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【结 构 式】

【分子编号】52002

【品名】 

【CA登记号】

【 分 子 式 】C23H22O4

【 分 子 量 】362.42528

【元素组成】C 76.22% H 6.12% O 17.66%

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:(IV)

The peroxidation of 1,4-diphenyl-1-cyclopentadiene (I) with O2, white light and activated by tetraphenylporphyrin in dichloromethane gives the peroxide (II), which is condensed with cyclohexane-1,4-dione (III) by means of trimethylsilyl trifluoromethanesulfonate in dichloromethane, yielding the adduct (IV). The reductocondensation of (IV) with N-(7-chloroquinolin-4-yl)ethylenediamine (V) by means of NaBH(OAc)3 in dichloromethane affords the tricyclic trioxane (VI), which is finally treated with citric acid in acetone to provide the target citrate. The intermediate N-(7-chloroquinolin-4-yl)ethylenediamine (V) has been obtained by reaction of 4,7-dichloroquinoline (VIII) with ethylenediamine by means of NaOH at 85 C.

1 Dechy-Cabaret, O.; et al.; Preparation of antimalarial activities of "trioxaquines", new modular molecules with a trioxane skeleton linked to a 4-aminoquinoline. ChemBioChem 2000, 1, 4, 281.
2 Robert, A.; Dechy Cabaret, O.; Meunier, B.; Benoit Vical, F. (CNRS (Centre National de la Recherche Scientifique)); Dual molecules containing a peroxide deriv., synthesis and therapeutic applications thereof. FR 2807433; WO 0177105 .
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) 51999 1-(4-phenyl-1,3-cyclopentadien-1-yl)benzene C17H14 详情 详情
(II) 52000 1,4-diphenyl-2,3-dioxabicyclo[2.2.1]hept-5-ene C17H14O2 详情 详情
(III) 52001 1,4-Cyclohexanedione; Tetrahydro-p-benzoquinone 637-88-7 C6H8O2 详情 详情
(IV) 52002   C23H22O4 详情 详情
(V) 52003 N(1)-(6-chloro-1-naphthyl)-1,2-ethanediamine; N-(2-aminoethyl)-N-(6-chloro-1-naphthyl)amine C12H13ClN2 详情 详情
(VI) 52004   C35H35ClN2O3 详情 详情
(VII) 13856 2-Hydroxy-1,2,3-propanetricarboxylic acid; Citric acid 77-92-9 C6H8O7 详情 详情
(VIII) 52005 1,6-dichloronaphthalene C10H6Cl2 详情 详情
(IX) 14754 ethylenediamine;1,2-Diaminoethane;ethane-1,2-diamine;1,2-Ethanediamine 107-15-3 C2H8N2 详情 详情
Extended Information