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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115108Generated: October 27, 2026

4-(Methyl-p-tolyl-amino)-piperidine → 1-Piperidineacetamide,4-[methyl(4-methylphenyl)amino]-n-[4-[(methylsulfonyl)amino]phenyl]-

https://huagongshe.com/reaction/2115108

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Methyl-p-tolyl-amino)-piperidineHCID 61981015—
Reactant1-Piperidineacetamide,n-[4-[(methylsulfonyl)amino]phenyl]-4-(phenylmethyl)-HCID 69099975—
SolventDiethyl EtherHCID 3283—
Product1-Piperidineacetamide,4-[methyl(4-methylphenyl)amino]-n-[4-[(methylsulfonyl)amino]phenyl]-HCID 69101010—

Reaction Steps

The title compound is prepared from 2-chloro-N-(4-methanesulfonylamino-phenyl)-acetamide (Example 180) and 4-(methyl-p-tolyl-amino)-piperidine [Arzneimittel Forschung/Drug Research 44(II), 989. (19994)]) according to the method described in Example 142b. Melting Point: 128-130° C. (diethylether)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435744B2
Source datasetuspto-grants-2008_10
ORD IDord-92ad52f871c54b6499ca851957b17b87
Source noteuspto-grants-2008_10