【结 构 式】 |
【分子编号】39674 【品名】4-methoxy-2-nitrophenyl phenyl ether; 4-methoxy-2-nitro-1-phenoxybenzene 【CA登记号】 |
【 分 子 式 】C13H11NO4 【 分 子 量 】245.23468 【元素组成】C 63.67% H 4.52% N 5.71% O 26.1% |
合成路线1
该中间体在本合成路线中的序号:(II)A preparative-scale synthetic route for T-614 has been reported: The reaction of 4-chloro-3-nitroanisole (I) with potassium phenolate in hot DMF gives 4-phenoxy-3-nitroanisole (II), which is reduced to the corresponding 3-amino compound (III) by treatment with Fe and HCl. The reaction of (III) with mesyl chloride in pyridine affords the sulfonamide (IV), which is acylated with 2-aminoacetonitrile (V) and AlCl3 in nitrobenzene/HCl giving the 2-aminoacetophenone (VI). Formylation of (VI) at the NH2 with acetic formic anhydride yields the formamide (VII), which is demethylated with AlCl3 and NaI in acetonitrile affording the phenol (VIII). Finally, this compound is cyclized with dimethylformamide dimethylacetal in DMF.
【1】 Yoshida, C.; Tanaka, K.; Nagaki, H.; Takeno, R.; Inaba, T.; Takano, S.; Synthesis and antiinflammatory activities of 7-methanesulfonylamino-6-phenoxychromones. Antiarthritic effect of the 3-formylamino compound (T-614) in chronic inflammatory disease models. Chem Pharm Bull 2000, 48, 1, 131. |
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) | 24772 | 1-chloro-4-methoxy-2-nitrobenzene | 10298-80-3 | C7H6ClNO3 | 详情 | 详情 |
(II) | 39674 | 4-methoxy-2-nitrophenyl phenyl ether; 4-methoxy-2-nitro-1-phenoxybenzene | C13H11NO4 | 详情 | 详情 | |
(III) | 39675 | 5-methoxy-2-phenoxyphenylamine; 5-methoxy-2-phenoxyaniline | C13H13NO2 | 详情 | 详情 | |
(IV) | 39676 | N-(5-methoxy-2-phenoxyphenyl)methanesulfonamide | C14H15NO4S | 详情 | 详情 | |
(V) | 39680 | 2-aminoacetonitrile | C2H4N2 | 详情 | 详情 | |
(VI) | 39677 | N-[4-(2-aminoacetyl)-5-methoxy-2-phenoxyphenyl]methanesulfonamide | C16H18N2O5S | 详情 | 详情 | |
(VII) | 39678 | N-[4-[2-(formylamino)acetyl]-5-methoxy-2-phenoxyphenyl]methanesulfonamide | C17H18N2O6S | 详情 | 详情 | |
(VIII) | 39679 | N-[4-[2-(formylamino)acetyl]-5-hydroxy-2-phenoxyphenyl]methanesulfonamide | C16H16N2O6S | 详情 | 详情 | |
(IX) | 11984 | N-(Dimethoxymethyl)-N,N-dimethylamine;dimethylformamide dimethylacetal;1,1-dimethoxy-N,N-dimethylmethanamine; Dimethoxy-N,N-dimethylmethanamine; N,N-Dimethylformamide dimethyl acetal | 4637-24-5 | C5H13NO2 | 详情 | 详情 |