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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905653Generated: October 29, 2026

Piperidine → Benzenamine, 4-[4-(1-piperidinyl)butyl]-, hydrochloride (1:2)

https://huagongshe.com/reaction/905653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-(4-Nitrophenyl)butyric acidHCID 79711—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
SolventDimethylformamideHCID 6228—
ProductBenzenamine, 4-[4-(1-piperidinyl)butyl]-, hydrochloride (1:2)HCID 68001600—

Reaction Steps

4-(4-nitrophenyl)butanoic acid and piperidine were allowed to undergo the reaction in DMF using WSC hydrochloride and HOBt, subjected to catalytic hydrogenation in the same manner as shown in Reference Example 3 to reduce the nitro group, and then reduced in the same manner as in Reference Example 2, and the resulting compound was subjected to salt formation using 4 M hydrogen chloride/ethyl acetate solution to obtain 4-(4-piperidin-1-ylbutyl) aniline dihydrochloride. F: 233.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012959B2
Source datasetuspto-grants-2011_09
ORD IDord-f30be38d428d48409a69508d4068b516
Source noteuspto-grants-2011_09