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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 719510생성일: 2026년 10월 26일

Isopropyl chloroformate → {4-[1-(4-Methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yloxy]-piperidin-1-yl}-(5-morpholin-4-ylmethyl-furan-2-yl)-methanone

https://huagongshe.com/reaction/719510

반응식

참여 물질

역할이름HCID투입량
반응물Isopropyl chloroformateHCID 7917—
반응물TriethylamineHCID 8471—
반응물5-Morpholin-4-ylmethyl-furan-2-carboxylic acidHCID 580530—
반응물1-(4-methanesulfonyl-phenyl)-4-(piperidin-4-yloxy)-1H-pyrazolo[3,4-d]pyrimidineHCID 11360802—
용매Dimethyl SulfoxideHCID 679—
생성물{4-[1-(4-Methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yloxy]-piperidin-1-yl}-(5-morpholin-4-ylmethyl-furan-2-yl)-methanoneHCID 21897743—

반응 단계

5-Morpholin-4-ylmethyl-furan-2-carboxylic acid (0.12 mmol, 25 mg), and isopropylchloroformate (0.12 mmol, 17 μL) and triethylamine (0.12 mmol, 17 μL) were dissolved in DMSO (2 mL) and stirred for 30 minutes at room temperature. Then, 1-(4-methanesulfonyl-phenyl)-4-(piperidin-4-yloxy)-1H-pyrazolo[3,4-d]pyrimidine (0.12 mmol, 50 mg) and excess triethylamine were added. The mixture was heated in a microwave for 5 minutes at 120° C. The progress of the reaction was monitored by thin layer chromatography and LCMS. Purification by HPLC provided compound A116 as a white solid. LCMS (ESI), m/z 567.3 (MH+, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07132426B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-1ee15c4976f54e6f820a9e9d6abab935
출처 메모uspto-grants-2006_11