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HRID 55270作成日:2026年10月25日

8-Bromo-2,6-dimethyloct-2-ene → 3-{6-[2-(4-methoxycarbonylphenyl)-ethinyl]-3-[(3RS)-3,7-dimethyl-6-octenyloxy]-2-pyridyl}-propionic acid methyl ester

https://huagongshe.com/reaction/55270

反応式

関与物質

役割名称HCID仕込み量
反応物8-Bromo-2,6-dimethyloct-2-eneHCID 4328245—
反応物3-{3-Hydroxy-6-[2-(4-methoxycarbonylphenyl)-ethinyl]-2-pyridyl}-propionic acid methyl esterHCID 54181731—
生成物3-{6-[2-(4-methoxycarbonylphenyl)-ethinyl]-3-[(3RS)-3,7-dimethyl-6-octenyloxy]-2-pyridyl}-propionic acid methyl esterHCID 5410374674.2%

反応手順

Under the conditions of example 1 D, 500 mg of 3-{3-hydroxy-6-[2-(4-methoxycarbonylphenyl)-ethinyl]-2-pyridyl}-propionic acid methyl ester is reacted with 354 mg of 1-bromo-(3RS)-3,7-dimethyl-6-octene, worked up, and the crude product is chromatographed on silica gel with hexane/0-10% ethyl acetate. 522 mg of 3-{6-[2-(4-methoxycarbonylphenyl)-ethinyl]-3-[(3RS)-3,7-dimethyl-6-octenyloxy]-2-pyridyl}-propionic acid methyl ester is obtained as yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624943
出典データセットuspto-grants-1997_04
ORD IDord-2a7086b666994f6d93ad082df265dd08
出典メモuspto-grants-1997_04