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【结 构 式】

【分子编号】35192

【品名】bis(2-methylphenyl)methanone

【CA登记号】

【 分 子 式 】C15H14O

【 分 子 量 】210.27556

【元素组成】C 85.68% H 6.71% O 7.61%

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:(I)

Treatment of 2,2'-dimethylbenzophenone (I) with hydroxylamine afforded oxime (II), which was reduced to the benzhydryl amine (III) with sodium metal in liquid ammonia. Condensation of (III) with bromoacetyl bromide (IV) then produced the target amide (V).

1 Chiou, W.J.; Liu, G.; Kozmina, N.S.; Opgenorth, T.J.; Winn, M.; Dixon, D.B.; Nguyen, B.; von geldern, T.W.; Marsh, K.C.; Design, synthesis, and activity of a series of pyrrolidine-3-carboxylic acid-based, highly specific, orally active ETB antagonists containing a diphenylmethylamine acetamide side chain. J Med Chem 1999, 42, 18, 3679.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
32201 Hydroxylamine 7803-49-8 H3NO 详情 详情
(I) 35192 bis(2-methylphenyl)methanone C15H14O 详情 详情
(II) 35193 bis(2-methylphenyl)methanone oxime C15H15NO 详情 详情
(III) 35194 bis(2-methylphenyl)methanamine; bis(2-methylphenyl)methylamine C15H17N 详情 详情
(IV) 14005 2-Bromoacetyl bromide; Bromoacetyl bromide 598-21-0 C2H2Br2O 详情 详情
(V) 35195 N-[bis(2-methylphenyl)methyl]-2-bromoacetamide C17H18BrNO 详情 详情
Extended Information