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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305357Generated: November 2, 2026

1,1'-Carbonyldiimidazole → HCID 10550636, compound

https://huagongshe.com/reaction/2305357

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant1-Carbobenzoxy-4-piperidinecarboxylic AcidHCID 736489—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10550636HCID 1055063689.3%

Reaction Steps

To a solution of N-benzyloxycarbonyl isonipecotic acid (123.64 g) in tetrahydrofuran (300 ml) at 0° C. was added a solution of carbonyldiimidazole (68.80 g) in tetrahydrofuran (500 ml) and dichloromethane (300 ml). The resulting solution was stirred at ambient temperature for 2 hours. This solution was cooled to 0° C. and a solution of 1-(tert-butoxycarbonyl)piperazine (87.02 g) in tetrahydrofuran (200 ml) added dropwise over minutes. The suspension obtained was stirred at ambient temperature for 48 hours. Solvent was evaporated. The residue was dissolved in diethyl ether/dichloromethane (1500 ml) and washed with water, 2M aqueous citric acid solution, saturated aqueous sodium bicarbonate solution, dried (Na2SO4) and evaporated to give 1-(tert-butoxycarbonyl)-4-[1-benzyloxycarbonylpiperidin-4-ylcarbonyl]piperazine (180.00 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06440972B1
Source datasetuspto-grants-2002_08
ORD IDord-7565467ff95b4deb8b15391aef079e30
Source noteuspto-grants-2002_08