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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040550Generated: October 31, 2026

Piperidine → 4-Amino-4-(1-pyridin-2-yl-cyclopropylcarbamoyl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1040550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant4-(9H-fluoren-9-ylmethoxycarbonylamino)-4-(1-pyridin-2-yl-cyclopropylcarbamoyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 58431236—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-Amino-4-(1-pyridin-2-yl-cyclopropylcarbamoyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 58431060—

Reaction Steps

To the solution of crude 4-(9H-fluoren-9-ylmethoxycarbonylamino)-4-(1-pyridin-2-yl-cyclopropylcarbamoyl)-piperidine-1-carboxylic acid tert-butyl ester in DMF (0.5 mL) was added piperidine (0.2 mL). The mixture was stirred at room temperature. After 1 h, the solution was diluted with EtOAc (20 mL) and washed with water (4×20 mL). The organic phase was dried over anhydrous Na2SO4 and concentrated in vacuo. The resulting residue was purified via flash chromatography on silica gel (10% MeOH in CH2Cl2 containing 0.1% NH4OH) to afford 74 mg of 4-amino-4-(1-pyridin-2-yl-cyclopropylcarbamoyl)-piperidine-1-carboxylic acid tert-butyl ester as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552205B2
Source datasetuspto-grants-2013_10
ORD IDord-6df8efb3ce1e4711a35b73c44a60ef67
Source noteuspto-grants-2013_10