【结 构 式】 |
【分子编号】54588 【品名】(S)-(1-methyl-1H-pyrazol-5-yl)(phenyl)methanol 【CA登记号】 |
【 分 子 式 】C11H12N2O 【 分 子 量 】188.22916 【元素组成】C 70.19% H 6.43% N 14.88% O 8.5% |
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:(S)-(-)-(I)Resolution of alcohol [(±)-I] as its diastereomeric O-acetylmandelate esters and saponification of each of them in ethanol in the presence of catalytic amounts of sodium cyanide yielded the enantiomerically pure alcohols [(R)-(+)-I] and [(S)-()-I].
【1】 Hueso, J.; Frigola, J.; Farré, A.; Berrocal, J.; Gutierrez, B.; Preparation of the enantiomers of the analgesic E-3710. Bioorg Med Chem Lett 1993, 3, 2, 269. |
【2】 Farré, A.J.; Frigola, J.; Cizolirtine Citrate. Drugs Fut 2002, 27, 8, 721. |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(rac)-(I) | 54583 | (1-methyl-1H-pyrazol-5-yl)(phenyl)methanol; 5-(alpha-hydroxybenzyl)-1-methyl-1H-pyrazole | C11H12N2O | 详情 | 详情 | |
(R)-(+)-(I) | 54587 | (R)-(1-methyl-1H-pyrazol-5-yl)(phenyl)methanol | C11H12N2O | 详情 | 详情 | |
(S)-(-)-(I) | 54588 | (S)-(1-methyl-1H-pyrazol-5-yl)(phenyl)methanol | C11H12N2O | 详情 | 详情 |
Extended Information