HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1512702Erstellt: 25. Oktober 2026
Ammonia → Benzyl 2-{[2-amino-3-(aminocarbonyl)phenyl]amino}-1,1-dimethyl-2-oxoethylcarbamate
https://huagongshe.com/reaction/1512702
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonia | HCID 222 | — |
| Edukt | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Edukt | N-((Benzyloxy)carbonyl)-2-methylalanine | HCID 294936 | — |
| Edukt | 2,3-Diaminobenzamide dihydrochloride | HCID 53422807 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Benzyl 2-{[2-amino-3-(aminocarbonyl)phenyl]amino}-1,1-dimethyl-2-oxoethylcarbamate | HCID 68512848 | — |
Reaktionsschritte
2-{[(Benzyloxy)carbonyl]amino}-2-methylpropanoic acid (5.18 g, 21.83 mmol) in a mixture of pyridine (25 mL) and DMF (25 mL) was treated with 1,1′-carbonyldiimidazole (3.72 g, 22.92 mmol) and heated at 40° C. for 2 hours. 2,3-Diaminobenzamide dihydrochloride (4.89 g, 21.83 mmol), prepared as described in WO0026192, was added and the mixture was stirred at room temperature overnight. The solvents were removed under vacuum and the residue was partitioned between ethyl acetate and diluted sodium bicarbonate aqueous solution. The formed slightly yellow solid material was collected by filtration, washed with water and ethyl acetate, and dried to give Example 1A. MS (DCI/NH3) m/z 371 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08217070B2 |
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| Quelldatensatz | uspto-grants-2012_07 |
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| ORD ID | ord-f3f3a3a79c3241adb0da397c6bef082a |
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| Quellennotiz | uspto-grants-2012_07 |
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