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【结 构 式】

【分子编号】58318

【品名】2-methyl-6-nitro-4-quinolinamine; 2-methyl-6-nitro-4-quinolinylamine

【CA登记号】

【 分 子 式 】C10H9N3O2

【 分 子 量 】203.20048

【元素组成】C 59.11% H 4.46% N 20.68% O 15.75%

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:(VII)

5-Nitroisatin (VIII) is condensed with acetone in the presence of aqueous ammonia in an autoclave at 100 C to produce the quinolinecarboxamide (IX). Subsequent Hofmann rearrangement of (IX) with sodium hypochlorite produces the 4-amino quinoline (X). The nitro group of (X) is then reduced by catalytic hydrogenation over Pd/C to give the diaminoquinoline (VII).

1 Shinkai, H.; Yamada, H.; to, T. (Japan Tobacco Inc.); Amide derivs. and nociceptin antagonists. EP 1072263; JP 1999335355; WO 9948492 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(VII) 58318 2-methyl-6-nitro-4-quinolinamine; 2-methyl-6-nitro-4-quinolinylamine C10H9N3O2 详情 详情
(VIII) 49031 4-amino-2-methyl-6-quinolinylamine; 2-methyl-4,6-quinolinediamine C10H11N3 详情 详情
(IX) 58316 5-nitro-1H-indole-2,3-dione; 5-Nitroisatin 611-09-6 C8H4N2O4 详情 详情
(X) 58317 2-methyl-6-nitro-4-quinolinecarboxamide C11H9N3O3 详情 详情
Extended Information