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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1427010생성일: 2026년 10월 26일

Potassium Hydroxide → 1-(1-((tert-butoxy)carbonyl)piperidin-4-yl)-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/1427010

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물Tert-butyl 4-(4-(ethoxycarbonyl)-1H-pyrazol-1-YL)piperidine-1-carboxylateHCID 45926154—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물1-(1-((tert-butoxy)carbonyl)piperidin-4-yl)-1H-pyrazole-4-carboxylic acidHCID 5348589782%

반응 단계

tert-Butyl 4-(4-(ethoxycarbonyl)-1H-pyrazol-1-yl)piperidine-1-carboxylate described in Production Example 13-2 (2.11 g, 6.53 mmol) was dissolved in methanol (60 mL), then potassium hydroxide (1.46 g, 26.1 mmol) dissolved in water (16 mL) was added, and then the mixture was stirred for 27 hours. The reaction mixture was concentrated under vacuum and diethyl ether was added for partition. Ethyl acetate was added to the aqueous layer for dilution, then a 5% aqueous potassium hydrogensulfate solution was added for acidification, and the mixture was extracted with ethyl acetate twice. The combined organic layer was dried over anhydrous magnesium sulfate and filtered. The solvent was evaporated to obtain the title compound (1.58 g, 82%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08933099B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-883a07d1c3fe4d91b9caad0dafa139ef
출처 메모uspto-grants-2015_01