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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867688Generated: November 1, 2026

1-Benzyl-4-(methylamino)piperidine-4-carboxamide → 4-(Methylamino)piperidine-4-carboxamide

https://huagongshe.com/reaction/1867688

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(methylamino)piperidine-4-carboxamideHCID 96411—
ReactantHCID 23541247HCID 23541247—
Product4-(Methylamino)piperidine-4-carboxamideHCID 96474—

Reaction Steps

The 1-isopropyl-4-(methylamino)piperidine-4-carboxamide used as starting material was prepared as follows: 1-benzyl-4-(methylamino)piperidine-4-carboxamide (J Med Chem., 1998, 41(25), 5084) may be deprotected by hydrogenation using an analogous method to that described for the equivalent step in Example 74 to give 4-(methylamino)piperidine-4-carboxamide; 1H NMR Spectrum: 1.35 (m, 2H); 1.68 (m, 2H); 1.93 (brs, 1H); 2.06 (s, 3H), 2.59 (m, 2H); 2.71 (m, 2H); 6.81 (s, 1H); 7.14 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632840B2
Source datasetuspto-grants-2009_12
ORD IDord-6d666387f56c43278fd1d44162059019
Source noteuspto-grants-2009_12