돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74186생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)nitrobenzeneHCID 67498108—
촉매PalladiumHCID 23938—
용매TetrahydrofuranHCID 8028—
생성물5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoanilineHCID 6749880689.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829035B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-db448fdc435e4d0a9b8ec2680e8c8fa4
출처 메모uspto-grants-2014_09