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HRID 1350869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-(cyclopropylmethoxy)phenoxy]-N-{3-fluoro-4-[(methylsulfonyl)amino]benzyl}acetamide

https://huagongshe.com/reaction/1350869

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[4-tert-Butyl-3-(cyclopropylmethoxy)phenoxy]acetic acidHCID 21097500—
反応物N-[4-(aminomethyl)-2-fluorophenyl]methanesulfonamide hydrochlorideHCID 21097525—
溶媒TriethylamineHCID 8471—
生成物2-[4-tert-Butyl-3-(cyclopropylmethoxy)phenoxy]-N-{3-fluoro-4-[(methylsulfonyl)amino]benzyl}acetamideHCID 2109746178.6%

反応手順

[4-tert-Butyl-3-(cyclopropylmethoxy)phenoxy]acetic acid (139 mg, 0.5 mmol), 2-chloro-1,3-dimethylimidazolinium chloride (CDI) (89 mg, 0.6 mmol), triethylamine (0.2 ml) and N-[4-(aminomethyl)-2-fluorophenyl]methanesulfonamide hydrochloride (140 mg, 0.6 mmol) were treated in the same procedure described in Example 2(b). The crude residue was applied to a silica gel chromatography column and eluted with a volume mixture of hexane and ethyl acetate (3/1) to furnish 188 mg (78% yield) of the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07214824B2
出典データセットuspto-grants-2007_05
ORD IDord-57cd639bd7354aca9e2c5206037dd80c
出典メモuspto-grants-2007_05