Process for preparing 6-chloro-2-chloromethyl-4-phenylquinazoline-3-oxide and intermediates therefor
AssigneePfizer Inc.
InventorsSusumu Nakanishi, Wayne E. Barth
Life of this patent
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Abstract
A process is described for the preparation of 6-chloro-2-chloromethyl-4-phenylquinazoline-3-oxide, a key intermediate in the synthesis of the known useful psychotherapeutic agents: chlorodiazepoxide and diazepam. This intermediate is prepared by the cyclization of 2-(1'-chloroimino-2'-chloromethyl)-5-chlorobenzophenone, itself a new compound. This compound in turn is prepared by the chloroacetylation of 2-amino-5-chlorobenzophenone to 2-chloroacetamido-5-chlorobenzophenone, another novel compound, and subsequent iminochloride formation.
Claims1
A process for preparing 6-chloro-2-chloromethyl-4-phenylquinazoline-3-oxide which comprises the steps of
- a. adding chloroacetyl chloride to a solution under nitrogen atmosphere of 2-amino-5-chlorobenzophenone in methylene chloride, chloroform, benzene or ethyl acetate and 3 N NaOH solution and stirring at 5.degree.-25.degree.C for about 1-4 hours;
- b. separating and contacting the resulting 2-chloroacetamido-5-chlorobenzophenone of step (a) in methylene chloride, chloroform or benzene solvent solution with thionyl chloride, phosgene or phosphorus pentachloride in pyridine under nitrogen atmosphere and heating under reflux;
- and
- c. contacting the resulting crude methylene chloride, chloroform or benzene solvent solution of 2-(1'-chloroimino-2'-chloromethyl)-5-chlorobenzophenone of step (b) with hydroxylamine hydrochloride and pyridine, stirring at 25.degree.- 80.degree.C, pouring reaction mixture into ice-water solution of sodium carbonate, drying the resulting separated methylene chloride, chloroform or benzene layer, concentrating and replacing the methylene chloride, chloroform or benzene with hexane, and collecting formed crystalline 6-chloro-2-chloromethyl-4-phenylquinazoline-3-oxide.
Dependencies are inferred from the claim text.