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【结 构 式】

【分子编号】53125

【品名】4-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)benzenesulfonyl chloride

【CA登记号】n/a

【 分 子 式 】C14H8ClNO4S

【 分 子 量 】321.74056

【元素组成】C 52.26% H 2.51% Cl 11.02% N 4.35% O 19.89% S 9.97%

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:(IV)

The condensation of phthalic anhydride (I) with aniline (II) in refluxing HOAc produced N-phenyl phthalimide (III). Aromatic sulfonation of (III) with chlorosulfonic acid in the presence of PCl5 afforded the sulfonyl chloride (IV). This was finally condensed with thiomorpholine (V) to furnish the target sulfonamide.

1 Legora, A.M.; et al.; Anti-inflammatory effects of thalidomide-derived compounds on LPS-induced inflammation in mouse lung. Inflamm Res 2001, 50, Suppl. 3, Abst 083.
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) 12294 Aniline; Phenylamine 62-53-3 C6H7N 详情 详情
(III) 53124 N-Phenylphthalimide 520-03-6 C14H9NO2 详情 详情
(IV) 53125 4-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)benzenesulfonyl chloride n/a C14H8ClNO4S 详情 详情
(V) 36317 thiomorpholine 123-90-0 C4H9NS 详情 详情
Extended Information