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【结 构 式】

【分子编号】63289

【品名】(E)-3-(4-{[(3,4-dimethoxyphenyl)sulfonyl]amino}phenyl)-N-(tetrahydro-2H-pyran-2-yloxy)-2-propenamide

【CA登记号】

【 分 子 式 】C22H26N2O7S

【 分 子 量 】462.52372

【元素组成】C 57.13% H 5.67% N 6.06% O 24.21% S 6.93%

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)

Acylation of 4-iodoaniline (I) with 3,4-dimethoxybenzenesulfonyl chloride (II), followed by basic methanolysis leads to sulfonamide (III). Heck coupling of aryl iodide (III) with acrylic acid (IV) in the presence of tris(dibenzylideneacetone)dipalladium and tri(o-tolyl)phosphine gives the cinnamic acid derivative (V). This is then coupled to the tetrahydropyranyl-protected hydroxylamine (VI) by means of EDC/HOBt to furnish (VII). The tetrahydropyranyl hydroxamate (VII) is finally deprotected under acidic conditions to produce the title compound.

1 Bouchain, G.; Leit, S.; Frechette, S.; et al.; Development of potential antitumor agents. Synthesis and biological evaluation of a new set of sulfonamide derivatives as histone deacetylase inhibitors. J Med Chem 2003, 46, 5, 820.
2 Lavoie, R.; Bouchain, G.; Frechette, S.; et al.; Design and synthesis of a novel class of histone deacetylase inhibitors. Bioorg Med Chem Lett 2001, 11, 21, 2847.
3 Delorme, D.; Ruel, R.; Lavoie, R.; Thibault, C.; Abou-Khalil, E. (MethylGene Inc.); Inhibitors of histone deacetylase. EP 1233958; JP 2003514904; WO 0138322 .
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) 26393 4-iodoaniline; 4-iodophenylamine 540-37-4 C6H6IN 详情 详情
(II) 47469 3,4-dimethoxybenzenesulfonyl chloride 23095-31-0 C8H9ClO4S 详情 详情
(III) 63287 N-(4-iodophenyl)-3,4-dimethoxybenzenesulfonamide C14H14INO4S 详情 详情
(IV) 19139 acrylic acid 79-10-7 C3H4O2 详情 详情
(V) 63288 (E)-3-(4-{[(3,4-dimethoxyphenyl)sulfonyl]amino}phenyl)-2-propenoic acid C17H17NO6S 详情 详情
(VI) 52106 2-(aminooxy)tetrahydro-2H-pyran; O-tetrahydro-2H-pyran-2-ylhydroxylamine C5H11NO2 详情 详情
(VII) 63289 (E)-3-(4-{[(3,4-dimethoxyphenyl)sulfonyl]amino}phenyl)-N-(tetrahydro-2H-pyran-2-yloxy)-2-propenamide C22H26N2O7S 详情 详情
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