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
Hauptverfasser: Bannard, R. A. B, Casselman, A. A, Cockburn, W. F, Brown, G. M
Format: Artikel
Sprache:eng
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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.
ISSN:0008-4042
1480-3291
DOI:10.1139/v58-225