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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354182Generated: October 31, 2026

4-Methylpiperidine → HCID 66918905, compound

https://huagongshe.com/reaction/2354182

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylpiperidineHCID 69381—
Reactant5-fluoro-N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-2-nitrobenzamideHCID 66918974—
ProductHCID 66918905HCID 66918905—

Reaction Steps

Using an analogous procedure to that described in paragraph (A) in the portion of Example 13 which is concerned with the preparation of starting materials 4-methylpiperidine was reacted with N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-5-fluoro-2-nitrobenzamide to give N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-5-(4-methylpiperidin-1-yl)-2-nitrobenzamide; NMR Spectrum: (DMSOd6) 0.56 (m, 2H), 0.66 (m, 2H), 0.92 (d, 3H), 1.13 (m, 2H), 1.68 (m, 3H), 2.30 (s, 3H), 2.83 (m, 1H), 2.99 (t, 2H), 4.07 (d, 2H), 7.03 (m, 2H), 7.28 (d, 1H), 7.56 (d, 1H), 7.96 (s, 1H), 8.01 (d, 1H), 8.39 (s, 1H), 9.95 (s, 1H); Mass Spectrum: M+H+ 437.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750154B2
Source datasetuspto-grants-2010_07
ORD IDord-f07d33bb0b584fdb86c0527e31353155
Source noteuspto-grants-2010_07