【结 构 式】 |
【分子编号】39960 【品名】triamcinolone cyclopentanonide 【CA登记号】55646-99-6 |
【 分 子 式 】C26H33FO6 【 分 子 量 】460.5428232 【元素组成】C 67.81% H 7.22% F 4.13% O 20.84% |
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:(III)9alpha,fluoro-11beta16alpha,17,21-tetrahydroxypregna-1,4-diene-3,20-dione (I) is ketalized by reaction with cyclopentanone (II) by means of perchloric acid yielding the ketal (III), which is then acetylated by reaction with acetic anhydride in pyridine.
【1】 Hillier, K.; Castaner, J.; Amcinodine. Drugs Fut 1978, 3, 5, 337. |
【2】 Sieger, G.M.; Krieger, C. (American Cyanamid Co.); Administration of 16alpha,17alpha-cyclopentylidenedioxy-9alpha-fluoro-11beta,21-dihydroxy-1,4-pregnadiene-3,20-dione-21-acetate. DE 2437847; FR 2240738; GB 1442925; US 4158055 . |
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) | 39959 | (8S,9R,10S,11S,13S,14S,16R,17S)-9-fluoro-17-glycoloyl-11,16,17-trihydroxy-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-3-one | 124-94-7 | C21H27FO6 | 详情 | 详情 |
(II) | 15113 | cyclopentanone | 120-92-3 | C5H8O | 详情 | 详情 |
(III) | 39960 | triamcinolone cyclopentanonide | 55646-99-6 | C26H33FO6 | 详情 | 详情 |
Extended Information