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HRID 12633Erstellt: 23. Oktober 2026

Isopropanol → [1-(2-Amino-3-carbamoyl-phenylcarbamoyl)-cyclohexyl]-carbamic acid 9H-fluoren-9-ylmethyl ester

https://huagongshe.com/de/reaction/12633

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropanolHCID 3776—
Edukt1-((Fmoc)amino)cyclohexanecarboxylic acidHCID 2756093—
EduktBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Edukt2,3-Diaminobenzamide dihydrochlorideHCID 53422807—
LösungsmittelPyridineHCID 1049—
LösungsmittelDimethylformamideHCID 6228—
Produkt[1-(2-Amino-3-carbamoyl-phenylcarbamoyl)-cyclohexyl]-carbamic acid 9H-fluoren-9-ylmethyl esterHCID 68508528—

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

A solution of 1-(9H-fluoren-9-ylmethoxycarbonyl amino)-cyclohexanecarboxylic acid (0.326 g, 0.9 mmol) in pyridine (1 mL) and DMF (1 ml) was heated to 40° C. for 30 min. Carbonyl diimidazole (0.15 g, 0.9 mmol) was added and the mixture was stirred at 40° C. for 1 hour then treated with 2,3-diamino-benzamide dihydrochloride (prepared as described in WO0026192, 0.2 g, 0.9 mmol). After stirring for 1 hour at room temperature, isopropyl alcohol (3 ml) was added and the solution was cooled overnight at 0° C. The precipitated solid was filtered, dissolved in water (3 ml), treated with 50% aqueous NaOH (0.071 ml) then stirred for 3 hours at room temperature. The mixture was filtered and used immediately in Example 48B.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728026B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-3c7f730b94f942349c7865919bff10b4
Quellennotizuspto-grants-2010_06