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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 395259생성일: 2026년 10월 26일

Methyl morpholine oxide → Pnu-288034

https://huagongshe.com/reaction/395259

반응식

참여 물질

역할이름HCID투입량
반응물Methyl morpholine oxideHCID 82029—
반응물N-({(5S)-3-[3,5-difluoro-4-(4-thiomorpholinyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamideHCID 10109766—
반응물Propan-2-one--water (1/1)HCID 18366337—
촉매Osmium TetroxideHCID 30318—
생성물Pnu-288034HCID 993100383%

반응 단계

N-({(5S)-3-[3,5-difluoro-4-(4-thiomorpholinyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamide (13.36 g, 35.97 mmol) is dissolved in a solution of 25% water/acetone and then treated sequentially with 4-Methylmorpholine N-oxide (3 eq, 12.64 g, 107.91 mmol) and a catalytic amount of osmium tetroxide (2.8 mL). The reaction is stirred overnight at room temperature under nitrogen. In the morning, another 2 mL of osmium tetroxide is added. Another 2 eq of 4-Methylmorpholine N-oxide and 2.5 mL of osmium tetroxide are added a few hours later. The reaction is stirred overnight again under nitrogen. The following morning, the reaction is complete. The reaction mixture is quenched with a solution of sodium hydrosulfite and then extracted with methylene chloride three times. The organic layer is washed with sodium hydrosulfite and brine, dried with sodium sulfate, filtered, and concentrated. The crude product is then chomatographed on silica gel, eluting with methylene chloride and then 2% and 5% methanol/methylene chloride solutions. Appropriate fractions are combined and concentrated to yield 11.99 g (83%) of the title compound as a white solid, mp: 187-189.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06605609B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-eb7c889ddbf840c1bf7be46c3dbc5558
출처 메모uspto-grants-2003_08