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【结 构 式】

【分子编号】53836

【品名】1-methoxy-4-methyl-1,4-cyclohexadiene; methyl 4-methyl-1,4-cyclohexadien-1-yl ether

【CA登记号】n/a

【 分 子 式 】C8H12O

【 分 子 量 】124.18268

【元素组成】C 77.38% H 9.74% O 12.88%

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:(II)

The partial reduction of 4-methylanisole (I) with sodium in liquid ammonia/THF/ethanol gives the enol ether (II), which is condensed with 2-chloro-6-fluoroaniline (III) by means of TiCl4 in chlorobenzene/THF to yield the imine (IV), which, without isolation, is aromatized with I2 in AcOH/THF to provide N-(2-chloro-6-fluorophenyl)-N-(4-methylphenyl)amine (V). The acylation of (V) with 2-chloroacetyl chloride (VI) at 90 C affords the 2-chloroacetamide (VII), which is cyclized by means of AlCl3 by heating at 160?C to afford 1-(2-chloro-6-fluorophenyl)-5-methylindolin-2-one (VIII). Finally, this compound is hydrolyzed with NaOH in refluxing ethanol/water and acidified with 1N HCl. Alternatively, the intermediate N-(2-chloro-6-fluorophenyl)-N-(4-methylphenyl)amine (V) can also be obtained by condensation of 2-chloro-N-(4-methylphenyl)acetamide (IX) with 2-chloro-6-fluorophenol (X) by means of K2CO3 in isopropanol to yield 2-(2-chloro-6-fluorophenoxy)-N-(4-methylphenyl)acetamide (XI), which is treated with MeONa in methanol to obtain the target secondary amine (V).

1 Bayes, M.; Silvestre, J.S.; Sorbera, L.A.; Castaner, J.; Lumiracoxib. Drugs Fut 2002, 27, 8, 740.
2 Xu, D.; Allmendinger, T.; Acemoglu, M.; Calienni, J.V.; Cercus, J.; Loiseleur, O.; Sedelmeier, G. (Novartis AG; Novartis-Erfindungen VmbH); Process for phenylacetic acid derivs.. WO 0123346 .
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) 53835 1-Methoxy-4-methylbenzene; 4-Methylanisole; Methyl P-Tolyl Ether; p-Cresyl methyl ether; 4-Methoxytoluene 104-93-8 C8H10O 详情 详情
(II) 53836 1-methoxy-4-methyl-1,4-cyclohexadiene; methyl 4-methyl-1,4-cyclohexadien-1-yl ether n/a C8H12O 详情 详情
(III) 53837 2-Chloro-6-fluoroaniline 363-51-9 C6H5ClFN 详情 详情
(IV) 53838 N-(2-chloro-6-fluorophenyl)-N-(4-methyl-2-cyclohexen-1-ylidene)amine; 2-chloro-6-fluoro-N-(4-methyl-2-cyclohexen-1-ylidene)aniline n/a C13H13ClFN 详情 详情
(V) 53839 2-chloro-6-fluoro-N-(4-methylphenyl)aniline; N-(2-chloro-6-fluorophenyl)-N-(4-methylphenyl)amine n/a C13H11ClFN 详情 详情
(VI) 11296 2-Chloroacetyl chloride; Chloroacetic chloride 79-04-9 C2H2Cl2O 详情 详情
(VII) 53840 2-chloro-N-(2-chloro-6-fluorophenyl)-N-(4-methylphenyl)acetamide n/a C15H12Cl2FNO 详情 详情
(VIII) 53841 1-(2-chloro-6-fluorophenyl)-5-methyl-1,3-dihydro-2H-indol-2-one n/a C15H11ClFNO 详情 详情
(IX) 31229 2-chloro-N-(4-methylphenyl)acetamide C9H10ClNO 详情 详情
(X) 53842 2-chloro-6-fluorophenol 2040-90-6 C6H4ClFO 详情 详情
(XI) 53843 2-(2-chloro-6-fluorophenoxy)-N-(4-methylphenyl)acetamide n/a C15H13ClFNO2 详情 详情
Extended Information