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【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%

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)

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
Extended Information