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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248986Generated: October 26, 2026

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

https://huagongshe.com/reaction/248986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-cyano-O-phenyl-N'-[4-[3-(piperidinomethyl)phenoxy]butyl]isoureaHCID 14026191—
ReactantN-[2-[N-(4-fluorobenzyl)-N-(2-pyridyl)amino]ethyl]-N-methyl-1,3-propanediamineHCID 19762569—
ProductN-cyano-N'-[3-[N-[2-[N-(4-fluorobenzyl)-N-(2-pyridyl)amino]ethyl]-N-methylamino]propyl]-N"-[4-[3-(piperidinomethyl)phenoxy]butyl]guanidineHCID 178483801—

Reaction Steps

Preparation is effected analogously to Example 1, using 0.50 g (1.6 mmol) of N-[2-[N-(4-fluorobenzyl)-N-(2-pyridyl)amino]ethyl]-N-methyl-1,3-propanediamine and the equimolar amount of N-cyano-O-phenyl-N'-[4-[3-(piperidinomethyl)phenoxy]butyl]isourea as starting materials. Working up by chromatography analogously to Example 1 yields the purified title compound in the form of a viscous oil; MS (+FAB method): m/z (rel. int. [%])=629 ([M+H]+, 18), 229 (98), 109 (100); IR (KBr): 2164 cm-1 (C≡N). For further analysis, a portion of the compound is converted into the O,O'-ditoluoyltartaric acid salt and recrystallised from isopropanol/ether; m.p.: 102°-105° C. (isopropanol/ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212187
Source datasetuspto-grants-1993_05
ORD IDord-1f48833afe1e433da437afd046e71bb6
Source noteuspto-grants-1993_05