✦ LIBER ✦

Olefinic Derivatives of 2,4-Diamino-s-triazines

✍ Scribed by LUSKIN, LEO S.; BENNEVILLE, PETER L. DE; MELAMED, SIDNEY

Book ID: 120734181
Publisher: American Chemical Society
Year: 1958
Tongue: English
Weight: 631 KB
Volume: 23
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo01101a026

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Exploration of 2, 4-diaminopyrimidine an

Exploration of 2, 4-diaminopyrimidine and 2, 4-diamino-s-triazine derivatives as potential antifilarial agents

✍ SHARMA, R. D.; BAG, S.; TAWARI, N. R.; DEGANI, M. S.; GOSWAMI, K.; REDDY, M. V. 📂 Article 📅 2013 🏛 Cambridge University Press 🌐 English ⚖ 341 KB

A facile one pot synthesis of 2, 4-diami

A facile one pot synthesis of 2, 4-diamino-6-substituted s-triazine derivatives

✍ Ramadas Sathunuru; Victor Melendez; Michael P. Kozar; Ai J. Lin 📂 Article 📅 2008 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 269 KB 👁 1 views

## Abstract magnified image A novel and facile one‐pot procedure for the preparation of 2,4‐diamino‐6‐substituted‐s‐triazine derivatives (IIa‐n) was reported. The scope of its application was demonstrated with a number of examples. The new procedure involved treatment of proguanil or chloroproguan

4,6-Diamino-1-alkyl-1,2-dihydro-s-triazi

4,6-Diamino-1-alkyl-1,2-dihydro-s-triazines

✍ Lombardino, Joseph G. 📂 Article 📅 1963 🏛 American Chemical Society 🌐 English ⚖ 259 KB

Synthesis and characterization of 2-urey

Synthesis and characterization of 2-ureylene-4,6-diamino-s-triazines

✍ Herweh, John E.; Whitmore, William Y. 📂 Article 📅 1970 🏛 American Chemical Society 🌐 English ⚖ 376 KB

Triazine isocyanates: Part II: Reaction

Triazine isocyanates: Part II: Reaction of 2,4-diamino-s-triazines with ethyl chlorocarbonate

✍ E. F. J. Duynstee; Th. Veerkamp 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 504 KB

## Abstract Benzoguanamine (2,4‐diamino‐6‐phenyl‐s‐triazine) and acetoguanamine (2,4‐diamino‐6‐methyl‐s‐triazine) both react with an excess of ethyl chlorocarbonate; in this reaction two hydrogen atoms from the guanamines are replaced by two carbethoxy groups. The I.R. spectrum reveals that this do

Preparation of 2,4-diamino-6-(diallylami

Preparation of 2,4-diamino-6-(diallylamino)-s-triazine-2,4-14c and its hypotensive metabolite, 2,4-diamino-6-(diallylamino)-s-triazine-2,4-14c 3-oxide

✍ Richard C. Thomas 📂 Article 📅 1978 🏛 John Wiley and Sons 🌐 French ⚖ 202 KB

## Abstract 2,4‐Diamino‐6‐(diallylamino)‐__s__‐triazine‐2,4‐^14^C was prepared from K^14^CN in a four step sequence of reactions. The product was obtained in 26% yield at a specific activity of 1.01 mCi per mM. This product was converted to the hypotensive agent, 2,4‐diamino‐6‐(diallylamino)‐__s__‐