【结 构 式】 |
【分子编号】42782 【品名】2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-6-chromanol 【CA登记号】59-02-9 |
【 分 子 式 】C29H50O2 【 分 子 量 】430.7148 【元素组成】C 80.87% H 11.7% O 7.43% |
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)By condensation of D-glucopyranuronic acid methyl ester (I) with 2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-3,4-dihydro-2H-1-benzopyran-6-ol (III) by means of Tms-OTf.
【1】 Taraporewala, I.B.; Kauffman, J.M.; Synthesis and structure activity relationships of anti-inflammatory 9,10-dihydro-9-oxo-2-acridine-alkanoic acids and 4-(2-carboxyphenyl)aminobenzenealkanoic acids. J Pharm Sci 1990, 79, 2, 173. |
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) | 42279 | 2,2,2-trichloroacetonitrile; Trichloromethylcyanide | 545-06-2 | C2Cl3N | 详情 | 详情 |
(II) | 42780 | (trimethylsilyl)[(2S,3R,4S,5R,6S)-3,4,5-tris(acetoxy)-6-(methoxycarbonyl)tetrahydro-2H-pyran-2-yl]oxonium trifluoromethanesulfonate | C17H27F3O13SSi | 详情 | 详情 | |
(III) | 42782 | 2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-6-chromanol | 59-02-9 | C29H50O2 | 详情 | 详情 |
Extended Information