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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105304Generated: November 2, 2026

4-Nitrophenol → 4-(1-Methylpiperidin-3-ylmethoxy)-phenylamine

https://huagongshe.com/reaction/2105304

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
Reactant3-(Chloromethyl)-1-methylpiperidineHCID 103674—
Product4-(1-Methylpiperidin-3-ylmethoxy)-phenylamineHCID 21974798—

Reaction Steps

Using the procedure of Example 56, 4-nitro-phenol Compound 104a was used in place of Compound 36a and 3-chloromethyl-1-methyl-piperidine Compound 104b was used in place of Compound 56a and carried forward to provide 4-(1-methyl-piperidin-3-ylmethoxy)-phenylamine Compound 104d. MS 221 (MH+). Using the procedure of Example 1, 5-(2,4-dichloro-phenyl)-4-oxo-4,5-dihydro-3H-1-thia-3,5,6,8-tetraaza-acenaphthylene-2-carboxylic acid Compound 43c was used in place of Compound 1 and Compound 104d was used in place of 4-piperidin-1-ylmethyl-phenylamine Compound 1k to give Compound 32. MS 583, 585, 587 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579356B2
Source datasetuspto-grants-2009_08
ORD IDord-a8545058cabc466783da993ca6b580ea
Source noteuspto-grants-2009_08