Ethanol → 2-[1-(2-Hydroxyethyl)-2-imidazolidinyl-idene]-aminobiphenyl fumarate

HRID 1464036Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1464036
I.[C:2]1([C:13]2C=CC=CC=2)[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[NH:8]C(=N)SC.[OH:19][CH2:20][CH2:21][NH:22][CH2:23][CH2:24][NH2:25].[C:26]([OH:33])(=[O:32])/[CH:27]=[CH:28]/[C:29]([OH:31])=[O:30].[CH2:34](O)[CH3:35]>CO>[C:26]([OH:33])(=[O:32])/[CH:27]=[CH:28]/[C:29]([OH:31])=[O:30].[OH:19][CH2:20][CH2:21][N:22]1[CH2:23][CH2:24][NH:25][C:13]1=[C:2]1[CH:3]([NH2:8])[CH:4]=[CH:5][CH:6]=[C:7]1[C:35]1[CH:34]=[CH:29][CH:28]=[CH:27][CH:26]=1

Komponenten

6

Versuchsvorschrift

A mixture of 1-(2-biphenylyl)-2-methyl-2-thiopseudourea hydriodide (12 g prepared as described in Example 5) and N-(2-hydroxyethyl)ethylenediamine (10 g) in ethanol (145 ml) was heated under reflux for 165 hours. Removal of the solvent gave an oil which was dissolved in methanol and treated with fumaric acid to give 2-[1-(2-hydroxyethyl)-2-imidazolidinyl-idene]-aminobiphenyl fumarate (m.p. 165°-166° C.) which was recrystallised from a 1:2 mixture of methanol and ether.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureunder reflux for 165 hours
  3. customRemoval of the solvent
  4. customgave an oil which

Quellen und Nachweise

ORD-Eintrag
ord-7676d414f45440c9b06f6714e0dd189a
Quelldatensatz
uspto-grants-1994_04
Patentnummer
US05302720

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