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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248954Generated: November 1, 2026

1,1'-Carbonyldiimidazole → N-[5-[N-[3-(4-chlorophenyl)-3-(2-pyridyl)propyl]-N-methylamino]pentyl]-N'-[3-[3-(piperidinomethyl)phenoxy]propyl]urea

https://huagongshe.com/reaction/248954

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3-(3-(Piperidin-1-ylmethyl)phenoxy)propan-1-amineHCID 10220561—
ReactantHCID 19762500HCID 19762500—
SolventDichloromethaneHCID 6344—
ProductN-[5-[N-[3-(4-chlorophenyl)-3-(2-pyridyl)propyl]-N-methylamino]pentyl]-N'-[3-[3-(piperidinomethyl)phenoxy]propyl]ureaHCID 19762553—

Reaction Steps

Preparation is effected analogously to Example 63, using 1.29 g (3.6 mmol) of N-[3-(4-chlorophenyl)-3-(2-pyridyl)propyl]-N-methyl-1,5-pentanediamine, an equimolar amount of 1,1'-carbonyldiimidazole and 1.04 g (4.2 mmol) of 3-[3-(piperidinomethyl)phenoxy]propaneamine as starting materials. Working up by chromatography (eluant: methylene chloride) analogously to Example 63 yields the purified title compound in the form of an oil; MS (+EI-80 eV): m/z (rel. int.[%])=619 ([M])+.,<1), 230 (17) 203 (100); IR (KBr): 1634 cm-1 (C≡0).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212187
Source datasetuspto-grants-1993_05
ORD IDord-c767768ef986444ea16e61436861b817
Source noteuspto-grants-1993_05