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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024705Generated: October 28, 2026

4-(2-Aminoethyl)piperidine, 4-BOC protected → HCID 66818838, compound

https://huagongshe.com/reaction/1024705

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Aminoethyl)piperidine, 4-BOC protectedHCID 1501849—
ReactantHCID 66818330HCID 66818330—
ProductHCID 66818838HCID 6681883857.1%

Reaction Steps

6-(4-cyano phenoxy)-5-fluoro-2-(3-trifluoromethoxy phenoxy)nicotinic acid (1.3 g, 2.99 mmol) and (2-piperidin-4-yl-ethyl)-carbamic acid tert-butyl ester (0.684 g, 3.0 mmol) were coupled using the procedure of Example 5(c) to afford 1.1 g of the required product. 1HNMR (DMSO-d6): δ 1.2 (2H, m), 1.4 (9H, d), 1.5 (2H, m), 1.6 (2H, m), 2.2 (1H, m), 2.35 (1H, m), 3.0 (3H, m), 3.7 (1H, m), 4.45 (1H, m), 6.78 (1H, m), 7.18 (1H, m), 7.26 (2H, m), 7.32 (1H, s), 7.46 (1H, m), 7.76 (1H, m), 7.86 (1H, s), 8.1 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722930B2
Source datasetuspto-grants-2014_05
ORD IDord-42dde48f318a43a898fb3e95869c75c1
Source noteuspto-grants-2014_05