Process of synthesizing acetylenes disubstituted with a phenyl group and a 2-substituted chromanyl, thiochromanyl or 1,2,3,4-tetrahydroquinolinyl group

Claim 1

A process for synthesizing a compound of the formula (I) ##STR11## where X is S or O; R 1 , R 2 and R 3 are independently hydrogen or lower alkyl; R 4 and R 5 are lower alkyl, with the proviso that R 4 and R 5 are not the same; R 6 is hydrogen, lower alkyl, lower alkenyl or lower cycloalkyl having 1 to 6 carbons or halogen; n is an integer from 0 to 5; B is hydrogen, COOH or a pharmaceutically acceptable salt, ester or amide thereof, --CH 2 OH or an ether or ester derivative thereof, or CHO or an acetal derivative thereof, or --COR" or a ketal derivative thereof where R" is an alkyl, cycloalkyl or alkenyl group containing 1 to 5 carbons, the process comprising the steps of: reacting a compound of formula (II) ##STR12## where R 1 , R 2 and R 3 are defined as above, and Y is halogen when X is S and Y is hydrogen when X is O, with a Gringnard reagent having the formula R 4 --Mg--X' where X' is halogen, to obtain a compound of formula (III) ##STR13## where R 1 , R 2 , R 3 , R 4 , X and Y are defined as above; reacting the compound of formula (III) with a Grignard reagent having the formula R 5 --Mg--X' where R 5 and X' are defined as above, to obtain a compound of formula (IV) ##STR14## where R 1 , R 2 , R 3 , R 4 , R 5 , X and Y are defined as above; converting the compound of formula (IV) to a compound of formula (V) ##STR15## where R 1 , R 2 , R 3 , R 4 , R 5 , X and Y are defined as above; converting the compound of formula (V) into the compound of formula (I), said steps of converting (V) into (I) when X is S including steps of reacting the compound of formula (V) with a trialkylsilylacetylene and thereafter removing the trialkylsilyl group from the product of that reaction under basic conditions to obtain the compound of formula (VI), when X is O said step of converting including steps of reacting the compound of formula (V) with an acetylating agent under Friedel Crafts conditions, and thereafter reacting the product of that reaction with strong base to obtain the compound of formula (VI), said step of converting further including a step of reacting a compound of formula (VI) ##STR16## where R 1 , R 2 , R 3 , R 4 , R 5 and X are defined as above, with a compound of formula (VII) ##STR17## where X' is halogen, and R 6 and n are defined as above.