【结 构 式】 |
【分子编号】22992 【品名】1,2-bis(4-methoxyphenyl)-1-ethanone oxime 【CA登记号】 |
【 分 子 式 】C16H17NO3 【 分 子 量 】271.31592 【元素组成】C 70.83% H 6.32% N 5.16% O 17.69% |
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 reaction of desoxyanisoin (I) with hydroxylamine in methanol gives the corresponding oxime (I), which is cyclized with ethyl acetate (III) by means of n-butyllithium in THF yielding 3,4-di(4-methoxyphenyl)-5-methylisoxazole (IV). Finally, this compound is condensed with CO2 by means of n-butyllithium in THF.
【1】 Micetich, R.G.; Shaw, C.-C.; Rastogi, R.B. (CDC Life Sciences Inc.); 3,4-Diaryl-5-acetic acid cpds., process for prepar. EP 0026928; US 4327222 . |
【2】 Prous, J.; Castaner, J.; N-22. Drugs Fut 1988, 13, 12, 1050. |
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) | 22991 | 1,2-bis(4-methoxyphenyl)-1-ethanone | 120-44-5 | C16H16O3 | 详情 | 详情 |
(II) | 22992 | 1,2-bis(4-methoxyphenyl)-1-ethanone oxime | C16H17NO3 | 详情 | 详情 | |
(III) | 17941 | 3-Trimethylsilylpropargyl alcohol; 3-(trimethylsilyl)-2-propyn-1-ol | 5272-36-6 | C6H12OSi | 详情 | 详情 |
(IV) | 22994 | 4-[3-(4-methoxyphenyl)-5-methyl-4-isoxazolyl]phenyl methyl ether; 3,4-bis(4-methoxyphenyl)-5-methylisoxazole | C18H17NO3 | 详情 | 详情 |
Extended Information