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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606761Generated: October 27, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 4-[1-Phenyl-1-(2-(N-(9-fluorenylmethoxycarbonyl)-3-azetidinecarbonyl)-hydrazinocarbonyl)-methylene]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/606761

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-Fmoc-azetidine-3-carboxylic acidHCID 2756148—
Reactant4-(1-Phenyl-1-hydrazinocarbonyl-methylene)piperidine-1-carboxylic acid tert-butyl esterHCID 11616910—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-[1-Phenyl-1-(2-(N-(9-fluorenylmethoxycarbonyl)-3-azetidinecarbonyl)-hydrazinocarbonyl)-methylene]-piperidine-1-carboxylic acid tert-butyl esterHCID 67046462101.6%

Reaction Steps

To a solution of Fmoc-azetidine-3-carboxylic acid (0.495 g, 1.53 mmol) in CH2Cl2 (10 mL) was added HOBt (0.290 g, 2.14 mmol) and EDCI (0.411 g, 2.14 mmol), and the mixture was allowed to stir for 10 min. To this solution was added 4-(1-phenyl-1-hydrazinocarbonyl-methylene)piperidine-1-carboxylic acid tert-butyl ester (0.507 g, 1.53 mmol), the mixture was stirred for 1 h and then it was diluted with H2O and the layers separated. The aqueous phase was extracted with CH2Cl2 (×3) and the combined organic layers were washed (H2O, brine), dried (Na2SO4) and evaporated to give the title compound (0.99 g, 100%) which was of sufficient purity to be used as such in the following step:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915283B2
Source datasetuspto-grants-2011_03
ORD IDord-18b2ad7bae74419e82b95d5d0c06aaee
Source noteuspto-grants-2011_03