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【结 构 式】

【分子编号】30713

【品名】6-(2-oxiranyl)-2-phenyl-4H-[1,3]dioxino[5,4-b]pyridin-5-ium-5-olate

【CA登记号】

【 分 子 式 】C15H13NO4

【 分 子 量 】271.27256

【元素组成】C 66.41% H 4.83% N 5.16% O 23.59%

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:(V)

A new method for the synthesis of pirbuterol hydrochloride has been described: By reaction of 2-phenyl-4H-1,3-dioxino[5,4-b]pyridine-6-carbaldehyde (I) with methyltriphenylphosphonium bromide (II) and NaOH in toluene to give 2-phenyl-6-vinyl-4H-1,3-dioxino[5,4-b]pyridine (III), which is treated with m-chloroperbenzoic acid (IV) in methylene chloride to give 6-(1,2-epoxyethyl)-2-phenyl-4H-1,3-dioxino[5,4-b]pyridine N-oxide (V). Compound (V) can also be obtained from 6-(1,2-epoxyethyl)-2-phenyl-4H-1,3-dioxino[5,4-b]pyridine (VI) by reaction with m-chloroperbenzoic acid (IV) as before. The reaction of (V) with tert-butylamine (VII) in methanol affords 6-(1-hydroxy-2-tert-butylaminoethyl)-2-phenyl-4H-1,3-dioxino[5,4-b]pyridine N-oxide (VIII), which is first treated with H2 over Pd/C in methanol and then with HCl in ethyl acetate to give pirbuterol hydrochloride.

1 Masset, S.S.; Cue, B.W. (Pfizer Inc.); Process and intermediates for preparing pirbuteol and analogs. EP 0058069; EP 0058070; EP 0058071; EP 0058072; JP 57150665 .
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) 30711 2-phenyl-4H-[1,3]dioxino[5,4-b]pyridine-6-carbaldehyde C14H11NO3 详情 详情
(II) 30484 Methyl(triphenyl)phosphonium bromide 1779-49-3 C19H18BrP 详情 详情
(III) 30712 2-phenyl-6-vinyl-4H-[1,3]dioxino[5,4-b]pyridine C15H13NO2 详情 详情
(V) 30713 6-(2-oxiranyl)-2-phenyl-4H-[1,3]dioxino[5,4-b]pyridin-5-ium-5-olate C15H13NO4 详情 详情
(VI) 30714 6-(2-oxiranyl)-2-phenyl-4H-[1,3]dioxino[5,4-b]pyridine C15H13NO3 详情 详情
(VII) 17895 2-Amino-2-methylpropane; tert-butylamine; 2-methyl-2-propanamine 75-64-9 C4H11N 详情 详情
(VIII) 30715 6-[2-(tert-butylamino)-1-hydroxyethyl]-2-phenyl-4H-[1,3]dioxino[5,4-b]pyridin-5-ium-5-olate C19H24N2O4 详情 详情
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