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【结 构 式】

【分子编号】60932

【品名】2-chloro-N-phenylacetamide

【CA登记号】

【 分 子 式 】C8H8ClNO

【 分 子 量 】169.61036

【元素组成】C 56.65% H 4.75% Cl 20.9% N 8.26% O 9.43%

与该中间体有关的原料药合成路线共 2 条

合成路线1

该中间体在本合成路线中的序号:(I)

By condensation of chloroacetinilide (I) and dimethylaminoacetanilide (II) in refluxing xylene

1 (Aktiebolaget Astra Apoketarnes Keiniska Frabriker); BE 614154; GB 995256 .
2 Castaner, J.; Hopkins, S.J.; Carcainium chloride. Drugs Fut 1977, 2, 1, 12.
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) 60932 2-chloro-N-phenylacetamide C8H8ClNO 详情 详情
(II) 60933 2-(dimethylamino)-N-phenylacetamide C10H14N2O 详情 详情

合成路线2

该中间体在本合成路线中的序号:(III)

Acylation of aniline (I) with chloroacetyl chloride (II) in cold CH2Cl2 provides 2-chloro-N-phenylacetamide (III). Then, condensation of (III) with 4-aminoquinaldine (IV) in the presence of NaH in an inert atmosphere furnishes the title compound

1 Sahu, N.P.; et al.; Synthesis of a novel quinoline derivative, 2-(2-methylquinolin-4-ylamino)-N-phenylacetamide- A potential antileishmanial agent. Bioorg. Med. Chem. 2002, 10, 6, 1687.
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) 12294 Aniline; Phenylamine 62-53-3 C6H7N 详情 详情
(II) 11296 2-Chloroacetyl chloride; Chloroacetic chloride 79-04-9 C2H2Cl2O 详情 详情
(III) 60932 2-chloro-N-phenylacetamide C8H8ClNO 详情 详情
(IV) 61469 4-Aminoquinaldine; 4-Amino-2-methylquinoline; 4-Amino-2-Methylquinoline; 4-Aminoquinaldine; 4-Amino-2-methylchinolin 6628-04-2 C10H10N2 详情 详情
Extended Information