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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11863Erstellt: 25. Oktober 2026

4-((((Benzyloxy)carbonyl)amino)methyl)benzoic acid → HCID 86592268, Verbindung

https://huagongshe.com/reaction/11863

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-((((Benzyloxy)carbonyl)amino)methyl)benzoic acidHCID 1479997—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Edukt(2S)-2-amino-5-(((tert-butoxy)carbonyl)amino)pentanoic acidHCID 6993436—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDimethylformamideHCID 6228—
ProduktHydrochloric AcidHCID 313—
ProduktHCID 86592268HCID 8659226838%

Reaktionsschritte

The compound obtained in Example 23-2 (350 mg) was dissolved in DMF (7 ml). After the addition of WSCI hydrochloride (265.0 g), DMAP (169 mg), and the compound obtained in Example 41-1 (276.0 mg), the mixture was stirred for 24 hours at room temperature. After the reaction, the solvent was removed by distillation. The residue was dissolved in chloroform, washed with 1 mol/l aqueous solution of hydrochloric acid and saturated aqueous solution of sodium hydrogencarbonate, and dried over sodium hydrogensulfate. The solvent was removed by distillation and the residue was purified by silica gel column chromatography (20 g, chloroform/methanol=10/1). 130 mg of the obtained product was dissolved in methanol (2.6 ml) and 4 mol/l hydrochloric acid/dioxane solution (2.6 ml) was added. The mixture was stirred for 70 minutes at room temperature. After the reaction, the solvent was removed by distillation and the residue was dried under vacuum to obtain hydrochloride of the title compound (147 mg) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07098215B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-447f2211d39544d9a51ee1929e302857
Quellennotizuspto-grants-2006_08