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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 934생성일: 2026년 10월 23일

Water → cis-N-(3-Methoxy-4-piperidinyl)-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamide

https://huagongshe.com/ko/reaction/934

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium HydroxideHCID 14797—
반응물cis-N-(1-ethoxycarbonyl-3-methoxy-4-piperidinyl)-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamideHCID 69232225—
용매IsopropanolHCID 3776—
생성물cis-N-(3-Methoxy-4-piperidinyl)-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamideHCID 6923214516.3%

반응 단계

2.50 g of the cis-N-(1-ethoxycarbonyl-3-methoxy-4-piperidinyl)-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamide prepared in the Example 7 and 4.5 g of potassium hydroxide were dissolved in 2-propanol. The obtained solution was refluxed for 1.5 hours and cooled, followed by the addition thereto of water. The resulting mixture was extracted with 10% 2-propanol/chloroform thrice. The combined organic phases were dried over magnesium sulfate and freed from the solvent. The residue was purified by silica gel column chromatography (5 to 12% methanol/dichloromethane) to give 0.34 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723472
출처 데이터셋uspto-grants-1998_03
ORD IDord-dd08297f1095466ea20b3117b6f50645
출처 메모uspto-grants-1998_03