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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782008Generated: October 28, 2026

4-(N-Boc-amino)piperidine → {1-[2-(6-Cyano-quinolin-4-yl)-ethyl]-piperidin-4-yl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1782008

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(N-Boc-amino)piperidineHCID 723833—
Reactant4-Vinyl-quinoline-6-carbonitrileHCID 11492040—
SolventChloroformHCID 6212—
Product{1-[2-(6-Cyano-quinolin-4-yl)-ethyl]-piperidin-4-yl}-carbamic acid tert-butyl esterHCID 1157445399.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of (d) (150 mg, 0.8 mmol), piperidin-4-yl-carbamic acid tert-butyl ester (166 mg, 0.8 mmol) and chloroform (0.5 ml) were heated at 50° C. in a loosely capped vial for 6 hours. The product was purified by flash silica chromatography eluting with a 0-2% methanol in chloroform gradient affording the product as a foam (304 mg, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498326B2
Source datasetuspto-grants-2009_03
ORD IDord-281727cb74e9404f8ec80ef3f0e73d68
Source noteuspto-grants-2009_03