Hydroxy benzamide

Hydrogen-bond-based strategies have also been successfully employed in the supramolecular assembly of metal clusters. The reaction of [Mo6C18]4+ ions with six equivalents of 4-hydroxy-benzamide yielded six octahedrally arranged oxobenzamide groups per cluster. Amide- amide hydrogen bonds produced infinite 2D networks separated by counterions.57... 

Pentxhloro-2 -hydroxysalicylanilide Salicylanilide. 3,3 ,5,5, 6-pentachloro-2 -hydroxy- 2,3,5Trichloro-N-(3,5-dichloro-2-hydroxyphenyl)-6-hydroxy-benzamide Zanil Zanilox. A vetrinary anthelmintic (Trematodes). Used in combination with Haloxon. Solid mp = 209-211°. 

Synonyms. 5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxy-benzamide 5-Chloro-salicyloyl-(o-chloro-p-nitranilide) N-(2 -Chloro-4 -nitrophenyl)-5-chlorosalicylamide. 

Synonyms 3,5-Dichloro-N-(3,4-dichlorophenyl)-2-hydroxy benzamide 3,3, 4, 5-Tetrachlorosalicylanilide... 

Diazepines have attracted considerable attention in 1980, as befits their commercial importance as antidepressents and in other medicinal applications. Work appeared from Roche describing further investigations into the industrial preparation of the antidepressants, and another group prepared a pyrrolo-benzo[l,4]diazepinone in an analogous manner.Possibly of more interest were two reports on the preparation of 1,3-diazepines which are not so common. Ishikawa et reported the synthesis of (424) by standard methods, and Coyle etal produced (426) by acid-catalysed cyclodehydration of the hydroxy-benzamide (425) in >80% yield. Phthalimide Mannich bases have been widely investigated by several groups in analogous conversions as discussed earlier. 

Butyl-4-chloro-2-hydroxy- benzamide Buclosamide C H,4CIN02 575-74-6 227.688 91.5 ... 

Cyclopropanols 72 are obtained in amazingly good yields (up to 70%) when air (or oxygen) is bubbled into ethereal solutions of cyclopropyllithiums (Scheme 1-50). or / o-Lithiated jV.A-diethylbenzamides, O-lithio benzylalcoholate, and 4-(4,4-dimethyl-2-oxazolin-2-yl)pyridine afford 2-hydroxy-benzamides 73 (Scheme 1-50), 2-(hydroxymethyl)phenol, and 3-hydroxypyridine in moderate yields (25 50%). 

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