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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1958380생성일: 2026년 10월 26일

Fusaric Acid → (5-Butyl-pyridin-2-yl)-{4-[1-(4-methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yloxy]-piperidin-1-yl}-methanone

https://huagongshe.com/reaction/1958380

반응식

참여 물질

역할이름HCID투입량
반응물Fusaric AcidHCID 3442—
반응물Isopropyl chloroformateHCID 7917—
반응물TriethylamineHCID 8471—
반응물1-(4-Methanesulfonyl-phenyl)-4-(piperidin-4-yloxy)-1H-pyrazolo[3,4-d]pyrimidine hydrochlorideHCID 21897774—
용매DimethylformamideHCID 6228—
생성물(5-Butyl-pyridin-2-yl)-{4-[1-(4-methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yloxy]-piperidin-1-yl}-methanoneHCID 2189778514.3%

반응 단계

5-Butyl-pyridine-2-carboxylic acid (92 mg, 0.51 mmol) and isopropyl chloroformate (70 μL, 0.51 mmol) were dissolved in DMF and stirred at room temperature for 40 min. 1-(4-Methanesulfonyl-phenyl)-4-(piperidin-4-yloxy)-1H-pyrazolo[3,4-d]pyrimidine hydrochloride (70 mg, 0.17 mmol) and triethylamine (72 μL, 0.51 mmol) were added next and continued to stir for 24 hours. Progress of the reaction was monitored by TLC and LCMS. Removal of organic solvents in vacuo and purification by HPLC afforded Compound A125 as a white solid (13 mg, 13%). Exact mass calculated for C22H30N6O4S 534.63, found 535.20 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08410119B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-49a3fc5e5da04a82b14236ff5ee9f892
출처 메모uspto-grants-2013_04