돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47597생성일: 2026년 10월 23일

Barium hydroxide → 4-t-Butylsulfinylaminopiperidine

https://huagongshe.com/ko/reaction/47597

반응식

참여 물질

역할이름HCID투입량
반응물Barium hydroxideHCID 6093286—
반응물4-t-Butylsulfinylamino-1-ethoxycarbonyl piperidineHCID 22747780—
용매MethanolHCID 887—
용매WaterHCID 962—
용매IsopropanolHCID 3776—
생성물4-t-ButylsulfinylaminopiperidineHCID 22747781—

반응 단계

In a mixture of 5 ml of 2-propanol and 5 ml of water, 378 mg of 4-t-butylsulfinylamino-1-ethoxycarbonyl piperidine was suspended and 1.77 g of barium hydroxide was added. The mixture was refluxed with stirring and heating for 4 hours. The mixture was diluted with methanol and the insoluble material was filtered off. The solvent was removed under reduced pressure to give 4-t-butylsulfinylaminopiperidine. Without purification, the obtained material was dissolved in 5 ml of THF, and 984 mg of N-phenoxycarbonyl-4-butyl aniline and 236 mg of diisopropyl ethylamine were added, followed by stirring at room temperature overnight. An aqueous solution of potassium hydrogen sulfate was added to the mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over magnesium sulfate anhydride. The solvent was removed under reduced pressure and the residue was purified by silica gel chromatography to give 291 mg of 4-t-butylsulfinylaminopiperidine-1-carboxlic acid(4-t-butylphenyl)amide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699891B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-6d4d1a0bbcb1440ebeca15bc76df47e0
출처 메모uspto-grants-2004_03