HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 613354Erstellt: 25. Oktober 2026
1,2-Dichloroethane → Methyl (+/-)-7-[[bis[2-(4-pyridinyl)ethyl]amino]carbonyl]-4-methyl-3-oxo-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine-2-acetate
https://huagongshe.com/reaction/613354
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,2-Dichloroethane | HCID 11 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Bis[2-(4-pyridyl)ethyl]amine | HCID 416637 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | HCID 23505570 | HCID 23505570 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Methyl (+/-)-7-[[bis[2-(4-pyridinyl)ethyl]amino]carbonyl]-4-methyl-3-oxo-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine-2-acetate | HCID 53801004 | 93% |
Reaktionsschritte
Diisopropylethylamine (0.35 g, 2.7 mmole) was added in one portion to a stirred mixture of bis [2-(4-pyridyl)ethyl]amine (0.37 g, 1.65 mmole), methyl (±)-7-carboxy-4-methyl-3-oxo-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine-2-acetate (0.44 g, 1.50 mmole), EDC (0.34 g, 1.8 mmole), and HOBT . H2O (0.24 g, 1.8 mmole) in DMF (8 mL) at 0° C. under argon, and the reaction was allowed to warm to RT. After 19.5 h, the reaction was poured into a mixture of ice water (100 g) and 5% NaHCO3 (10 mL) and extracted with CH2Cl2 (2×100 mL). The combined organic layers were washed with 5% NaHCO3 (50 mL), dried (MgSO4), and concentrated. Chromatography on silica gel (7% MeOH/CH2Cl2) gave the title compound (0.7 g, 88%). MS (ES) m/e 502.4 (M+H)+. c) (±)-7-[[Bis[2-(4-pyridinyl)ethyl]amino]carbonyl]-4-methyl-3-oxo-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine-2-acetic acid
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06008214 |
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| Quelldatensatz | uspto-grants-1999_12 |
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| ORD ID | ord-92fd1c0b6d984f06bc03d6daca9b551b |
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| Quellennotiz | uspto-grants-1999_12 |
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