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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219263Generated: October 30, 2026

1-Naphthalenesulfonyl chloride → HCID 11560264, compound

https://huagongshe.com/reaction/2219263

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Naphthalenesulfonyl chlorideHCID 66560—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 57438420HCID 57438420—
SolventDimethylformamideHCID 6228—
ProductHCID 11560264HCID 1156026451%

Reaction Steps

149.5 mg (0.66 mMol) of naphtalene-1-sulfonyl chloride were added to a solution of 122 mg (0.6 mMol) of 7-amino-3-(2-dimethylaminoethyl)-1H-indole in 2 ml of dimethylformamide and 116 mg of N-ethyldiisopropylamine. The reaction mixture was stirred at the room temperature for 20 hours. Then it was evaporated to dryness, slightly alkalinized with sodium bicarbonate solution and extracted with chloroform. The organic phase was repeatedly washed with water and saturated solution of sodium bicarbonate, it was separated and dried with anhydrous sodium sulfate. The organic solution was evaporated to dryness and the resulting solid was purified by chromatography, obtaining 120 mg (51%) of N-[1-(2-dimethylaminoethyl)-1H-indole-7-yl]-naphtalene-1-sulfonamide as a solid cream.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07414070B2
Source datasetuspto-grants-2008_08
ORD IDord-4c649c8f27624f438883c1121abce24e
Source noteuspto-grants-2008_08