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【结 构 式】

【分子编号】26921

【品名】(1S,4aS,10aR)-6-hydroxy-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydro-1-phenanthrenecarboxylic acid

【CA登记号】5947-49-9

【 分 子 式 】C17H22O3

【 分 子 量 】274.35988

【元素组成】C 74.42% H 8.08% O 17.49%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(I)

The methylation of podocarpic acid (I) (J Org Chem 1974, 39: 1968) gives methyl O-methylpodocarpate (II), which is oxidized with CrO3 in acetic acid.

1 Hornback, W.J.; Munroe, J.E. (Eli Lilly and Company); Anti-viral cpds.. EP 0806408; JP 2000510468; WO 9741822 .
2 Hornback, W.J.; Mauldin, S.C.; Munroe, J.E. (Eli Lilly and Company); Anti-viral cpds.. EP 0806411; JP 2000510464; WO 9742154 .
3 Colacino, J.M.; Hornback, W.J.; Mauldin, S.C.; Munroe, J.E.; Tang, J.C.-C. (Eli Lilly and Company); Anti-viral method. WO 9741849 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 26921 (1S,4aS,10aR)-6-hydroxy-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydro-1-phenanthrenecarboxylic acid 5947-49-9 C17H22O3 详情 详情
(II) 26922 methyl (1S,4aS,10aR)-6-methoxy-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydro-1-phenanthrenecarboxylate C19H26O3 详情 详情
Extended Information