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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024702Generated: October 28, 2026

4-(2-Aminoethyl)piperidine, 4-BOC protected → HCID 66818731, compound

https://huagongshe.com/reaction/1024702

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Aminoethyl)piperidine, 4-BOC protectedHCID 1501849—
ReactantHCID 66818161HCID 66818161—
ProductHCID 66818731HCID 6681873169.8%

Reaction Steps

2-(4-cyano phenoxy)-6-(4-trifluoromethoxy phenoxy)nicotinic acid (0.2 g, 0.48 mmol) and (2-Piperidin-4-yl-ethyl)-carbamic acid tert-butyl ester (0.11 g, 0.48 mmol) were coupled using the procedure of Example 5(c) to afford 0.21 g of the required product. Percentage purity (LCMS): 68.11%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722930B2
Source datasetuspto-grants-2014_05
ORD IDord-95e5569b5d6a408a88df5a689d5cfcb0
Source noteuspto-grants-2014_05