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【结 构 式】

【分子编号】30110

【品名】2,5-Dioxospiro[imidazolidine-4,4'-[2]oxabicyclo[3,1,0]hexane]-6'-carboxylic acid ethyl ester

【CA登记号】

【 分 子 式 】C10H12N2O5

【 分 子 量 】240.21576

【元素组成】C 50% H 5.04% N 11.66% O 33.3%

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:(X)

Cycloaddition of ethyl diazoacetate to furan (XXII) in the presence of dirhodium tetraacetate gave bicyclic compound (XXIII). Hydroboration of the olefin group of (XXIII) with tert-hexylborane, followed by oxidative treatment with hydrogen peroxide provided alcohol (XXIV), which was oxidized to ketone (IX) under Swern conditions. The title compound was then obtained as above by formation of hydantoin (X), ester hydrolysis, resolution as before, and hydrolysis of the hydantoin.

1 Massey, S.M.; Monn, J.A.; Valli, M.J. (Eli Lilly and Company); Excitatory amino acid derivs.. US 5688826 .
2 Massey, S.M.; Monn, J.A.; Valli, M.J. (Eli Lilly and Company); Excitatory amino acid derivs.. EP 0774461; JP 2000500748; WO 9718199 .
3 Levine, L.R. (Eli Lilly and Company); Treatment for premenstrual dysphoric disorder. WO 9832436 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
30108 (1,1,2-trimethylpropyl)borane C6H15B 详情 详情
(IX) 30095 ethyl 4-oxo-2-oxabicyclo[3.1.0]hexane-6-carboxylate C8H10O4 详情 详情
(X) 30110 2,5-Dioxospiro[imidazolidine-4,4'-[2]oxabicyclo[3,1,0]hexane]-6'-carboxylic acid ethyl ester C10H12N2O5 详情 详情
(XXII) 22732 benzhydryl (7R)-7-amino-3-[[methyl(dimethylene)-lambda(6)-sulfanyl]oxy]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate C23H24N2O4S2 详情 详情
(XXIII) 30107 ethyl 2-oxabicyclo[3.1.0]hex-3-ene-6-carboxylate C8H10O3 详情 详情
(XXIV) 30109 ethyl (4R)-4-hydroxy-2-oxabicyclo[3.1.0]hexane-6-carboxylate C8H12O4 详情 详情
Extended Information