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【结 构 式】

【分子编号】34195

【品名】6,8-dimethoxy-5-[(4-methoxybenzoyl)oxy]-2-(4-methoxyphenyl)-4-oxo-4H-chromen-7-yl 4-methoxybenzoate

【CA登记号】

【 分 子 式 】C34H28O11

【 分 子 量 】612.58972

【元素组成】C 66.66% H 4.61% O 28.73%

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:(VIII)

Nevadensin can be synthesized starting from methyl 2,6-dimethoxyphenyl acetate (I). This compound is nitrated and then hydrogenated, giving methyl 3,5-diamino-2,6-dimethoxyphenyl acetate (III). Treatment of the latter compound with stannous chloride-hydrochloric acid gives dimethoxyphloroglucinol (IV). Introduction of an acetyl group followed by interaction with p-methoxybenzoyl chloride (A) gives 4-acetyl-2,6-dimethoxyphloroglucinyl tri(p-methoxy) benzoate (VI). The latter compound, after being rearranged, is cyclized into 5,7-di(p-methoxy)benzoylnevadensin (VIII). Nevadensin can readily be obtained by the hydrolysis of the compound (VIII).

1 Feng, S.; Xu, Y.; Fan, G.; Studies on the antituberculosis principles from Lysionotus pauciflora Maxim. I. Isolation and identification of nevadensin. Acta Pharm Sin 1979, 14, 7, 447-448.
2 Su, C.; Han, G.; Zhang, Y.; Determination of nevadensin in biological specimens and its pharmacokinetic study. Chin Pharm Bull 1981, 2, 3, 182-185.
3 Ru-yun, J.; Nevadensin. Drugs Fut 1984, 9, 4, 271.
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) 22671 4-Methoxybenzoyl chloride; p-Methoxybenzoyl chloride; 4-Anisoyl chloride 100-07-2 C8H7ClO2 详情 详情
(I) 34188 2,6-dimethoxyphenyl acetate C10H12O4 详情 详情
(II) 34189 2,6-dimethoxy-3,5-dinitrophenyl acetate C10H10N2O8 详情 详情
(III) 34190 3,5-diamino-2,6-dimethoxyphenyl acetate C10H14N2O4 详情 详情
(IV) 34191 2,4-dimethoxy-1,3,5-benzenetriol C8H10O5 详情 详情
(V) 34192 1-(2,4,6-trihydroxy-3,5-dimethoxyphenyl)-1-ethanone C10H12O6 详情 详情
(VI) 34193 2-acetyl-4,6-dimethoxy-3,5-bis[(4-methoxybenzoyl)oxy]phenyl 4-methoxybenzoate C34H30O12 详情 详情
(VII) 34194 3-hydroxy-2,6-dimethoxy-5-[(4-methoxybenzoyl)oxy]-4-[3-(4-methoxyphenyl)-3-oxopropanoyl]phenyl 4-methoxybenzoate C34H30O12 详情 详情
(VIII) 34195 6,8-dimethoxy-5-[(4-methoxybenzoyl)oxy]-2-(4-methoxyphenyl)-4-oxo-4H-chromen-7-yl 4-methoxybenzoate C34H28O11 详情 详情
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