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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354181Generated: November 3, 2026

Piperidine → N-{5-[(cyclopropylamino)carbonyl)-2-methylphenyl}-2-nitro-5-piperidin-1-ylbenzamide

https://huagongshe.com/reaction/2354181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant5-fluoro-N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-2-nitrobenzamideHCID 66918974—
ProductN-{5-[(cyclopropylamino)carbonyl)-2-methylphenyl}-2-nitro-5-piperidin-1-ylbenzamideHCID 66918911—

Reaction Steps

Using an analogous procedure to that described paragraph (A) in the portion of Example 13 which is concerned with the preparation of starting materials piperidine was reacted with N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-5-fluoro-2-nitrobenzamide to give N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-2-nitro-5-piperidin-1-ylbenzamide; NMR Spectrum: (DMSOd6) 0.56 (m, 2H), 0.68 (m, 2H), 1.60 (m, 6H), 2.30 (s, 3H), 2.82 (m, 1H), 3.52 (m, 4H), 7.02 (m, 2H), 7.27 (d, 1H), 7.55 (d, 1H), 7.96 (s, 1H), 8.02 (d, 1H), 8.39 (s, 1H), 9.95 (s, 1H); Mass Spectrum: M+H+ 423.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750154B2
Source datasetuspto-grants-2010_07
ORD IDord-a79941ae90744133968a24d14788f0f5
Source noteuspto-grants-2010_07