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【结 构 式】

【分子编号】34935

【品名】2-(2,6-dimethylphenyl)-5-nitro-1H-isoindole-1,3(2H)-dione

【CA登记号】

【 分 子 式 】C16H12N2O4

【 分 子 量 】296.28236

【元素组成】C 64.86% H 4.08% N 9.45% O 21.6%

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:(III)

Phthalimide (III) was prepared by condensation of 4-nitrophthalic anhydride (I) with 2,6-dimethylaniline (II) in refluxing AcOH. Reduction of the nitro group of (II) by transfer hydrogenation using cyclohexene and Pd/C provided the title aminophthalimide.

1 Vamecq, J.; Lambert, D.; Poupaert, J.H.; Masereel, B.; Stables, J.P.; Anticonvulsant activity and interactions with neuronal voltage-dependent sodium channel of analogues of ameltolide. J Med Chem 1998, 41, 18, 3307.
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) 31028 5-nitro-2-benzofuran-1,3-dione 5466-84-2 C8H3NO5 详情 详情
(II) 17527 2,6-Xylidine; 2,6-Dimethylaniline; 2,6-Dimethylphenylamine 87-62-7 C8H11N 详情 详情
(III) 34935 2-(2,6-dimethylphenyl)-5-nitro-1H-isoindole-1,3(2H)-dione C16H12N2O4 详情 详情
Extended Information