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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 260886생성일: 2026년 10월 27일

Acetic Acid → N-(4-piperidyl)-4-(N-acetyl-N-methylamino)benzenesulfonamide acetate

https://huagongshe.com/reaction/260886

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물4-(N-methylacetamido)benzene-1-sulfonyl chlorideHCID 293146—
반응물1-Benzyl-4-piperidylamineHCID 415852—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물N-(1-Benzyl-4-piperidyl)-4-(N-acetyl-N-methylamino)benzenesulfonamideHCID 15049722—
생성물N-(4-piperidyl)-4-(N-acetyl-N-methylamino)benzenesulfonamide acetateHCID 67690431100%

반응 단계

N-(1-Benzyl-4-piperidyl)-4-(N-acetyl-N-methylamino)benzenesulfonamide was prepared as a colorless oil from the 4-(N-acetyl-N-methylamino)benzenesulfonyl chloride (20.0 g, 80.8 mmol) and 4-amino-1-benzylpiperidine (18.16 ml, 88.9 mmol) in a similar manner to that described in Preparative Example 16. This oil was dissolved in ethanol (200 ml), followed by the addition of glacial acetic acid (10.0 ml). The obtained mixture was stirred in the presence of 10% palladium/carbon (water-containing one, 2.00 g) in a hydrogen atmosphere (1 atm) at 50° C. for 5 hours and filtered to remove the catalyst. The filtrate was concentrated to precipitate a crystal. The resulting mixture was washed with ethyl acetate and filtered to give the title compound as a white crystal (29.70 g, overall yield of two steps: 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05530118
출처 데이터셋uspto-grants-1996_06
ORD IDord-61daeb8a02174afeb1a6871e64eb89aa
출처 메모uspto-grants-1996_06