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HRID 731575생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/731575

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 번호US07585860B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-02484cd7ef3b4135b700a773be416c88
출처 메모uspto-grants-2009_09