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【结 构 式】 
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【分子编号】24070 【品名】2-methoxyphenylhydrosulfide 【CA登记号】7217-59-6 |
【 分 子 式 】C7H8OS 【 分 子 量 】140.20592 【元素组成】C 59.97% H 5.75% O 11.41% S 22.87% |
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：(I)The cyclization of 3-(2-methoxyphenylthio)propionic acid (II) with PPA yields 8 methoxythiochroman-4-one (III). Thiochromanone (III) is then reduced to 8-hydroxythiochromane (IV) by the Wolff-Kishner reduction method. Demethylation is almost complete during this reduction. The 8-hydroxythiochromane (IV), treated with epichlorohydrin, yields the corresponding epoxide (V), which when treated with excess tert-butylamine yields tertatolol base.
| 【1】 Leclerc, G.; Tertatolol hydrochloride. Drugs Fut 1986, 11, 2, 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) | 24070 | 2-methoxyphenylhydrosulfide | 7217-59-6 | C7H8OS | 详情 | 详情 |
| (II) | 24071 | 3-[(2-methoxyphenyl)sulfanyl]propionic acid | C10H12O3S | 详情 | 详情 | |
| (III) | 24072 | 8-methoxy-2,3-dihydro-4H-thiochromen-4-one | C10H10O2S | 详情 | 详情 | |
| (IV) | 24073 | 8-thiochromanol | C9H10OS | 详情 | 详情 | |
| (V) | 24074 | 2-[(3,4-dihydro-2H-thiochromen-8-yloxy)methyl]oxirane | C12H14O2S | 详情 | 详情 |
Extended Information