【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