HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366412Generated: October 27, 2026
Dicyclohexylcarbodiimide → Deacetylvinblastine 3-aminopropylamide norleucine amide
https://huagongshe.com/reaction/366412
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-tert-Butoxycarbonyl-L-norleucine | HCID 2733747 | — |
| Reactant | Deacetylvinblastine 3-aminopropyl amide | HCID 131721105 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Deacetylvinblastine 3-aminopropylamide norleucine amide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06130204 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-a8ae13aa0ffd462082cbffd406d84937 |
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| Source note | uspto-grants-2000_10 |
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