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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248935Generated: October 29, 2026

N-cyano-O-phenyl-N'-[3-(3-(piperidinomethyl)phenoxy]propyl]isourea → N-[3-[N-[3-(4-chlorophenyl)-3-(2-pyridyl)propyl]-N-methylamino]-propyl]-N'-cyano-N"-[3-[3-(piperidinomethyl)phenoxy]propyl]guanidine

https://huagongshe.com/reaction/248935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-cyano-O-phenyl-N'-[3-(3-(piperidinomethyl)phenoxy]propyl]isoureaHCID 13486636—
ReactantHCID 19762536HCID 19762536—
SolventEthyl AcetateHCID 8857—
ProductN-[3-[N-[3-(4-chlorophenyl)-3-(2-pyridyl)propyl]-N-methylamino]-propyl]-N'-cyano-N"-[3-[3-(piperidinomethyl)phenoxy]propyl]guanidineHCID 53960905—

Reaction Steps

Preparation is effected analogously to Example 1, using 0.5 g (1.57 mmol) of N-[3-(4-chlorophenyl)-3-(2-pyridyl)propyl]-N-methyl-1,3-propanediamine and 0.6 g (1.5 mmol) of N-cyano-O-phenyl-N'-[3-[3-(piperidinomethyl)phenoxy]propyl]isourea as starting materials. Working up by chromatography (eluant: ethyl acetate) analogously to Example 1 yields the purified title compound in the form of a viscous oil; MS (+FAB method): m/z (rel. int.[%])=616 ([M+H]+, 1), 230 (100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212187
Source datasetuspto-grants-1993_05
ORD IDord-6211fe558b44411ca5c2d2e335eb9044
Source noteuspto-grants-1993_05