HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2389859Erstellt: 26. Oktober 2026
Hydrochloric Acid → 2-[2-(11H-Indolo[3,2-c]quinolin-6-ylamino)ethylamino]ethanol hydrochloride
https://huagongshe.com/reaction/2389859
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Isatin | HCID 7054 | — |
| Edukt | N-(2-Hydroxyethyl)ethylenediamine | HCID 8112 | — |
| Edukt | 6-Chloro-11H-indolo[3,2-c]quinoline | HCID 5410307 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Glycol monoethyl ether | HCID 8076 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-[2-(11H-Indolo[3,2-c]quinolin-6-ylamino)ethylamino]ethanol hydrochloride | HCID 68670524 | 70% |
Reaktionsschritte
A mixture of compound 4a as obtained from the above Synthesis Ex. 1 (0.50 g, 2 mmol) and N-(2-hydroxyethyl)ethylenediamine (0.63 g, 6 mmol) in 2-ethoxyethanol (5 mL) was heated at 140-150° C. for 24 hrs (by TLC monitoring). After cooling, the reaction mixture was evaporated in vacuo to give a residue, which was dissolved in EA (50 mL). The EA layer was washed with H2O and brine and then dried (MgSO4). Concentration of the EA layer gave a residue, which was dissolved in MeOH (10 mL) and then added with a solution of 6N HCl at 0° C., followed by stirring at room temperature for 8 hrs. The resultant precipitate was filtered off, washed with MeOH, and dried at 90° C. under reduced pressure for 24 hrs to give the title compound 9 (0.50 g, 70% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08273760B2 |
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| Quelldatensatz | uspto-grants-2012_09 |
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| ORD ID | ord-4f8e9553cc7d47a1a546fd042eb9d488 |
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| Quellennotiz | uspto-grants-2012_09 |
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