HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 45709Erstellt: 25. Oktober 2026
Ethylenediamine → N-(2-aminoethyl)-3-(6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)benzenesulfonamide
https://huagongshe.com/reaction/45709
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethylenediamine | HCID 3301 | — |
| Edukt | 3-(6,8-Dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)benzene-1-sulfonyl chloride | HCID 86672330 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | dichloromethane N,N-dimethylformamide | HCID 22350042 | — |
| Produkt | N-(2-aminoethyl)-3-(6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)benzenesulfonamide | HCID 67457253 | 83,5% |
Reaktionsschritte
Into a 50-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 3-(6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)benzene-1-sulfonyl chloride (intermediate 1.6) (100 mg, 0.26 mmol, 1.00 equiv) in DCM (5 mL). This was followed by the addition of a solution of ethane-1,2-diamine (307 mg, 5.11 mmol, 19.96 equiv) in DCM/DMF (10/1 mL). The resulting solution was stirred for 5 h at room temperature. The mixture was concentrated under vacuum. The resulting solution was diluted with 50 mL of ethyl acetate and washed with 2×10 mL of water and then 1×10 mL of Brine. The organic layer was dried over anhydrous sodium sulfate and concentrated under vacuum to afford 90 mg (76%) of N-(2-aminoethyl)-3-(6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)benzenesulfonamide as yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08541448B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-ea30e5dadb2045db8e37a5e6578430cd |
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| Quellennotiz | uspto-grants-2013_09 |
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