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HRID 74257作成日:2026年10月26日

2-(4-Neopentylamino-3-nitrophenyl)benzoxazole → 2-(2-Neopentylaminoanilin-5-yl)benzoxazole

https://huagongshe.com/reaction/74257

反応式

関与物質

役割名称HCID仕込み量
反応物2-(4-Neopentylamino-3-nitrophenyl)benzoxazoleHCID 67499014—
反応物HCID 178418361HCID 178418361—
触媒HCID 178418390HCID 178418390—
溶媒TetrahydrofuranHCID 8028—
生成物2-(2-Neopentylaminoanilin-5-yl)benzoxazoleHCID 6749786689.2%

反応手順

To a tetrahydrofuran solution (5 mL) of 2-(4-neopentylamino-3-nitrophenyl)benzoxazole (see Working Example 81-1) (242 mg, 0.744 mmol) was added 10% palladium-carbon (40 mg), a hydrogen atmosphere was substituted in the flask, and this was stirred at room temperature for 15 hours. After the reaction was complete, this was filtered through Celite and the filtrate was concentrated. The residue obtained was purified by silica gel column chromatography to yield the title compound (196 mg, 89% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829035B2
出典データセットuspto-grants-2014_09
ORD IDord-11f03d1e0fb8423a8aaa20d19de03e28
出典メモuspto-grants-2014_09