HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18432Erstellt: 23. Oktober 2026
3-Chloropropanesulphonyl chloride → N-{5-[3-(1,1-dioxido-2-isothiazolidinyl)phenyl]-2,3-dihydro-1H-inden-2-yl}-2-propanesulfonamide
https://huagongshe.com/de/reaction/18432
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 3-Chloropropanesulphonyl chloride | HCID 15410 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | N-[5-(3-aminophenyl)-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamide | HCID 46899970 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-{5-[3-(1,1-dioxido-2-isothiazolidinyl)phenyl]-2,3-dihydro-1H-inden-2-yl}-2-propanesulfonamide | HCID 11575686 | 9,2% |
Reaktionsschritte
A mixture of N-[5-(3-aminophenyl)-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamide (100 mg, 0.30 mmol), and diisopropylethylamine (79 mg, 0.61 mmol), in dry dimethylformamide (2 ml) was treated with 3-chloropropanesulfonyl chloride (54 mg, 0.30 mmol) and stirred at room temperature for 1 h. Sodium hydride (60% dispersion in oil, 15 mg, 0.38 mmol) was added and the mixture stirred at 60° C. for 0.5 h. The reaction mix was cooled then partitioned between dichloromethane and 0.5M hydrochloric acid, and the organic layer was evaporated under reduced pressure to give a brown oil which was purified by column chromatography on a 5 g isolute silica sep-pak column eluting from 0-50% ethyl acetate in 40-60° C. petroleum ether to give the title compound as a yellow oil (12 mg, 9%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07741351B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-cf415d9399974ffea9b7863d9a6fca64 |
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| Quellennotiz | uspto-grants-2010_06 |
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