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HRID 1617Erstellt: 23. Oktober 2026
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → N-Carboxy-[1-butyl-4-piperidinylmethyl]-carbazole
https://huagongshe.com/de/reaction/1617
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Edukt | N-Carboxy-[1-butyl-4-piperidinylmethyl]-1,2,3,4,4a,9a-hexahydrocarbazole | HCID 67817506 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | N-Carboxy-[1-butyl-4-piperidinylmethyl]-carbazole | HCID 19691861 | — |
Reaktionsschritte
N-Carboxy-[1-butylpiperidin-4-ylmethyl]-1,2,3,4,4a,9a-hexahydrocarbazole (0.530 g, 1.32 mmol) was dissolved in chloroform (25 ml) and treated with 2,3-dichloro-5,6-dicyano-1, 4-benzoquinone (0.329 g, 1.58 mmol) with stirring. The mixture was heated to reflux for 12 hours, cooled, and more 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (0.329 g 1.58 mmol) added with stirring. The mixture was heated to reflux for 12 hours, cooled and evaporated under reduced pressure. The residue was purified by Silica-gel chromatography, eluting with 2%MeOH/CHCl3 to give the title compounds as 3:1 mixture. The mixture was separated by preparative HPLC using a Waters Micro Bondapak C18 (300 mm×7.8 mm) column and eluting with 75:25 MeCN: 0.1M Ammonium Acetate (pH 5.0).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05726187 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-4f6016db03934931aac4c3c4d6a66417 |
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| Quellennotiz | uspto-grants-1998_03 |
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