【结 构 式】 |
【分子编号】18991 【品名】2-bromo-N-isopropyl-N-phenylacetamide 【CA登记号】 |
【 分 子 式 】C11H14BrNO 【 分 子 量 】256.1423 【元素组成】C 51.58% H 5.51% Br 31.2% N 5.47% O 6.25% |
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)N-Phenyl-1,2-phenylenediamine (I) was alkylated with bromoacetanilide (II) in the presence of potassium carbonate in DMF, and the resulting alkylated phenylenediamine (III) was condensed with diacid chloride (IV) in THF to afford dioxobenzodiazepine (V). Reduction of the hydrazone function with zinc-acetic acid provided amine (VI) (1). Urea (VIII) was then prepared by treatment of amine (VI) with isocyanate (VII) in dichloromethane, and finally, ethyl ester was hydrolyzed on treatment with K2CO3 in a refluxing mixture of methanol and THF.
【1】 Hirst, G.C.; et al.; Discovery of 1,5-benzodiazepines with peripheral cholecystokinin (CCK-A) receptor agonist activity (II): Optimization of the C3 amino substituent. J Med Chem 1996, 39, 26, 5236. |
【2】 Finch, H.; Shah, P.; Carr, R.A.E. (Glaxo Wellcome plc); 1,5-Benzodiazepine derivs. having CCK and/or gastrin antagonistic activity. US 5585376; US 5646140; WO 9424149; WO 9424151 . |
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) | 18990 | N-(2-aminophenyl)-N-phenylamine; N(1)-phenyl-1,2-benzenediamine | 534-85-0 | C12H12N2 | 详情 | 详情 |
(II) | 18991 | 2-bromo-N-isopropyl-N-phenylacetamide | C11H14BrNO | 详情 | 详情 | |
(III) | 18992 | 2-(2-anilinoanilino)-N-isopropyl-N-phenylacetamide | C23H25N3O | 详情 | 详情 | |
(IV) | 17971 | 2-(2-phenylhydrazono)malonoyl dichloride | C9H6Cl2N2O2 | 详情 | 详情 | |
(V) | 18994 | 2-[2,4-dioxo-5-phenyl-3-[(Z)-2-phenylhydrazono]-4,5-dihydro-1H-1,5-benzodiazepin-1(2H)-yl]-N-isopropyl-N-phenylacetamide | C32H29N5O3 | 详情 | 详情 | |
(VI) | 18995 | 2-(3-amino-2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-1-yl)-N-isopropyl-N-phenylacetamide | C26H26N4O3 | 详情 | 详情 | |
(VII) | 18996 | ethyl 3-isocyanatobenzoate | 67531-68-4 | C10H9NO3 | 详情 | 详情 |
(VIII) | 18997 | ethyl 3-[[([1-[2-(isopropylanilino)-2-oxoethyl]-2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-3-yl]amino)carbonyl]amino]benzoate | C36H35N5O6 | 详情 | 详情 |
Extended Information