Fortschritte Der Arzneimittelforschung / Progress in Drug Research / Progrès Des Recherches Pharmaceutiques 1968
DOI: 10.1007/978-3-0348-7062-7_5
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Die Amidinstruktur in der Arzneistofforschung

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“…For preparation of 2c-e,g,j,m by this method, the products were isolated by distillation and the bases (oil) were converted to crystalline salts. Method C. 2 (2,6-Dimethylbenzyl)-2-imidazoline (4e). A mixture of 2.6-dimethyIphenylacetonitrile16 (2,1 g, 14.5 mmol) and ethvlenediamine mono-p-toluenesulfonate was heated at 190°for 2 hr when the evolution of NH3 ceased (indicated by pH paper).…”
mentioning
confidence: 99%
“…For preparation of 2c-e,g,j,m by this method, the products were isolated by distillation and the bases (oil) were converted to crystalline salts. Method C. 2 (2,6-Dimethylbenzyl)-2-imidazoline (4e). A mixture of 2.6-dimethyIphenylacetonitrile16 (2,1 g, 14.5 mmol) and ethvlenediamine mono-p-toluenesulfonate was heated at 190°for 2 hr when the evolution of NH3 ceased (indicated by pH paper).…”
mentioning
confidence: 99%