Abstract A novel process for the synthesis of chiral hydantoins of the structure <IMAGE> (I) wherein X is fluoro or chloro, from the corresponding 6-halo-4-chromanone of the structure <IMAGE> (II) is described. The compounds I are valuable in the treatment of certain chronic complications arising from diabetes mellitus. In addition the compound of the formula I wherein X is chloro possesses complementary hypoglycemic activity. The process comprises the sequence of dehydrative coupling of the halochromanone (II) with S-(-)-alpha-methylbenzylamine to form the imine of structure <IMAGE> (III) addition of hydrogen cyanide to form the nitrile of structure <IMAGE> (IV) condensation with chlorosulfonylisocyanate (or its equivalent) to form the alpha-methylbenzylhydantoin of structure <IMAGE> (V) and finally solvolysis of the latter to the chiral hydantoin of structure I.
The process for preparing a chiral hydantoin of the formula ##STR10## wherein X is chloro or fluoro, from the corresponding halochromanone of the formula ##STR11## which comprises the sequence of dehydrative coupling of the chromanone with S-(-)-alpha-methylbenzylamine to form the imine of the formula ##STR12## adding the elements of hydrogen cyanide to the imine in an anhydrous organic solvent to selectively form and crystallize the chiral nitrile of the formula ##STR13## condensing the nitrile with chlorosulphonyl isocyanate in a reaction-inert solvent, followed by cyclization and hydrolysis in aqueous acid to form the alpha-methylbenzylhydantoin of the formula ##STR14## and solvolyzing the alpha-methylbenzylhydantoin in a strong acid to the chiral hydantoin of formula I.
Claim 2
Dependent Claim
112 words
The process for preparing a chiral hydantoin of the formula ##STR10## wherein X is chloro or fluoro, from the corresponding halochromanone of the formula ##STR11## which comprises the sequence of dehydrative coupling of the chromanone with S-(-)-alpha-methylbenzylamine to form the imine of the formula ##STR12## adding the elements of hydrogen cyanide to the imine in an anhydrous organic solvent to selectively form and crystallize the chiral nitrile of the formula ##STR13## condensing the nitrile with chlorosulphonyl isocyanate in a reaction-inert solvent, followed by cyclization and hydrolysis in aqueous acid to form the alpha-methylbenzylhydantoin of the formula ##STR14## and solvolyzing the alpha-methylbenzylhydantoin in a strong acid to the chiral hydantoin of formula I.
Claim 3
Dependent Claim
9 words
A process of claim 1 wherein X is fluoro.
Claim 4
Dependent Claim
9 words
A process of claim 1 wherein X is chloro.
Claim 5
Dependent Claim
10 words
The compound of the formula ##STR15## wherein X is chloro.
Claim 6
Dependent Claim
10 words
The compound of the formula ##STR15## wherein X is chloro.