Michne W F, Lewis T R, Michalec S J, Pierson A K, Rosenberg F J
J Med Chem. 1979 Oct;22(10):1158-63. doi: 10.1021/jm00196a002.
A general stereospecific synthesis of (N-methyl-2,6-methano-3-benzazocin-11 beta-yl)alkanones is described and applied to the preparation of a series of alkyl ketones wherein the alkyl group is a straight or terminally branched chain containing from one to six carbon atoms. Several compounds with methoxy groups in the aromatic ring are in the morphine range of potency; they are uniformly inactive as phenazocine antagonists. Phenolic analogues range up to 100 times as potent as morphine. Those containing five or six carbon atoms in the alkyl group exhibit phenazocine antagonist activity, in one case equivalent to naloxone. This compound (3e) is selective for phenazocine in its antagonist action.
描述了一种通用的立体定向合成(N-甲基-2,6-亚甲基-3-苯并氮杂环辛-11β-基)链烷酮的方法,并将其应用于制备一系列烷基酮,其中烷基为含有1至6个碳原子的直链或末端支链。芳香环中带有甲氧基的几种化合物具有吗啡范围内的效力;它们作为非那佐辛拮抗剂均无活性。酚类类似物的效力比吗啡高100倍。烷基中含有五个或六个碳原子的那些化合物表现出非那佐辛拮抗剂活性,在一种情况下与纳洛酮相当。该化合物(3e)在其拮抗作用中对非那佐辛具有选择性。