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【结 构 式】

【分子编号】12693

【品名】6-(4-Chlorophenyl)-N-hydroxy-N-methyl-4,6-dioxohexanamide

【CA登记号】

【 分 子 式 】C13H14ClNO4

【 分 子 量 】283.7112

【元素组成】C 55.04% H 4.97% Cl 12.5% N 4.94% O 22.56%

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)

A new method for the synthesis of tepoxalin has been reported: The cyclization of 6-(4-chlorophenyl)-4,6-dioxohexanoic acid (I) with refluxing acetic anhydride gives 5-[2-(4-chlorophenyl)-2-oxoethylidene]tetrahydrofuran-2-one (II), which is treated with methylhydroxylamine to afford the corresponding N-hydroxy-N-methylamide (III). Finally, this compound is cyclized with 4-methoxyphenylhydroazine (IV) by means of Na2CO3 in refluxing ethanol.

1 Murray, W.V.; Hadden, S.K.; A facile synthesis of tepoxalin, 5-(4-chlorophenyl)-N-hydroxy-1-(4-methoxyphenyl)-N-methyl-1H-pyrazole-3-propanamide. J Org Chem 1992, 57, 24, 6662.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
12690 (Hydroxyamino)methane; N-Methylhydroxylamine 593-77-1 CH5NO 详情 详情
(I) 12687 6-(4-Chlorophenyl)-4,6-dioxohexanoic acid C12H11ClO4 详情 详情
(II) 12692 5-[(Z)-2-(4-Chlorophenyl)-2-oxoethylidene]dihydro-2-furanone C12H9ClO3 详情 详情
(III) 12693 6-(4-Chlorophenyl)-N-hydroxy-N-methyl-4,6-dioxohexanamide C13H14ClNO4 详情 详情
(IV) 12688 4-Hydrazinophenyl methyl ether; 1-(4-Methoxyphenyl)hydrazine 3471-32-7 C7H10N2O 详情 详情
Extended Information