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【结 构 式】

【分子编号】58593

【品名】[4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene](methyl)ammoniumolate

【CA登记号】

【 分 子 式 】C17H15Cl2NO

【 分 子 量 】320.21764

【元素组成】C 63.77% H 4.72% Cl 22.14% N 4.37% O 5%

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:(V)

The condensation of 1-naphthol (I) with an excess of o-dichlorobenzene (II) at 100 C by means of anhydrous AlCl3 gives 4-(3,4-dichlorophenyl)-1-tetralone (III), which is allowed to react with N-methylhydroxylamine (IV) and NaOAc in refluxing ethanol, yielding the nitrone (V). The reduction of (V) with H2 over RaNi in methanol affords a racemic cis/trans (9:1) mixture of methylamines, which by crystallization of its hydrochloride in ethanol provides pure (racemic)-(cis)-(VI). Finally, the target (1S)-(cis)-compound is obtained by optical resolution of (VI) with (R)-(-)-mandelic acid.

1 Vukics, K.; et al.; Improved industrial synthesis of antidepressant sertraline. Org Process Res Dev 2002, 6, 1, 82.
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) 22935 alpha-naphthol; 1-naphthol 90-15-3 C10H8O 详情 详情
(II) 58592 1,2-Dichlorobenzene; chloroben; chloroden; cloroben; Dichloricide; Dichlorobenzol; dilantin db; dilatin db; dizene; dowtherm e; o-Dichlorobenzene; o-Dichlorobenzol; termitkil 95-50-1 C6H4Cl2 详情 详情
(III) 30583 4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenone; 4-(3',4'-Dichlorophenyl)-1-tetralone 79580-19-3 C16H12Cl2O 详情 详情
(IV) 12690 (Hydroxyamino)methane; N-Methylhydroxylamine 593-77-1 CH5NO 详情 详情
(V) 58593 [4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenylidene](methyl)ammoniumolate C17H15Cl2NO 详情 详情
(VI) 58594 N-[(1S,4S)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-naphthalenyl]-N-methylamine; (1S,4S)-4-(3,4-dichlorophenyl)-N-methyl-1,2,3,4-tetrahydro-1-naphthalenamine C17H17Cl2N 详情 详情
Extended Information