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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522909Generated: October 31, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 86702793, compound

https://huagongshe.com/reaction/1522909

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
Reactant4-[(chloroacetyl)amino]benzamideHCID 2316688—
SolventAcetonitrileHCID 6342—
ProductHCID 86702793HCID 86702793—

Reaction Steps

A mixture of 4-(2-chloroacetamido)benzamide (0.57 g; 2.68 mmol), tert-butyl piperidin-4-ylcarbamate (0.55 g; 2.68 mmol) and DBU (0.40 mL; 2.68 mmol) in ACN (30 mL) is stirred at r.t. over night. Then the solvent is evaporated and the residue is dissolved in DCM. The solution is washed once with water, then with brine. The organic layer is dried and the solvent is evaporated. The residue is suspended in ether, filtered off with suction and dried to yield tert-butyl 1-(2-(4-carbamoylphenylamino)-2-oxoethyl)piperidin-4-ylcarbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09078909B2
Source datasetuspto-grants-2015_07
ORD IDord-72d54b5a47384f08af933f069dc79c8c
Source noteuspto-grants-2015_07