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HRID 1372644作成日:2026年10月25日

5-Fluoro-o-tolyl Isothiocyanate → Methyl (2-(5-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate

https://huagongshe.com/reaction/1372644

反応式

関与物質

役割名称HCID仕込み量
反応物5-Fluoro-o-tolyl IsothiocyanateHCID 519443—
反応物HCID 17859032HCID 17859032—
溶媒MethanolHCID 887—
生成物Methyl (2-(5-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetateHCID 4460752156%

反応手順

In methanol (30 ml) was dissolved methyl (4-amino-2-fluoro-3-hydroxyphenyl)acetate (1.0 g, 5.02 mmol). To the resulting solution was added 5-fluoro-2-methylphenyl isothiocyanate (1.0 g, 5.98 mmol). After the resulting mixture was stirred at room temperature for 5 days, mercuric oxide (yellow) (1.14 g, 4.36 mmol) was added thereto. The mixture was stirred at 70° C. for 6 hours. After cooling to room temperature, the reaction mixture was filtered through Celite and washed with methanol. The filtrate was distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from chloroform/ethyl acetate (30/1, v/v) eluate fractions, methyl (2-(5-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate (810 mg, 56% (2 steps)) was obtained as a pink solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07157487B2
出典データセットuspto-grants-2007_01
ORD IDord-672c550ec85c4431afa5341f70e99fc0
出典メモuspto-grants-2007_01