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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249005Generated: November 1, 2026

N-[2-[N-(4-fluorobenzyl)-N-(2-pyridyl)amino]ethyl]-N-methyl-1,4-butanediamine → HCID 178483536, compound

https://huagongshe.com/reaction/249005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[2-[N-(4-fluorobenzyl)-N-(2-pyridyl)amino]ethyl]-N-methyl-1,4-butanediamineHCID 19762574—
ReactantHCID 178512334HCID 178512334—
ProductHCID 178483536HCID 178483536—

Reaction Steps

Preparation is effected analogously to Example 1, using 0.33 g (1.0 mmol) of N-[2-[N-(4-fluorobenzyl)-N-(2-pyridyl)amino]ethyl]-N-methyl-1,4-butanediamine and the equimolar amount of N-cyano-N'-[2-[[(2-guanidino-4-thiazolyl)methyl]thio]ethyl]-O-phenyl-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. [%])=612 ([M+H]+, 49), 229 (100); IR (KBr): 2165 cm-1 (C≡N). For further analysis, a portion of the compound is converted into the O,O'-ditoluoyltartaric acid salt in an ethanol/ether solvent mixture; m.p.: 137° C. (ethanol/ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212187
Source datasetuspto-grants-1993_05
ORD IDord-796866514d164093875cb721febb8ec2
Source noteuspto-grants-1993_05