Benzyl cyanide Tolazoline

Benzyl chlorocarbonate Ampicillin Benzyl cyanide Meperidine HCI Tolazoline... [Pg.1616]

The reaction between a mole each of benzyl cyanide and ethylene diamine in the presence of carbon disulphide as a medium gives rise to the formation of the desired tolazoline (base) through cyclization and subsequent elimination of a mole each of hydrogen sulphide and ammonia that are liberated from the reaction mixture. The base thus obtained is treated with a HCl in molar concentration to obtain the corresponding salt. [Pg.390]

Benzethonium chloride Benzphetamine HCI Bephenium hydroxynaphthoate Bufeniode Oiazoxide Ifenprodil tartrate Phenoxybenzamine HCI Propoxyphene HCI Tiopronin Tribenoside Benzyl chlorocarbonate Ampicillin Benzyl cyanide Meperidine HCI Tolazoline... [Pg.1616]

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