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HRID 230588作成日:2026年10月26日

1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chloride → 2-(4-Tert-butyl-3,5-difluorophenoxy)-N-((1R)-1-{3-fluoro-4-[(methylsulfonyl)amino]phenyl}ethyl)acetamide

https://huagongshe.com/reaction/230588

反応式

関与物質

役割名称HCID仕込み量
反応物1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chlorideHCID 10986715—
反応物N-{4-[(1R)-1-aminoethyl]-2-fluorophenyl}methanesulfonamide hydrochlorideHCID 66841089—
反応物(4-tert-Butyl-3,5-difluorophenoxy)acetic acidHCID 68804332—
溶媒TriethylamineHCID 8471—
生成物2-(4-Tert-butyl-3,5-difluorophenoxy)-N-((1R)-1-{3-fluoro-4-[(methylsulfonyl)amino]phenyl}ethyl)acetamideHCID 5776292337%

反応手順

(4-tert-Butyl-3,5-difluorophenoxy)acetic acid (166 mg, 0.68 mmol), 2-chloro-1,3-dimethylimidazolinium chloride (CDI) (110 mg, 0.68 mmol), triethylamine (0.5 ml) and N-{4-[(1R)-1-aminoethyl]-2-fluorophenyl}methanesulfonamide hydrochloride (183 mg, 0.68 mmol) were mixed by the same procedure as described in Example 1(e) to give 115 mg (37%) of the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07566739B2
出典データセットuspto-grants-2009_07
ORD IDord-958f5bc5e2c7406e8a469acd75604569
出典メモuspto-grants-2009_07