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HRID 417122作成日:2026年10月26日

Tributylphosphine → (4-{2-[2-(4-Chloro-phenyl)-5,6-difluoro-benzoimidazol-1-yl]-2-cyclohexyl-ethoxy}-phenoxy)-acetic acid methyl ester

https://huagongshe.com/reaction/417122

反応式

関与物質

役割名称HCID仕込み量
反応物TributylphosphineHCID 13831—
反応物Methyl 2-(4-hydroxyphenoxy)acetateHCID 602731—
反応物DiamideHCID 5353800—
反応物2-[2-(4-Chloro-phenyl)-5,6-difluoro-benzoimidazol-1-yl]-2-cyclohexyl-ethanolHCID 66619310—
生成物(4-{2-[2-(4-Chloro-phenyl)-5,6-difluoro-benzoimidazol-1-yl]-2-cyclohexyl-ethoxy}-phenoxy)-acetic acid methyl esterHCID 66619469—

反応手順

The title compound was prepared in analogy to Example 4, intermediate, from 2-[2-(4-chloro-phenyl)-5,6-difluoro-benzoimidazol-1-yl]-2-cyclohexyl-ethanol (Ex. 1, int. c), (4-hydroxy-phenoxy)-acetic acid methyl ester (commercially available), tri-n-butylphosphin and N,N′,N′-tetramethylazodicarboxamide. The compound was purified by preparative HPLC (phenomenex gemini column) eluting with a gradient of acetonitril:water (50:50 to 95:5). Colorless oil. MS (Turbo Spray): m/z=555.2 [M+H].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08088930B2
出典データセットuspto-grants-2012_01
ORD IDord-0daa727ca595437bb81804aa4b21e4f5
出典メモuspto-grants-2012_01