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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 344472생성일: 2026년 10월 26일

Water → 4-amino-5-chloro-2-methoxy-N-((1-(4-phenylsulfonylbutyl)piperidin-4-yl)methyl)benzamide hydrochloride

https://huagongshe.com/reaction/344472

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물((4-Chlorobutyl)sulfonyl)benzeneHCID 12457347—
반응물4-amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamide dihydrochlorideHCID 69966330—
용매DimethylformamideHCID 6228—
생성물4-amino-5-chloro-2-methoxy-N-((1-(4-phenylsulfonylbutyl)piperidin-4-yl)methyl)benzamide hydrochlorideHCID 7007292613.4%

반응 단계

Potassium carbonate (0.87 g) and 4-phenylsulfonylbutyl chloride (0.40 g) were added to a solution (15 ml) of 4-amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamide dihydrochloride (0.52 g) in dimethylformamide, and the mixture was stirred at 70°-80° C. for 7.5 hr. Water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with brine and dried. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography. The obtained oil was treated with hydrochloric acid-ethanol and the obtained crystals were recrystallized from ethyl acetate to give 0.10 g of 4-amino-5-chloro-2-methoxy-N-((1-(4-phenylsulfonylbutyl)piperidin-4-yl)methyl)benzamide hydrochloride.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05864039
출처 데이터셋uspto-grants-1999_01
ORD IDord-3d1d3eb1a05d48099cd4559b3de05707
출처 메모uspto-grants-1999_01