【结 构 式】 |
【分子编号】35193 【品名】bis(2-methylphenyl)methanone oxime 【CA登记号】 |
【 分 子 式 】C15H15NO 【 分 子 量 】225.29024 【元素组成】C 79.97% H 6.71% N 6.22% O 7.1% |
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:(II)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