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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74158생성일: 2026년 10월 23일

4-((Tetrahydropyran-4-yl)amino)-3-nitrobenzoic acid → 3-Amino-4-((tetrahydropyran-4-yl)amino)benzoic acid

https://huagongshe.com/ko/reaction/74158

반응식

참여 물질

역할이름HCID투입량
반응물4-((Tetrahydropyran-4-yl)amino)-3-nitrobenzoic acidHCID 43610332—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물3-Amino-4-((tetrahydropyran-4-yl)amino)benzoic acidHCID 54888048100.2%

반응 단계

4-((Tetrahydropyran-4-yl)amino)-3-nitrobenzoic acid (see Working Example 4-1) (202 g, 0.76 mol) was dissolved in a solvent mixture of THF (2.2 L) and methanol (1.5 L), Pd/C (5%, wet, 20 g) was added, and hydrogenation was carried out under 5 atm. Hydrogen absorption stopped at 3 h, and after the system was purged with argon the catalyst was removed by filtration, and the filtrate was concentrated at reduced pressure to yield the title compound (180 g, quant.) as a dark gray solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829035B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-b340ee561d764d2ea478af19f7930b3d
출처 메모uspto-grants-2014_09