【结 构 式】 |
【分子编号】44081 【品名】3-bromo-4-methoxybenzaldehyde 【CA登记号】34841-06-0 |
【 分 子 式 】C8H7BrO2 【 分 子 量 】215.04638 【元素组成】C 44.68% H 3.28% Br 37.16% O 14.88% |
合成路线1
该中间体在本合成路线中的序号:(I)3-Bromo-4-hydroxybenzaldehyde (I) was protected as the corresponding cyclic ketal (III) by treatment with neopentyl glycol (II) and pyridinium p-toluenesulfonate. Lithiation of (III) with n-butyllithium, followed by addition to methyl 4-methoxybenzoate (IV), furnished the triaryl carbinol (V). Deketalization of (V) with concomitant reduction of the tertiary alcohol to yield (VI) was accomplished upon heating in formic acid. Subsequent cleavage of the methoxy groups of (VI) by means of boron tribromide afforded the trihydroxy derivative (VII). Finally, dialdehyde (VII) was condensed with 1-amino-5-methyltetrazole (VIII) to generate the title bis-imine.
【1】 Pevear, D.C.; Nitz, T.J. (ViroPharma, Inc.); Cpds., compsns. and methods for treating or preventing pneumovirus infection and associated diseases. WO 9938508 . |
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) | 44081 | 3-bromo-4-methoxybenzaldehyde | 34841-06-0 | C8H7BrO2 | 详情 | 详情 |
(II) | 12641 | Neopentyl glycol; 2,2-Dimethyl-1,3-propanediol | 126-30-7 | C5H12O2 | 详情 | 详情 |
(III) | 44082 | 2-(3-bromo-4-methoxyphenyl)-5,5-dimethyl-1,3-dioxane; 2-bromo-4-(5,5-dimethyl-1,3-dioxan-2-yl)phenyl methyl ether | C13H17BrO3 | 详情 | 详情 | |
(IV) | 44083 | methyl p-anisate; methyl 4-methoxybenzoate | 121-98-2 | C9H10O3 | 详情 | 详情 |
(V) | 44084 | bis[5-(5,5-dimethyl-1,3-dioxan-2-yl)-2-methoxyphenyl](4-methoxyphenyl)methanol | C34H42O8 | 详情 | 详情 | |
(VI) | 44085 | 3-[(5-formyl-2-methoxyphenyl)(4-methoxyphenyl)methyl]-4-methoxybenzaldehyde | C24H22O5 | 详情 | 详情 | |
(VII) | 44086 | 3-[(5-formyl-2-hydroxyphenyl)(4-hydroxyphenyl)methyl]-4-hydroxybenzaldehyde | C21H16O5 | 详情 | 详情 | |
(VIII) | 44087 | 5-methyl-1H-1,2,3,4-tetraazol-1-ylamine; 5-methyl-1H-1,2,3,4-tetraazol-1-amine | C2H5N5 | 详情 | 详情 |