HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1425672Erstellt: 26. Oktober 2026
Diisopropylcarbodiimide → 3-(4,5-Dimethoxy-2-nitro benzyloxycarbonyl-amino)-butyric acid 4-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-phenyl ester
https://huagongshe.com/reaction/1425672
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diisopropylcarbodiimide | HCID 12734 | — |
| Edukt | 1-(4-hydroxyphenyl)-1H-pyrrole-2,5-dione | HCID 81734 | — |
| Edukt | 3-(4,5-Dimethoxy-2-nitro-benzyloxycarbonylamino)-butyric acid | HCID 59336635 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-(4,5-Dimethoxy-2-nitro benzyloxycarbonyl-amino)-butyric acid 4-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-phenyl ester | HCID 59336582 | — |
Reaktionsschritte
1-(4-Hydroxy-phenyl)-pyrrole-2,5-dione (1 mmol), NHS (1.0 mmol) and 3-(4,5-dimethoxy-2-nitro-benzyloxycarbonylamino)-butyric acid (1 mmol) is dissolved in THF (3 mL). The solution is cooled to 0° C. and treated dropwise with DIC (1.2 mmol). The cooling bath is removed after 1 hour and the reaction mixture is left at room temperature o/n. The solvent is evaporated in vacuo and the pure product (3-(4,5-dimethoxy-2-nitro benzyloxycarbonyl-amino)-butyric acid 4-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-phenyl ester) is isolated by silica column purification using EtOAc-heptane (1:4 then 1:2 then 1:1) as eluent.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08932992B2 |
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| Quelldatensatz | uspto-grants-2015_01 |
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| ORD ID | ord-ccf20c989e3f40848e3ce597701791db |
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| Quellennotiz | uspto-grants-2015_01 |
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