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【结 构 式】

【分子编号】68211

【品名】4-oxo-1,4-dihydroquinoline-3-carboxylic acid

【CA登记号】13721-01-2

【 分 子 式 】C10H7NO3

【 分 子 量 】189.17052

【元素组成】C 63.49% H 3.73% N 7.4% O 25.37%

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:(VII)

O-Protection of 2,4-di-tert-butylphenol (I) with methyl chloroformate (II) in the presence of Et3N and DMAP in CH2Cl2 gives 2,4-ditert-butylphenyl methyl carbonate (III), which by nitration with HNO3 and H2SO4 provides a mixture of the 5- and 6-nitrophenyl carbonates (IVa) and (IVb), respectively. Hydrolysis of the mixture of carbonates (IVa) and (IVb) by means of KOH in MeOH followed by chromatographic separation of the resulting mixture of nitrophenols affords 2,4-di-tert-butyl-5-nitrophenol (V), which is reduced by transfer hydrogenation with HCOONH4 in the presence of Pd/C in refluxing EtOH to the amine (VI). Finally, amine (VI) is condensed with 4-oxo-1,4-dihydroquinoline-3-carboxylic acid (VII) by means of HBTU and Et3N in DMF or CH2Cl2 .
4-Oxo-1,4-dihydroquinoline-3-carboxylic acid (VII) is prepared by coupling of diethyl 2-(ethoxymethylene)malonate (VIII) with aniline (IX) by heating at 140-150 °C to afford diethyl 2-(anilinomethylene) malonate (X), which by cyclization by means of PPA and POCl3 at 70 °C yields ethyl 4-oxo-1,4-dihydroquinoline-3-carboxylate (XI). Finally, ethyl ester derivative (XI) is saponified with NaOH at reflux, followed by acidification with HCl .

1 Hadida Ruah, S.S., Hazlewood, A.R., Grootenhuis, P.D.J., Van Goor, F.F., Singh, A.K., Zhou, J., McCartney, J. (Vertex Pharmaceuticals, Inc.).Modulators of ATP-binding cassette transporters. CN 10193301, EP 1773816, JP 2008504291, US 2006074075, US 7495013, US 8101767, WO 2006002421.
2 Hurter, P. (Vertex Pharmaceuticals, Inc.). Solid forms of N-[2,4-bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinoline-3-carboxamide. EP 1993360, JP 200952278, US 011064811, WO 2007079139.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IVa) 68207 2,4-di-tert-butyl-5-nitrophenyl methyl carbonate 873055-55-1 C16H23NO5 详情 详情
(IVb) 68208 2,4-di-tert-butyl-6-nitrophenyl methyl carbonate   详情 详情
(I) 68205 2,4-di-tert-butylphenol;2,4-Bis(1,1-dimethylethyl)-phenol 96-76-4 C14H22O 详情 详情
(II) 16993 methyl chlorocarbonate;Carbonochloridic acid methyl ester;[(chlorocarbonyl)oxy]methane;methyl chloroformate 79-22-1 C2H3ClO2 详情 详情
(III) 68206 2,4-ditert-butylphenyl methyl carbonate   C16H24O3 详情 详情
(V) 68209 2,4-di-tert-butyl-5-nitrophenol   C14H21NO3 详情 详情
(VI) 68210 5-amino-2,4-di-tert-butylphenol   C14H23NO 详情 详情
(VII) 68211 4-oxo-1,4-dihydroquinoline-3-carboxylic acid 13721-01-2 C10H7NO3 详情 详情
(VIII) 14088 Diethyl ethoxymethylenemalonate; Diethyl 2-(ethoxymethylene)malonate 87-13-8 C10H16O5 详情 详情
(IX) 12294 Aniline; Phenylamine 62-53-3 C6H7N 详情 详情
(X) 35953 diethyl 2-(anilinomethylene)malonate C14H17NO4 详情 详情
(XI) 68212 ethyl 4-oxo-1,4-dihydroquinoline-3-carboxylate   C12H11NO3 详情 详情
Extended Information