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【结 构 式】

【分子编号】42314

【品名】2-chloro-4-nitrophenylamine; 2-chloro-4-nitroaniline

【CA登记号】121-87-9

【 分 子 式 】C6H5ClN2O2

【 分 子 量 】172.57068

【元素组成】C 41.76% H 2.92% Cl 20.54% N 16.23% O 18.54%

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)

The condensation between 2-chloro-4-nitroaniline (II) and phthalic anhydride (I) in refluxing acetic acid produced phthalimide (III). The nitro group was then reduced to the desired aniline by transfer hydrogenation employing cyclohexene in the presence of Pd/C.

1 Herrenknecht, C.; Maurois, P.; Delcourt, P.; Stables, J.P.; Vamecq, J.; Bac, P.; Synthesis and anticonvulsant and neurotoxic properties of substituted N-phenyl derivatives of the phthalimide pharmacophore. J Med Chem 2000, 43, 7, 1311.
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) 11900 2-Benzofuran-1,3-dione;1,2-Benzenedicarboxylic Anhydride;1,2-BENZENE DICARBOXYLIC ACID ANHYDRIDE;1,2-BENZENEDICARBONIC ACID, ANHYDRIDE;1,3-DIOXOPHTHALAN;1,3-ISOBENZOFURANDIONE;o-phthalic anhydride; Phthalic anhydride 85-44-9 C8H4O3 详情 详情
(II) 42314 2-chloro-4-nitrophenylamine; 2-chloro-4-nitroaniline 121-87-9 C6H5ClN2O2 详情 详情
(III) 42315 2-(2-chloro-4-nitrophenyl)-1H-isoindole-1,3(2H)-dione C14H7ClN2O4 详情 详情
Extended Information