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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394440Generated: November 1, 2026

Hydrazinecarboxaldehyde → 4-(1-Phenyl-1-(2-formylhydrazinocarbonyl)-methylene)piperidine-1-carboxylic Acid Tert-Butyl Ester

https://huagongshe.com/reaction/1394440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazinecarboxaldehydeHCID 12229—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-(1-Phenyl-1-carboxy-methylene)piperidine-1-carboxylic acid tert-butyl esterHCID 67046454—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(1-Phenyl-1-(2-formylhydrazinocarbonyl)-methylene)piperidine-1-carboxylic Acid Tert-Butyl EsterHCID 67046375124.4%

Reaction Steps

A mixture of 4-(1-phenyl-1-carboxy-methylene)piperidine-1-carboxylic acid tert-butyl ester (1.05 g, 3.31 mmol), EDCI (0.888 g, 4.63 mmol) and HOBt (0.626 g, 4.63 mmol) in DMF (4 mL) was stirred for 30 min at room temperature and then formic hydrazide (3.97 g, 66.2 mmol) was added. Stirring was continued for 1 h and then the mixture was poured into water and extracted with EtOAc (×3). The combined organic layers were washed (H2O ×3, brine), dried (Na2SO4) and evaporated to give the title compound (1.48 g, 97%) as a colorless oil:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348337B2
Source datasetuspto-grants-2008_03
ORD IDord-103677e0a53844c2b2bcdfa3e37ad66a
Source noteuspto-grants-2008_03