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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248934Generated: October 30, 2026

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

https://huagongshe.com/reaction/248934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-cyano-O-phenyl-N'-[3-(3-(piperidinomethyl)phenoxy]propyl]isoureaHCID 13486636—
ReactantN-[3-(4-chlorophenyl)-3-(2-pyridyl)propyl]-N-methyl-1,4-butanediamineHCID 19762494—
SolventDichloromethane methanolHCID 21226129—
ProductN-[4-[N-[3-(4-chlorophenyl)-3-(2-pyridyl)propyl]-N-methylamino]butyl]-N'-cyano-N"-[3-[3-(piperidinomethyl)phenoxy]propyl]guanidineHCID 54019736—

Reaction Steps

Preparation is effected analogously to Example 1, using 0.99 g (3 mmol) of N-[3-(4-chlorophenyl)-3-(2-pyridyl)propyl]-N-methyl-1,4-butanediamine and 1.17 g (3 mmol) of N-cyano-O-phenyl-N'-[3-[3-(piperidinomethyl)phenoxy]propyl]isourea as starting materials. Working up by chromatography (eluant: methylene chloride/methanol 98+2) analogously to Example 1 yields the purified title compound in the form of a viscous oil; MS (+FAB method): m/z (rel. int.[%])=630 ([M+H]+, 7), 230 (100); IR (KBr): 2164 cm-1 (C≡N).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212187
Source datasetuspto-grants-1993_05
ORD IDord-1fa1fdc3770148c09795aa988594020b
Source noteuspto-grants-1993_05