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【结 构 式】

【分子编号】62400

【品名】2-chloro-N-methyl-2-phenylacetamide

【CA登记号】

【 分 子 式 】C9H10ClNO

【 分 子 量 】183.63724

【元素组成】C 58.87% H 5.49% Cl 19.31% N 7.63% O 8.71%

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:(IX)

Treatment of alpha-chlorophenylacetyl chloride (VIII) with methylamine provided the corresponding chloro amide (IX), which was subsequently condensed with 2-aminobenzyl alcohol (X) to afford amino alcohol (XI). Cyclization of (XI) in the presence of AlCl3 led to the dibenzoazepine (XII). This was converted to the tetracyclic compound (XIV) by reaction with dibromoethane (XIII) in the presence of Na2CO3. Reduction of the amide carbonyl group of (XIV) by means of LiAlH4 furnished the title compound. In a related strategy, amide (XII) was initially reduced to diamine (VI) by using LiAlH4. Subsequent condensation of (VI) with dibromoethane (XIII) led to the target tetracyclic derivative

1 Haider, A.; Bollinger, H.; Fischer, A. (Sochinaz SA); Process for the preparation of a tetracyclic compound and application of this process for the preparation of 1,2,3,4,10,14b-hexahydro-2-methyldibenzo[c,f]pyrazino[1,2-a]azepin. FR 2647114 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(VI) 62397 6,11-dihydro-5H-dibenzo[b,e]azepin-6-yl-N-methylmethanamine; N-(6,11-dihydro-5H-dibenzo[b,e]azepin-6-ylmethyl)-N-methylamine C16H18N2 详情 详情
(VIII) 62399 2-chloro-2-phenylacetyl chloride C8H6Cl2O 详情 详情
(IX) 62400 2-chloro-N-methyl-2-phenylacetamide C9H10ClNO 详情 详情
(X) 18619 (2-aminophenyl)methanol; 2-Amino-benzenemethanol;2-Hydroxymethyl aniline;2-aminobenzyl alcohol;o-Aminobenzyl 2-aminobenzylalcohol;alcohol; 2-aminobenzenemethanol; 2-aminobenzyl alcohol 5344-90-1 C7H9NO 详情 详情
(XI) 62401 2-[2-(hydroxymethyl)anilino]-N-methyl-2-phenylacetamide C16H18N2O2 详情 详情
(XII) 62402 N-methyl-6,11-dihydro-5H-dibenzo[b,e]azepine-6-carboxamide C16H16N2O 详情 详情
(XIII) 10252 1,2-Dibromoethane; Ethylene dibromide 106-93-4 C2H4Br2 详情 详情
(XIV) 62403 2-methyl-3,4,10,14b-tetrahydrodibenzo[c,f]pyrazino[1,2-a]azepin-1(2H)-one C18H18N2O 详情 详情
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