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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7620생성일: 2026년 10월 23일

Methanol → (2-methylsulfonyl-6-(morpholin-4-yl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine

https://huagongshe.com/ko/reaction/7620

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Potassium hydroxy sulfiteHCID 23707502—
반응물[2-methylsulfanyl-6-(morpholin-4-yl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amineHCID 178419055—
용매WaterHCID 962—
생성물(2-methylsulfonyl-6-(morpholin-4-yl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amineHCID 178419103—

반응 단계

To a suspension of the above-prepared [2-methylsulfanyl-6-(morpholin-4-yl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine (500 mg, 1.63 mmol) in MeOH (10 mL) is added a solution of oxone (3.0 g) in water (10 mL). The reaction mixture is stirred at room temperature for 15 hours and most of the solvent is evaporated. The residue is partitioned between DCM and aqueous saturated NaHCO3. The organic layer is washed with brine, dried, filtered and evaporated. The residue is triturated in MeOH and the resulting white solid is collected by filtration to give [2-methylsulfonyl-6-(morpholin-4-yl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087603B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-bc09a3a13dce4855b85b4efddef0a94f
출처 메모uspto-grants-2006_08