A method of preparation for the title compounds 5, by bromination-dehydrobromination of the corresponding 5-alkyl-1,2,3-thiadiazoles 3, their spectroscopical characterization, and the reaction of 5 with 4-phenyl-4H-l,2,4-triazole-3,5-dione (6) with formation of 7, 8 is described. 1,2,3-Thiadiazole
Bicyclic thiadiazoles I: 2-(2-thienyl)-5-phenylthiazolo[2,3-b]-1,3,4-thiadiazole
β Scribed by Man M. Kochhar; Mohammad Salahi-Asbahi; Byron B. Williams
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- English
- Weight
- 216 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0022-3549
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β¦ Synopsis
hydrates could be air milled, the author proceeded to pnpare suspensions with air-milled hydrate to see if crystal growth still oe curted. Work was done with I-hydrate, because at that time development work on 11 had been discontinued. A 2.5% suspension of air-milled I-hydrate was made (Table ) and observed for 2 years by microscopic examination and particle-size analysis. No evidetice for crystal growth was observed.
This case history shows that suspensions are dynamic systems and that it is important to establish which forms are present at equilibrium. It shows that careful work is needed to identify these forms and prove that they can be processed to specifications prior to suspension formulation work. In addition, this report shows that satisfactory suspensions can be made with these equilibrium form.
π SIMILAR VOLUMES
From the title compound 1 and KF in sulfolane 3-chloro-4-fluoro-(2) and 3,4-difluoro-I ,2,5-thiadiazole (3) are obtained. In the reaction with oxidizing fluorinating agents, e. g. XeF,, BrF,, or AgF,, 2 is the primary product. Cleavage of the ring system at one of the S = N bonds gives the bifunctio