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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916522Generated: October 26, 2026

Diisopropylcarbodiimide → N-alpha-Benzyloxycarbonyl-L-lysine

https://huagongshe.com/reaction/916522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylcarbodiimideHCID 12734—
ReactantCamptothecinHCID 24360—
ReactantDicarbobenzoxy-l-lysineHCID 18595285—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-alpha-Benzyloxycarbonyl-L-lysineHCID 75172—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07270808B2
Source datasetuspto-grants-2007_09
ORD IDord-b4763f1fae70488594e09ba58e389690
Source noteuspto-grants-2007_09