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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202967Generated: November 1, 2026

Pyridine → HCID 89691230, compound

https://huagongshe.com/reaction/2202967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 89690958HCID 89690958—
SolventTetrahydrofuranHCID 8028—
ProductHCID 89691230HCID 8969123018.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

Trifluoroacetic anhydride (0.181 ml) was added to a solution of (1RS,2SR)-2-(6-(4-((4-chlorobenzyl)oxy)-2-oxopyridin-1(2H)-yl)-1-methyl-1H-benzimidazol-2-yl)cyclopropanecarboxamide (195 mg) and pyridine (0.105 ml) in THF (5 ml) at 0° C. The mixture was stirred at 0° C. for 2 h. The mixture was quenched with saturated NaHCO3 solution at 0° C. and extracted with EtOAc. The organic layer was separated, washed with water and brine, dried over MgSO4 and concentrated in vacuo. The residue was purified by silica gel column chromatography (MeOH/EtOAc). The residue was recrystallized from EtOH/hexane to give the title compound (35 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365540B2
Source datasetuspto-grants-2016_06
ORD IDord-53c16f9d7df1476e93cf7b1850699c9a
Source noteuspto-grants-2016_06