yl]carbonyl}-3H-spiro[2-benzofuran-1,4′-piperidine] as white crystals. ES-MS m/e (%): 487.4 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332501B2
Source datasetuspto-grants-2008_02
ORD IDord-5746dc8418964db68e52c084a035e9d3
Source noteuspto-grants-2008_02