イソヒノリン類の合成研究 (第10報)
ピリヂン核アルキル誘導体の合成 その7
1951 年 71 巻 11 号 p. 1272-1274
詳細
1951 年 71 巻 11 号 p. 1272-1274
Benzyl and anisyl chlorides were respectively condensed with benzyl methyl ketone to yield α, β-diphenyl and α-phenyl-β-(p-methoxyphenyl)-ethyl ketones. Their oximes were reduced, led to amines, condensed with acid amides by the application of acid chloride and submitted to isoquinoline cyclization. Final products were: 1, 3-dimethyl-4-benzyl-, 1-phenyl-3-methyl-4-benzyl-, 1-styryl-3-methyl-4-benzyl- and 1-(3′, 4′, 5′-trimethoxyphenyl)-3-methyl-4-anisyl-3, 4-dihydroisoquinolines.
