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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68474생성일: 2026년 10월 25일

Pyridine → N-[(3-{4-[(Acetylamino)methyl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]-5-chloro-2-thiophenecarboxamide

https://huagongshe.com/reaction/68474

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Diethyl EtherHCID 3283—
반응물Acetic AnhydrideHCID 7918—
반응물N-({3-[4-(aminomethyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)-5-chloro-2-thiophenecarboxamideHCID 21070786—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물N-[(3-{4-[(Acetylamino)methyl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]-5-chloro-2-thiophenecarboxamideHCID 21070779—

반응 단계

At 0° C., a mixture of 30 mg (0.082 mmol) of N-({3-[4-(aminomethyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)-5-chloro-2-thiophene-carboxamide (from Example 148) in 1.5 ml of absolute THF and 1.0 ml of absolute dichloromethane, and 0.02 ml of absolute pyridine is mixed with acetic anhydride (0.015 ml, 0.164 mmol). The mixture is stirred at room temperature overnight. Addition of ether and crystallization affords the product. Yield: 30 mg (87% of theory),

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822458B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-ec868296347c4d758c0de2e86b86d396
출처 메모uspto-grants-2014_09