pyridines 4a-e was prepared by the reaction of 5-ethylthio-1,3,4-thiadiazole-2-amine (1) and p-substituted 3-(dimeth-1,3,4-Thiadiazoles find a variety of applications as antibiotic, antiinflammatory or bacteriostatic agents and as pesticides [1] [2] . These biological activities have stimulated us t
1-Alkyl- and Azeto[1,2-a][1,5]benzodiazepine Derivatives in the Reaction of o-Phenylenediamine with 3-(Dimethylamino)propiophenones
β Scribed by Braulio Insuasty; Rodrigo Abonia; Jairo Quiroga; Angela Salcedo; Heinz Kolshorn; Herbert Meier
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 252 KB
- Volume
- 2000
- Category
- Article
- ISSN
- 1434-193X
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β¦ Synopsis
1,5-benzodiazepines / Cyclizations / Cycloadditions
The reaction of o-phenylenediamine (4) with one, two or three equivalents of p-substituted 3-dimethylaminopropiophenone hydrochlorides 5a-e was studied. 4-Aryl-2,3-dihydro-1H-1,5-benzodiazepine derivatives 6a-e were obtained in good yields, along with the 1:2-adducts 7c-e and
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S-Arsenic(III) and arsenic(V) derivatives of aryldithiophosphonic, aryltrithiophosphonite, and aryl(amido)dithiophosphonic acids 3a-c, 5, 7, and 9a-c were obtained by the reactions of 2,4-diaryl-1,3,2,4-dithiadiphosphetane-2,4-disulfides 1a,b with O-isobutyl arsinite 2a, O,O-dimethylphosphonites 2b,
A small variation in the vanadium reagent leads to a completely different product: The cyclooligomerization of phosphaalkynes 2 with tBuN=VCl β DME (DME=1,2-dimethoxyethane) proceeds with incorporation of the imido fragment to give the azatetraphosphaquadricyclanes 1. In contrast, with the correspond