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HRID 734289생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/734289

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 번호US07592339B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-13d7722a6d274033bba2911e2051a80a
출처 메모uspto-grants-2009_09