HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1664081Erstellt: 25. Oktober 2026
N-methyl-2-pyrrolidone → 2,2'-(Disulphanediyldiethane-2,1-diyl)bis(6-chloro-1H-benzo[de]-isoquinoline-1,3(2H)-dione)
https://huagongshe.com/reaction/1664081
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Edukt | 1H,3H-Naphtho[1,8-cd]pyran-1,3-dione, 6-chloro- | HCID 77672 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 2-[(2-Aminoethyl)disulfanyl]ethan-1-amine hydrochloride | HCID 167628 | — |
| Produkt | 2,2'-(Disulphanediyldiethane-2,1-diyl)bis(6-chloro-1H-benzo[de]-isoquinoline-1,3(2H)-dione) | HCID 59428884 | — |
Reaktionsschritte
9.30 g of 6-chloro-1H,3H-benzo[de]isochromene-1 ,3-dione and 4.46 g of hydrochlorided cystamine hydrochloride are suspended in 50 ml of N-methylpyrrolidone (NMP). 5.5 g of diisopropylethylamine are added and the mixture is heated with stirring at 120° C. After two hours, 50 ml of NMP are added and the mixture is kept with stirring at 120° C. for 3 hours. After cooling, the precipitated product is recovered and the filtered solution is extended by addition of 200 ml of water, and a second precipitate is recovered. The precipitates are washed with water and dried. 11.46 g of white powder are recovered. The analyses show that the product is in accordance with the expected product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08038731B2 |
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| Quelldatensatz | uspto-grants-2011_10 |
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| ORD ID | ord-ee6a623d63a74f3484eefa9efffc054f |
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| Quellennotiz | uspto-grants-2011_10 |
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