HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219263Generated: October 30, 2026
1-Naphthalenesulfonyl chloride → HCID 11560264, compound
https://huagongshe.com/reaction/2219263
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Naphthalenesulfonyl chloride | HCID 66560 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 57438420 | HCID 57438420 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11560264 | HCID 11560264 | 51% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07414070B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-4c649c8f27624f438883c1121abce24e |
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| Source note | uspto-grants-2008_08 |
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