HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 12630Erstellt: 25. Oktober 2026
Ammonia → Benzyl 2-{[2-amino-3-(aminocarbonyl)phenyl]amino}-1,1-dimethyl-2-oxoethylcarbamate
https://huagongshe.com/reaction/12630
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 | HCID 10487029 | — |
| 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 dihydrochlolide (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 | US07728026B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-9c25fc59113f4ee5ad6fdc1b8bb23676 |
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| Quellennotiz | uspto-grants-2010_06 |
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