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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1666733생성일: 2026년 10월 26일

p-Toluenesulfonic acid → 4-Tert-Butyl-N-(5-Hydroxy-4-Methyl-2-(2-Oxo-3-Phenylindolin-3-Yl)Phenyl)Benzenesulfonamide

https://huagongshe.com/reaction/1666733

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물3-Hydroxy-3-phenyl-1,3-dihydroindol-2-oneHCID 15806—
반응물4-tert-butyl-N-(3-hydroxy-4-methylphenyl)benzenesulfonamideHCID 838083—
용매1,1-DichloroethaneHCID 6365—
생성물4-Tert-Butyl-N-(5-Hydroxy-4-Methyl-2-(2-Oxo-3-Phenylindolin-3-Yl)Phenyl)BenzenesulfonamideHCID 1041454089.4%

반응 단계

As another non-limiting example, 4-tert-butyl-N-[5-hydroxy-4-methyl-2-(2-oxo-3-phenyl-2,3-dihydro-1H-indol-3-yl)-phenyl]-benzenesulfonamide (compound 1430) was synthesized by adding dropwise 4-tert-butyl-benzenesulfonyl chloride (8 g, 34 mmol) in 5 mL dichloromethane to a stirring solution of 5-Amino-2-methyl-phenol (4 g, 32 mmol) in 20 mL pyridine and letting the mixture spin overnight at room temperature. The resulting mixture was concentrated in vacuo and the product was purified by column chromatography to yield 8 g (78%) of 4-tert-butyl-N-(3-hydroxy-4-methyl-phenyl)-benzenesulfonamide. A mixture of 3-hydroxy-3-phenyl-1,3-dihydro-indol-2-one (3.9 g, 17 mmol), 4-tert-butyl-N-(3-hydroxy-4-methyl-phenyl)-benzenesulfonamide (7 g, 22 mmol) and p-toluenesulfonic acid (6.5 g, 32 mmol) in dichloroethane was refluxed for 12 hours. The resulting mixture was cooled to room temperature to yield a colorless solid. The solid was filtered and purified using column chromatography to yield 8 g (88%) of the desired product (compound 1430).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08044089B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-2b376ab1fdac4251a1061d6b942182c5
출처 메모uspto-grants-2011_10