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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354178Generated: October 31, 2026

Piperidin-4-ol → HCID 66918845, compound

https://huagongshe.com/reaction/2354178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidin-4-olHCID 79341—
Reactant5-fluoro-N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-2-nitrobenzamideHCID 66918974—
ProductHCID 66918845HCID 66918845—

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 4-hydroxypiperidine was reacted with N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-5-fluoro-2-nitrobenzamide to give N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-5-(4-hydroxypiperidin-1-yl)-2-nitrobenzamide; NMR Spectrum: (DMSOd6) 0.55 (m, 2H), 0.68 (m, 2H), 1.43 (m, 2H), 1.82 (m, 2H), 2.30 (s, 3H), 2.84 (m, 1H), 3.25 (m, 2H), 3.82 (m, 3H), 4.76 (d, 1H), 7.04 (m, 2H), 7.28 (d, 1H), 7.56 (d, 1H), 7.96 (s, 1H), 8.02 (d, 1H), 8.36 (s, 1H), 9.90 (s, 1H); Mass Spectrum: M+Na+ 461.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750154B2
Source datasetuspto-grants-2010_07
ORD IDord-557d74e7719c48a2b0a72e7f33fabf14
Source noteuspto-grants-2010_07