Thiazole Analogs of Benzomorphans. III. Syntheses of 4, 5, 6, 7, 8, 9-Hexahydro-4, 8-methano-5-methylthiazolo [4, 5-c] azocine and 4, 5, 6, 7, 8, 9-Hexahydro-4, 8-methano-5-methylthiazolo [5, 4-c] azocine

抄録

Syntheses of 4, 5, 6, 7, 8, 9-hexahydro-4, 8-methano-5-methylthiazolo [4, 5-c] azocine (III) and 4, 5, 6, 7, 8, 9-hexahydro-4, 8-methano-5-methylthiazolo [5, 4-c] azocine (IV) are described. Thiazolization of 2-azabicyclo [3. 3. 1] nonan-8-one (V) gave the 2-aminothiazole (VII), which was converted into III by deamination, hydrolysis of the benzoyl group and Esch-weiler-Clarke N-methylation. The 2-hydroxyl derivative (XIII) was also synthesized. On the other hand, compound (IV) was synthesized by cyclization of the olefinic urethane (XXI) with phenylselenenyl chloride, as a key step. Deselenation of XXII with triphenyltin hydride followed by LiAlH₄ reduction gave IV. The urethane (XXI) was prepared from the 2-aminothiazole (XVIIa), which was obtained by condensation of the bromodiketone (XVI) and thiourea.