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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 512970생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/512970

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물Sodium hydrideHCID 24758—
반응물ethyl 1H-pyrazole-4-carboxylateHCID 142179—
반응물1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물1-(1-((tert-butoxy)carbonyl)piperidin-4-yl)-1H-pyrazole-4-carboxylic acidHCID 5348589740.6%

반응 조건

온도100 °C

반응 단계

A mixture of ethyl 1H-pyrazole-4-carboxylate (700 mg, 5 mmol) and NaH 60% (6 mmol) was stirred under nitrogen at 0° C. for 1 hour in dry DMF (15 mL). tert-Butyl 4-[(methylsulfonyl)oxy]piperidine-1-carboxylate (1.53 gr, 5.5 mmol) dissolved in 4 mL of dry DMF was added and the resulting solution was heated at 100° C. overnight. Reaction mixture was quenched with water and extracted (×3) with ethyl acetate. Collected organic phases were dried over Na2SO4, filtered and evaporated to dryness. Residue was dissolved in MeOH (20 mL) and water (5 mL) and KOH (1.12 gr, 20 mmol) was added. The resulting solution was stirred at room temperature 24 hours, then solvents removed under reduced pressure. The residue was taken-up with AcOEt and KHSO4 5% solution. Aqueous phase was extracted with EtOAc several times. Collected organic phases were dried with Na2SO4, filtered and evaporated to dryness affording 600 mg of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09102662B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-c74e290262b749e096a219d203999feb
출처 메모uspto-grants-2015_08