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【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