【结 构 式】 |
【分子编号】36345 【品名】2-(4-[[6-(cyclohexyloxy)-2-naphthyl]oxy]phenyl)acetyl chloride 【CA登记号】 |
【 分 子 式 】C24H23ClO3 【 分 子 量 】394.89752 【元素组成】C 73% H 5.87% Cl 8.98% O 12.15% |
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)4-[6-(Cyclohexyloxy)-2-naphthyloxy]phenylacetic acid (I) was converted to acid chloride (II) by treatment with oxalyl chloride and catalytic DMF. Subsequent coupling of (II) with methyl anthranilate (III) produced the corresponding amide (IV). The methyl ester group of (IV) was finally hydrolyzed with LiOH in THF-MeOH.
【1】 Takenouchi, K.; Takahashi, K.; Hasegawa, M.; Takeuchi, T.; Komoriya, K. (Teijin Ltd.); Naphthalene deriv.. EP 0763523; US 5945450; WO 9532943 . |
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) | 36344 | 2-(4-[[6-(cyclohexyloxy)-2-naphthyl]oxy]phenyl)acetic acid | C24H24O4 | 详情 | 详情 | |
(II) | 36345 | 2-(4-[[6-(cyclohexyloxy)-2-naphthyl]oxy]phenyl)acetyl chloride | C24H23ClO3 | 详情 | 详情 | |
(III) | 11161 | methyl 2-aminobenzoate; Methyl anthranilate | 134-20-3 | C8H9NO2 | 详情 | 详情 |
(IV) | 36346 | methyl 2-[[2-(4-[[6-(cyclohexyloxy)-2-naphthyl]oxy]phenyl)acetyl]amino]benzoate | C32H31NO5 | 详情 | 详情 |
Extended Information