Zurück
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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktN-((Benzyloxy)carbonyl)-2-methylalanineHCID 294936—
Edukt2,3-Diaminobenzamide dihydrochlorideHCID 53422807—
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 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08217070B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-f3f3a3a79c3241adb0da397c6bef082a
Quellennotizuspto-grants-2012_07