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【结 构 式】

【分子编号】40191

【品名】bromo(3-chlorophenyl)magnesium

【CA登记号】

【 分 子 式 】C6H4BrClMg

【 分 子 量 】215.75946

【元素组成】C 33.4% H 1.87% Br 37.03% Cl 16.43% Mg 11.26%

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:(IX)

The reduction of 2'-oxospiro-(1,3-dioxolane-2,3'-indoline)-1'-propionitrile (V) with H2 over Raney-Ni in NH3 saturated ethanol gives 2'-oxospiro-(1,3-dioxolane-2,3'-indoline)-1'-propanamine (VI), which, without isolation, is cyclized in refluxing xylene yielding 3',4'-dihydrospiro[1,3-dioxolane-2,10'(2H,10H)pyrimido-[1,2-a]indole] (VII). The hydrolysis of (VII) with aqueous HCl at 85 C affords 3,4-dihydropyrimido[1,2-a]indole-10(2H)-one (VIII), which is finally treated with m-chlorophenylmagnesium bromide (IX) in refluxing ethyl ether.

1 White, A.C.; Black, R.M. (John Wyeth & Brother Ltd.); Fused ring indole derivatives. DE 2200584; ES 398678; ES 409296; FR 2121699; GB 1366133 .
2 Weetman, D.F.; Castaner, J.; Ciclazindol. Drugs Fut 1977, 2, 8, 508.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(V) 40187 N-cyanoethyl-3-spiro(2-ethylenedioxy)oxindole C13H12N2O3 详情 详情
(VI) 40188   C13H18N2O2 详情 详情
(VII) 40189   C13H14N2O2 详情 详情
(VIII) 40190 3,4-dihydropyrimido[1,2-a]indol-10(2H)-one C11H10N2O 详情 详情
(IX) 40191 bromo(3-chlorophenyl)magnesium C6H4BrClMg 详情 详情
Extended Information