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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8338Generated: October 25, 2026

Benzenesulfonyl chloride → N-Benzenesulfonyl-5-(4-methylpiperazin-1-yl)-indole

https://huagongshe.com/reaction/8338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium HydroxideHCID 14798—
Reactant5-(4-Methylpiperazin-1-yl)-1H-indoleHCID 22015405—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventDichloromethaneHCID 6344—
ProductN-Benzenesulfonyl-5-(4-methylpiperazin-1-yl)-indoleHCID 2201541266%

Reaction Steps

5-(4-Methylpiperazin-1-yl)-indole (215 mg, 1 mmol), benzenesulfonylchloride (265 mg, 1.5 mmol) and Aliquat 336 (10 mg) were dissolved in DCM (10 mL). Aqueous NaOH (20%, 2 mL) was added and the mixture was stirred vigorously for 6 h. The organic layer was separated, dried and concentrated to give the crude as an oil that was purified on a silica column using DCM and MeOH as eluent. The pure fractions were concentrated to give an oil (260 mg, 0.66 mmol) 1H NMR (CDCl3) δ 2.35 (3 H, s), 2.59 (4 H, t, J=5), 3.18 (4 H, t, J=5), 6.57 (1 H, d, J=4), 6.98–7.03 (2 H, m), 7.38–7.54 (4 H, m), 7.82–7.90 (3 H, m); MS (posES-FIA) 355.1345 M+; Purity (HPLC chromsil C18) >98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087750B2
Source datasetuspto-grants-2006_08
ORD IDord-ed49fbd1fa8449b196577007bf5b1c3e
Source noteuspto-grants-2006_08