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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 474021생성일: 2026년 10월 23일

Potassium Carbonate → 6-(3-cyclopropyl-3-fluoroazetidin-1-yl)-N-(3-methyl-1H-pyrazol-5-yl)-2-(methylsulfonyl)pyrimidin-4-amine

https://huagongshe.com/ko/reaction/474021

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Sodium BisulfiteHCID 23665763—
반응물Potassium hydroxy sulfiteHCID 23707502—
반응물HCID 178503490HCID 178503490—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물6-(3-cyclopropyl-3-fluoroazetidin-1-yl)-N-(3-methyl-1H-pyrazol-5-yl)-2-(methylsulfonyl)pyrimidin-4-amineHCID 178428245—

반응 단계

A solution of 6-(3-cyclopropyl-3-fluoroazetidin-1-yl)-N-(3-methyl-1H-pyrazol-5-yl)-2-(methylthio)pyrimidin-4-amine (130 g, 389 mmol) in MeOH (5.2 L) was cooled to 0° C. A solution of oxone (526 g, 855 mmol) in H2O (5.2 L) was slowly added to the slurry keeping the temperature below 5° C. After addition the reaction was allowed to warm to room temperature overnight. A 10% solution of NaHSO3 (325 ml) and a 10% solution of K2CO3 (2.6 L) was then added to neutralize the reaction mixture, the solution filtered and the filter cake washed with H2O (3.3 L). The solid was slurried in H2O (2.6 L), the solution filtered and the filter cake washed with H2O (3.3 L). The solid was dried under vacuum (72.3 g, 51%). 1H NMR (DMSO): 0.47 (2H, m), 0.60 (2H, m), 1.43-1.46 (1H, m), 2.20 (3H, s), 3.25 (3H, s), 3.97-4.11 (4H, m), 5.93 (1H, br s), 6.47 (1H, br s). 9.88 (1H, s), 12.01 (1H, br s). ES+367

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637511B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-26a19c91b5704bd69cf2e5dffdce3fc3
출처 메모uspto-grants-2014_01