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HRID 74186作成日:2026年10月23日

Methanol → 5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoaniline

https://huagongshe.com/ja/reaction/74186

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)nitrobenzeneHCID 67498108—
触媒PalladiumHCID 23938—
溶媒TetrahydrofuranHCID 8028—
生成物5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoanilineHCID 6749880689.1%

反応手順

5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)nitrobenzene (see Working Example 20-1) (1.00 g, 0.76 mol) was dissolved in a solvent mixture of THF (50 mL) and methanol (50 mL), and Pd/C (5%, wet, 0.5 g) was added to carry out a hydrogenation reaction. After being stirred overnight at room temperature, the catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to yield the title compound (812 mg, 89.1%) as a gray solid.

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-db448fdc435e4d0a9b8ec2680e8c8fa4
出典メモuspto-grants-2014_09