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【结 构 式】

【分子编号】18051

【品名】5-beta-Cyano-9-alpha,11-alpha-epoxy-4,7-alpha-methano-3,4'-dioxo-17-alpha-pregnane-21,17-carbolactone

【CA登记号】

【 分 子 式 】C24H27NO5

【 分 子 量 】409.48212

【元素组成】C 70.4% H 6.65% N 3.42% O 19.54%

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:(XXVI)

Alternatively, lactone (XVIII) obtained from enol ether (XIV) as in the Scheme 3, was epoxidized to give (XXIII), which was dehydrogenated using either DDQ or chloranil to afford dienone (XXIV). Conversion to enamine (XXV), then hydrolysis to diketone (XXVI), and ring opening with NaOMe furnished eplerenone.

1 Ng, J.S.; Wang, P.T.; Baez, J.A.; Liu, C.; Anderson, D.K.; Lawson, J.P.; Erb, D.; Wieczorek, J.; Mucciariello, G.; Vanzanella, F.; Kunda, S.A.; Letendre, L.J.; Pozzo, M.J.; Sing, Y.-L.L. (Pharmacia Corp.); Process for preparation of 7 alpha-carboxyl 9,11-epoxy steroids and intermediates useful therein and a general process for the epoxidation of olifinic double bonds. WO 9721720 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(XIV) 18040 (8S,10R,13S,14S)-3-methoxy-10,13-dimethyl-1,2,7,8,10,12,13,14,15,16-decahydro-17H-cyclopenta[a]phenanthren-17-one C20H26O2 详情 详情
(XV) 18041 3-Methoxyspiro[androsta-3,5,9(11)-triene-17(S),2'-oxirane] C21H28O2 详情 详情
(XVI) 18042 21-(Ethoxycarbonyl)-3-methoxypregan-3,5,9(11)-triene-21,17-carbolactone C26H34O5 详情 详情
(XVII) 18043 3-Methoxypregna-3,5,9(11)-triene-21,17-carbolactone C23H30O3 详情 详情
(XVIII) 18044 3-Oxopregna-4,9(11)-diene-21,17-carbolactone C22H28O3 详情 详情
(XXIII) 18048 9-alpha,11-alpha-Epoxy-3-oxopregn-4-ene-21,17-carbolactone C22H28O4 详情 详情
(XXIV) 18049 9-alpha,11-alpha-Epoxy-3-oxopregna-4,6-diene-21,17-carbolactone C22H26O4 详情 详情
(XXV) 18050 4'-Amino-5-beta-cyano-9-alpha,11-alpha-epoxy-7-alpha,4-metheno-3-oxo-17-alpha-pregnane-21,17-carbolactone C24H28N2O4 详情 详情
(XXVI) 18051 5-beta-Cyano-9-alpha,11-alpha-epoxy-4,7-alpha-methano-3,4'-dioxo-17-alpha-pregnane-21,17-carbolactone C24H27NO5 详情 详情
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