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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 916522Erstellt: 26. Oktober 2026

Diisopropylcarbodiimide → N-alpha-Benzyloxycarbonyl-L-lysine

https://huagongshe.com/reaction/916522

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylcarbodiimideHCID 12734—
EduktCamptothecinHCID 24360—
EduktDicarbobenzoxy-l-lysineHCID 18595285—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-alpha-Benzyloxycarbonyl-L-lysineHCID 75172—

Reaktionsschritte

N,N-Bis CBZ-Lysine (311 mg, 0.75 mmol) was dissolved in 56 mL of anhydrous methylene chloride at room temperature. To this solution were added DIPC (0.12 mL, 0.75 mmol), DMAP (0.61 mg, 0.5 mmol) and camptothecin (0.087 g, 0.25 mmol) at 0° C. The reaction mixture was allowed to warm to room temperature and left for 16 h. The solution was washed with 0.1 N HCl, dried and evaporated under reduced pressure to yield a light yellow solid, which was recrystallized from methanol to give camptothecin-20-ester of N,N-Bis CBZ-Lys 13. Purification of 13 was satisfactory based on TLC and HPLC analysis.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07270808B2
Quelldatensatzuspto-grants-2007_09
ORD IDord-b4763f1fae70488594e09ba58e389690
Quellennotizuspto-grants-2007_09