An alternative route to 2H-naphtho[1,2-b]thiete and its cycloaddition products

2-(1H-Benzotriazol-1-ylmethyl)-1-naphthalenol ( 1 ) can be transformed in high yields to the corresponding thiol 4 . Flash vacuum pyrolysis of 4 leads to 2H-naphtho[1,2-b]thiete ( 5 ). The benzotriazolyl group proved to be a good leaving group; however, a subsequent nitrogen extrusion takes place under flash vacuum pyrolysis conditions and cyclopentadienecarbonitriles 6a,b are formed by a ring contraction (Scheme 1). Cycloaddition reactions of 5 and dienophiles or heterodienophiles yield the naphtho-condensed sulfur heterocycles 8, 10, 12 and 14 (Scheme 2).