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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248972Generated: October 29, 2026

1,1'-Carbonyldiimidazole → HCID 178483546, compound

https://huagongshe.com/reaction/248972

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantN-methyl-N-[3-phenyl-3-(2-pyridyl)propyl]-1,4-butanediamineHCID 19762597—
Reactant2-[4-(2-Aminoethylsulfanylmethyl)-1,3-thiazol-2-yl]guanidineHCID 178512723—
SolventEthylacetate methanolHCID 21584119—
ProductHCID 178483546HCID 178483546—

Reaction Steps

Preparation is effected analogously to Example 63, using 0.89 g (3 mmol) of N-methyl-N-[3-phenyl-3-(2-pyridyl)propyl]-1,4-butanediamine, an equimolar amount of 1,1'-carbonyldiimidazole and 0.75 g (3.2 mmol) of 2-[[(2-guanidino-4-thiazolyl)methyl]thio]ethaneamine as starting materials. Working up by chromatography (eluant: chloroform/methanol 9+1) analogously to Example 63 yields the purified title compound in the form of a dry foam; MS (+FAB method): m/z (rel. int.[%])=555 ([M+H]+ 1), 196 (100); IR (KBr): 1610 cm-1 (C=O). For analytical purposes a sample is converted into the maleic acid salt and recrystallised from ether/ethanol; m.p.: from 80° C. with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212187
Source datasetuspto-grants-1993_05
ORD IDord-88d71ecffe7f48278000d7dd4b22c3ee
Source noteuspto-grants-1993_05