GUANIDINE COMPOUNDS. II. PREPARATION OF MONO- AND N,N-DI-ALKYLGUANIDINES
1-Guanyl-3,5-dimethylpyrazole nitrate is superior to S-methylisothiouronium sulphate as a reagent for preparation of simple salts of mono- and N,N-di-alkylguanidines from cyclohexylamine, trans-2-aminocyclohexanol, pyrrolidine, and piperidine. S-Methylisothiouronium sulphate, however, gave a higher...
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Veröffentlicht in: | Canadian journal of chemistry 1958-11, Vol.36 (11), p.1541-1549 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | 1-Guanyl-3,5-dimethylpyrazole nitrate is superior to S-methylisothiouronium sulphate as a reagent for preparation of simple salts of mono- and N,N-di-alkylguanidines from cyclohexylamine, trans-2-aminocyclohexanol, pyrrolidine, and piperidine. S-Methylisothiouronium sulphate, however, gave a higher conversion in the case of dimethylamine. Cyanamide is not as useful a guanylating agent as those mentioned above. The paper chromatography of the mono- and N,N-di-alkylguanidines and the parent amines was studied using four solvent systems. |
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ISSN: | 0008-4042 1480-3291 |
DOI: | 10.1139/v58-225 |