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HRID 13283作成日:2026年10月25日

Ethyl chloroformate → ethyl 2-(5-(4-fluorophenoxy)-2-(pyridin-2-yl)-1H-benzo[d]imidazol-6-yl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/13283

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl chloroformateHCID 10928—
反応物5-(4-fluoro-phenoxy)-2-pyridin-2-yl-6-pyrrolidin-2-yl-1H-benzimidazoleHCID 23145575—
触媒ZincHCID 23994—
溶媒BenzeneHCID 241—
生成物ethyl 2-(5-(4-fluorophenoxy)-2-(pyridin-2-yl)-1H-benzo[d]imidazol-6-yl)pyrrolidine-1-carboxylateHCID 23145223—

反応手順

5.2 mg of zinc powder and 0.006 ml of ethyl chloroformate were added in order to a benzene (1 ml) solution of 20 mg of 5-(4-fluoro-phenoxy)-2-pyridin-2-yl-6-pyrrolidin-2-yl-1H-benzimidazole obtained in Example 168, and the reaction liquid was stirred overnight at room temperature. The reaction solvent was evaporated away under reduced pressure, and the resulting residue was purified through partitioning thin-layer chromatography (Kieselgel™ 60F254, Art 5744 (by Merck), chloroform/methanol=10/1) to obtain the entitled compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728025B2
出典データセットuspto-grants-2010_06
ORD IDord-3e5e65171b8849119f3790876982c93e
出典メモuspto-grants-2010_06