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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366412Generated: October 27, 2026

Dicyclohexylcarbodiimide → Deacetylvinblastine 3-aminopropylamide norleucine amide

https://huagongshe.com/reaction/366412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-tert-Butoxycarbonyl-L-norleucineHCID 2733747—
ReactantDeacetylvinblastine 3-aminopropyl amideHCID 131721105—
SolventDimethylformamideHCID 6228—
ProductDeacetylvinblastine 3-aminopropylamide norleucine amideHCID 131722119—

Reaction Steps

To a DMF solution (1 ml) of Boc-Nle (22 mg, 0.095 mmol) was added 318 μl of a 1M solution of HOBT (in NMP) followed by 280 μl of a 1M solution of DCC (in NMP). After 30 min., intermediate (11) (0.0624 mmol) was added in a 3.5 ml DMF. The pH of the reaction was adjusted ~7.5 with diisopropylethylamine. After stirring for 18 hrs the reaction was concentrated to an oil and the Boc protecting group removed by treating the oil with a 1:1 solution of TFA: CH2Cl2 (20 ml). After 5 min. the reaction was concentrated to dryness. Purification was achieved by preparative HPLC on a C-18 reverse phase support (Waters, Delta Pak). Buffer A=0.1% TFA-H2O; B=0.1% TFA-CH3CN. The crude product was loaded in 100% A buffer (100 ml) and a step gradient of 100% A to 30% A was used at a flow rate of 75 ml/min. Homogeneous product fractions were pooled and freeze-dried to yield (12).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130204
Source datasetuspto-grants-2000_10
ORD IDord-a8ae13aa0ffd462082cbffd406d84937
Source noteuspto-grants-2000_10