Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248967Generated: October 29, 2026

1,1'-Carbonyldiimidazole → N-[3-[N-[3-(4-chlorophenyl)-3-(2-pyridyl)propyl]-N-methylamino]propyl]-N'-[2-[[(2-guanidino-4-thiazolyl)methyl]thio]ethyl]urea

https://huagongshe.com/reaction/248967

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 19762536HCID 19762536—
Reactant2-[4-(2-Aminoethylsulfanylmethyl)-1,3-thiazol-2-yl]guanidineHCID 178512723—
SolventEthylacetate methanolHCID 21584119—
ProductN-[3-[N-[3-(4-chlorophenyl)-3-(2-pyridyl)propyl]-N-methylamino]propyl]-N'-[2-[[(2-guanidino-4-thiazolyl)methyl]thio]ethyl]ureaHCID 178483844—

Reaction Steps

Preparation is effected analogously to Example 63, using 0.9 g (2.8 mmol) of N-[3-(4-chlorophenyl)-3-(2-pyridyl)propyl]-N-methyl-1,3-propanediamine, an equimolar amount of 1,1'-carbonyldiimidazole and 0.73 g (3.1 mmol) of 2-[[(2-guanidino-4-thiazolyl)methyl]thio]ethaneamine as starting materials. Working up by chromatography (eluant: ethyl acetate/methanol 85+15) analogously to Example 63 yields the purified title compound in the form of a dry foam; MS (+FAB method): m/z (rel. int.[%])=575 ([M+H]+, 3), 155 (22), 230 (100); IR (KBr): 1646 cm-1 (C=O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212187
Source datasetuspto-grants-1993_05
ORD IDord-fb5ea7fca4c141238f69eaaf692f6037
Source noteuspto-grants-1993_05