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【结 构 式】

【分子编号】43778

【品名】N-methyl-N-(2-nitrophenyl)-N-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalenyl)amine; N,5,5,8,8-pentamethyl-N-(2-nitrophenyl)-5,6,7,8-tetrahydro-2-naphthalenamine

【CA登记号】

【 分 子 式 】C21H26N2O2

【 分 子 量 】338.44972

【元素组成】C 74.53% H 7.74% N 8.28% O 9.45%

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)

Treatment of o-nitroaniline (I) with 6-bromo-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphtalene (II), K2CO3 and CuI in xylene yields diphenylamine derivative (III), which is then N-methylated by means of NaH and MeI in DMF to provide (IV). Reduction of the nitro group of (IV) by hydrogenation over Pd/C in ethanol or by treatment with Fe and HCl in H2O/EtOH affords the corresponding amine derivative (V), which is then condensed with terephthalic acid monomethyl ester chloride (VI) in benzene/pyridine to furnish compound (VII). Cyclization of (VII) by means of polyphosphoric acid (PPA) in CH2Cl2 gives diazepin derivative (VIII), which is finally converted in the target product by first nitration with KNO3 in H2SO4 followed by hydrolysis with NaOH in EtOH.

1 Ohta, K.; Ebisawa, M.; Umemiya, H.; et al.; Retinoid X receptor-antagonistic diazepinylbenzoic acids. Chem Pharm Bull 1999, 47, 12, 1778.
2 Shudo, K. (Nikken Chemicals Co., Ltd.); Cpds. potentiating retinoid. JP 1998059951; US 5929069; US 6121256; WO 9711061 .
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) 11608 o-Nitroaniline; 2-Nitroaniline; 2-Nitrophenylamine 88-74-4 C6H6N2O2 详情 详情
(II) 43776 6-bromo-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene C14H19Br 详情 详情
(III) 43777 5,5,8,8-tetramethyl-N-(2-nitrophenyl)-5,6,7,8-tetrahydro-2-naphthalenamine; N-(2-nitrophenyl)-N-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalenyl)amine C20H24N2O2 详情 详情
(IV) 43778 N-methyl-N-(2-nitrophenyl)-N-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalenyl)amine; N,5,5,8,8-pentamethyl-N-(2-nitrophenyl)-5,6,7,8-tetrahydro-2-naphthalenamine C21H26N2O2 详情 详情
(V) 43779 N-(2-aminophenyl)-N-methyl-N-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalenyl)amine; N(1)-methyl-N(1)-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalenyl)-1,2-benzenediamine C21H28N2 详情 详情
(VI) 25029 p-Phthalic acid monomethyl ester chloride; Terephthalic acid monomethyl ester chloride; Methyl 4-chlorocarbonylbenzoate 7377-26-6 C9H7ClO3 详情 详情
(VII) 43780 methyl 4-([2-[methyl(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalenyl)amino]anilino]carbonyl)benzoate C30H34N2O3 详情 详情
(VIII) 43781 methyl 4-(5,7,7,10,10-pentamethyl-7,8,9,10-tetrahydro-5H-naphtho[2,3-b][1,5]benzodiazepin-12-yl)benzoate C30H32N2O2 详情 详情
Extended Information