Process for producing 5-substituted oxazole compounds and 5-substituted imidazole compounds

Abstract

A process for producing heterocyclic compounds which are useful as pesticides, drugs, fungicidal materials or intermediates thereof. TosMIC is reacted with an aldehyde or an imino compound: 1) in a solvent mixture of an aprotic solvent with a protic solvent in the presence of a base, 2) in the presence of a phase-transfer catalyst and an inorganic base, or 3) in the presence of an inorganic base. Thus, a desired product can be efficiently obtained using a solution without isolating TosMIC which is irritating and unstable, has a low decomposition point and shows explosivity.

1 . A process for the preparation of a 5-substituted oxazole or 5-substituted imidazole comprising 
 synthesizing p-tolylsulfonylmethylisocyanide from N-(p-tolylsulfonylmethyl)formamide with phosphorus oxychloride, phosgene or diphosgene, and a tertiary amine, to form a p-tolylsulfonylmethylisocyanide solution which is not isolated and purified as crystals, and    reacting the p-tolylsulfonylmethylisocyanide solution with an aldehyde or a compound represented by Formula (I):      R 1 CH═NR 2    wherein, R 1  and R 2  are each independently an optionally substituted phenyl, an optionally substituted heterocyclic group or an optionally substituted alkyl,      wherein the p-tolylsulfonylmethylisocyanide solution is reacted with an aldehyde or a compound of Formula (I) in a mixed solvent of an aprotic solvent and a protic solvent in the presence of potassium hydroxide or sodium hydroxide or mixtures thereof.    
   
   
       2 . (canceled)  
   
   
       3 . A process according to  claim 1  in which the protic solvent is one or more solvents selected from the group consisting of water, C 1  to C 10  alcohols and mono- or poly-alkylene glycols.  
   
   
       4 . A process for the preparation of a 5-substituted oxazole or 5-substituted imidazole comprising 
 synthesizing p-tolylsulfonylmethylisocyanide from N-(p-tolylsulfonylmethyl) formamide with phosphorus oxychloride, phosgene or diphosgene, and a tertiary amine, to form a p-tolylsulfonylmethylisocyanide solution which is not isolated and purified as crystals, and    reacting the p-tolylsulfonylmethylisocyanide solution with an aldehyde or a compound represented by Formula (I):      R 1 CH═NR 2    wherein R 1  and R 2  are each independently an optionally substituted phenyl, an optionally substituted heterocyclic group or an optionally substituted alkyl,      wherein the aldehyde or the compound of Formula [I] is reacted with p-tolylsulfonylmethylisocyanide in a mixed solvent of an aprotic solvent and water in the presence of between about 0.0001 moles and about 5 moles of at least one phase-transfer catalyst and an inorganic base.    
   
   
       5 . A process for the preparation of a 5-substituted oxazole or 5-substituted imidazole comprising 
 synthesizing p-tolylsulfonylmethylisocyanide from N-(p-tolylsulfonylmethyl) formamide with phosphorus oxychloride, phosgene or diphosgene, and a tertiary amine, to form a p-tolylsulfonylmethylisocyanide solution which is not isolated and purified as crystals, and    reacting the p-tolylsulfonylmethylisocyanide solution with an aldehyde or a compound represented by Formula (I):      R 1 CH═NR 2    wherein R 1  and R 2  are each independently an optionally substituted phenyl, an optionally substituted heterocyclic group or an optionally substituted alkyl,      wherein the aldehyde or the compound of Formula [I] is reacted with p-tolylsulfonylmethylisocyanide in the presence of an organic base which has a pKa of 12 or more.    
   
   
       6 . (canceled)  
   
   
       7 . The process according to  claim 5 , wherein the organic base is 1,8-diazabicyclo[5.4.0]undec-7-ene or 4-(N,N-dimethylamino)pyridine.  
   
   
       8 . The process according to  claim 1 , wherein the aldehyde is an unsubstituted or substituted aromatic aldehyde.  
   
   
       9 - 11 . (canceled)  
   
   
       12 . The process according to  claim 4  wherein the aldehyde is an unsubstituted or substituted aromatic aldehyde.  
   
   
       13 . The process according to  claim 5  wherein the aldehyde is an unsubstituted or substituted aromatic aldehyde.  
   
   
       14 . The process according to  claim 4 , wherein the phase transfer catalyst is at least one phase transfer catalyst selected from the group consisting of quaternary ammonium salts, quaternary phosphonium salts, crown compounds and organic bases.