Synthesis of heterocycles-1. One step synthesis of acetylthiadiazolines
โ Scribed by N.F. Eweiss; A. Osman
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- French
- Weight
- 108 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
The 5-imino-A2-1,3,4_thiadiazolines reported sofar' were prepared from hydrazidic halides and thiourea or KSCN. The preparation of the hydrazidic halides is limited to either the reaction of a hydrazide with PC15 or the halogenation of an aldehydic hydrazone2. In this communication we wish to report an efficient one step synthesis of 2-acetyl-4-aryl-5-imino-A2-1,3,4thiadiazolines (1 a-e) from (2) and aryldiazonium chlorides. No syntheses of
๐ SIMILAR VOLUMES
Dimerizations of cyclic enamines 1 (R=H2) occurring via iminium intermediates 2 (R=H2) are well-known 1) and have been applied recently in alkaloid synthe-sis2). Schematically the overall process can be represented as follows: R'
## Abstract For Abstract see ChemInform Abstract in Full Text.
Five naturally occurring bases with an oxasole ring have been known to date, all bearing substituent at 2 and 5 position l-4) and because of their relatively