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【结 构 式】 
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【分子编号】40118 【品名】methyl (3R,4S)-1-methyl-4-phenyl-3-piperidinecarboxylate 【CA登记号】 |
【 分 子 式 】C14H19NO2 【 分 子 量 】233.3104 【元素组成】C 72.07% H 8.21% N 6% O 13.72% |
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 methyl N-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate (I) with phenylmagnesium bromide (A) gives methyl 1-methyl-4-phenylpiperidine-3-carboxylate (II), which is reduced with LiAlH4 yielding 1-methyl-3-hydroxymethyl-4-phenylpiperidine (III), which, in turn is resolved into its optical isomers. The alcohol (III) is esterified with methanesulfonyl chloride in pyridine affording 3-(methansulfonyloxymethyl)-1-methyl-4-phenylpiperidine (IV), which is finally condensed with p-methoxyphenol (B) by means of sodium methoxide in refluxing methanol.
| 【1】 Christensen, J.A.; Squires, R.F.; 4-Phenylpiperidine compounds. DE 2404113; FR 2215233; GB 1422263; JP 49101385; JP 58174363; US 3912743 . |
| 【2】 Chatterjee, S.S.; Femoxetine. Drugs Fut 1977, 2, 5, 309. |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| (A) | 17616 | bromo(phenyl)magnesium; Phenyl Magnesium Bromide | 100-58-3 | C6H5BrMg | 详情 | 详情 |
| (B) | 32744 | 4-methoxyphenol | 150-76-5 | C7H8O2 | 详情 | 详情 |
| (I) | 38648 | methyl 1-methyl-1,2,5,6-tetrahydro-3-pyridinecarboxylate | C8H13NO2 | 详情 | 详情 | |
| (II) | 40118 | methyl (3R,4S)-1-methyl-4-phenyl-3-piperidinecarboxylate | C14H19NO2 | 详情 | 详情 | |
| (III) | 40119 | [(3R,4S)-1-methyl-4-phenylpiperidinyl]methanol | C13H19NO | 详情 | 详情 | |
| (IV) | 40120 | (3R,4S)-1-methyl-3-([[methyl(dimethylene)-lambda(6)-sulfanyl]oxy]methyl)-4-phenylpiperidine | C16H25NOS | 详情 | 详情 |
Extended Information