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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734289Generated: October 25, 2026

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

https://huagongshe.com/reaction/734289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiethyl EtherHCID 3283—
ReactantAcetic AnhydrideHCID 7918—
ReactantN-({3-[4-(aminomethyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)-5-chloro-2-thiophenecarboxamideHCID 21070786—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductN-[(3-{4-[(Acetylamino)methyl]phenyl}-2-oxo-1,3-oxazolidin-5-yl)methyl]-5-chloro-2-thiophenecarboxamideHCID 21070779—

Reaction Steps

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),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592339B2
Source datasetuspto-grants-2009_09
ORD IDord-13d7722a6d274033bba2911e2051a80a
Source noteuspto-grants-2009_09