HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 51340Erstellt: 23. Oktober 2026
Sulfuric Acid → 5-(2-Amino)ethyloxy-9-benzyl-7-methoxy-1,2,3,4-tetrahydrocarbazole-4-carboxamide
https://huagongshe.com/de/reaction/51340
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | 9-Benzyl-7-methoxy-5-cyanomethyloxy-1,2,3,4-tetrahydrocarbazole-4-carboxamide | HCID 10134925 | — |
| Edukt | lithium aluminium hydride THF | HCID 68718528 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 5-(2-Amino)ethyloxy-9-benzyl-7-methoxy-1,2,3,4-tetrahydrocarbazole-4-carboxamide | HCID 22739132 | 55,2% |
Reaktionsschritte
To 1.93 ml (1.93 mmol) 1M lithium aluminum hydride/THF in 13 ml THF at 0° C. was added H2SO4(53 μl, 0.97 mmol) dropwise over 5 min. The mixture was allowed to stir at room temperature 1 hour, then a solution of 9-benzyl-7-methoxy-5-cyanomethyloxy-1,2,3,4-tetrahydrocarbazole-4-carboxamide (0.50 g, 1.29 mmol) in 13 ml THF was added dropwise at a rate which kept the temperature below 26° C. After an additional 45 minutes, the reaction was quenched with 0.5 ml 1:1 THF/H2O, 0.75 ml 13% NaOH, and finally 80 μl H2O. The reaction was diluted with EtOAc and saturated NaHCO3, and the layers separated. The organic layer was extracted with brine, dried over sodium sulfate, and evaporated in vacuo. The residue was chromatographed on silica gel eluting with 9:1:0.1 CH2Cl2/MeOH/NH4OH to give the subtitled product (0.28 g, 55%). MS (ES+) 394
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06713645B1 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-b3c0a4b14992469eaa6f497fccc83053 |
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| Quellennotiz | uspto-grants-2004_03 |
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