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【结 构 式】

【药物名称】Wy-41770

【化学名称】(5H-Dibenzo[a,d]cyclohepten-5-ylidene)acetic acid
      5H-Dibenzo[a,d]cycloheptene-DELTA(5,alpha)acetic acid
      Dibenzo[a,d]cycloheptatrienylideneacetic acid

【CA登记号】4517-99-1

【 分 子 式 】C17H12O2

【 分 子 量 】248.28399

【开发单位】Wyeth Pharmaceuticals (Originator)

【药理作用】Antiarthritic Drugs, IMMUNOMODULATING AGENTS, Immunomodulators, TREATMENT OF MUSCULOSKELETAL & CONNECTIVE TISSUE DISEASES

合成路线1

The Wittig condensation of triethyl phosphonoacetate (II) with 5H-dibenzo[a,d]cyclohepten-5-one (I) by means of NaH in DMSO gives the ethyl (III), which is finally hydrolyzed with KOH in refluxing ethanol.

1 Bergmann, E.D.; Solomonovici, A.; Fulvenes and thermochromic ethylenes. 57. Wittig-Homer reaction with fulvene ketones and related ketones. Synthesis 1970, 2, 4, 183-189.
2 Wolf, M. (American Home Products Corp.); Method for treating inflammation. EP 0035903; GB 2071098; JP 82500244; US 4267192 .
3 Serradell, M.N.; Castaner, J.; Arrigoni-Martelli, E.; WY-41770. Drugs Fut 1985, 10, 4, 309.
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) 29151 5H-dibenzo[a,d]cyclohepten-5-one; Dibenzosuberenone 2222-33-5 C15H10O 详情 详情
(II) 10019 Ethyl 2-(diethoxyphosphoryl)acetate; Triethyl phosphonoacetate 867-13-0 C8H17O5P 详情 详情
(III) 29152 ethyl 2-(5H-dibenzo[a,d]cyclohepten-5-ylidene)acetate C19H16O2 详情 详情
Extended Information