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HRID 12630Erstellt: 25. Oktober 2026

Ammonia → Benzyl 2-{[2-amino-3-(aminocarbonyl)phenyl]amino}-1,1-dimethyl-2-oxoethylcarbamate

https://huagongshe.com/reaction/12630

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktN-((Benzyloxy)carbonyl)-2-methylalanineHCID 294936—
Edukt2,3-DiaminobenzamideHCID 10487029—
LösungsmittelPyridineHCID 1049—
LösungsmittelDimethylformamideHCID 6228—
ProduktBenzyl 2-{[2-amino-3-(aminocarbonyl)phenyl]amino}-1,1-dimethyl-2-oxoethylcarbamateHCID 68512848—

Reaktionsbedingungen

Temperatur40 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728026B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-9c25fc59113f4ee5ad6fdc1b8bb23676
Quellennotizuspto-grants-2010_06