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【结 构 式】

【分子编号】27040

【品名】6-(trifluoromethyl)-5-[[6-(trifluoromethyl)-2,3-dihydro-1H-indol-5-yl]disulfanyl]indoline

【CA登记号】

【 分 子 式 】C18H14F6N2S2

【 分 子 量 】436.4450592

【元素组成】C 49.54% H 3.23% F 26.12% N 6.42% S 14.69%

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:(III)

The reaction of 6-(trifluoromethyl)indoline (I) with potassium thiocyanate and Br2 in methanol gives 5-thiocyanato-6-(trifluoromethyl)indoline (II), which is treated with ammonia in hot dioxane/water yielding the disulfide (III). The acylation of (III) with acetic anhydride and triethylamine in dichloromethane affords the corresponding diacetyl derivative (IV), which is treated with triphenylphosphine and conc. HCl in refluxing dioxane to give 5-sulfanyl-6-(trifluoromethyl)-indoline (V). The methylation of (V) with methyl iodide and K2CO3 in hot DMF yields the methylsulfanyl compound (VI), which is deacetylated with NaOH in refluxing ethanol/water affording 5-(methylmsulfanyl)-6--(trifluoromethyl)-indoline (VII). Finally, this compound is condensed with 3-pyridyl isothiocyanate (VIII) in toluene. The indoline (VII) can also be obtained directly from indoline (I) by reaction of (I) with potassium thiocyanate and Br2 in methanol, followed by a treatment with methyl iodide and KOH. The 3-pyridyl isocyanate can be obtained by decomposition of pyridine-3-carboxylic acid azide (IX) in refluxing toluene.

1 Bromidge, S.M.; et al.; Novel and selective 5-HT2C/2B receptor antagonists as potential anxiolytic agents: Synthesis, quantitative structure-activity relationships, and molecular modeling of substituted 1-(3-pyridylcarbamoyl)indolines. J Med Chem 1998, 41, 10, 1598.
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) 27038 6-(trifluoromethyl)indoline C9H8F3N 详情 详情
(II) 27039 6-(trifluoromethyl)-5-indolinesulfenyl cyanide C10H7F3N2S 详情 详情
(III) 27040 6-(trifluoromethyl)-5-[[6-(trifluoromethyl)-2,3-dihydro-1H-indol-5-yl]disulfanyl]indoline C18H14F6N2S2 详情 详情
(IV) 27041 1-[5-[[1-acetyl-6-(trifluoromethyl)-2,3-dihydro-1H-indol-5-yl]disulfanyl]-6-(trifluoromethyl)-2,3-dihydro-1H-indol-1-yl]-1-ethanone C22H18F6N2O2S2 详情 详情
(V) 27042 1-[5-sulfanyl-6-(trifluoromethyl)-2,3-dihydro-1H-indol-1-yl]-1-ethanone C11H10F3NOS 详情 详情
(VI) 27043 1-[5-(methylsulfanyl)-6-(trifluoromethyl)-2,3-dihydro-1H-indol-1-yl]-1-ethanone C12H12F3NOS 详情 详情
(VII) 27044 5-(methylsulfanyl)-6-(trifluoromethyl)indoline C10H10F3NS 详情 详情
(VIII) 27045 3-isocyanatopyridine 15268-31-2 C6H4N2O 详情 详情
(IX) 13619 Nicotinoyl azide C6H4N4O 详情 详情
Extended Information