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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080098Generated: October 28, 2026

Pyridine → HCID 23130497, compound

https://huagongshe.com/reaction/2080098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant5-Benzyloxy-thiophene-2-carbaldehydeHCID 23130695—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 23130497HCID 2313049717.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

The resulting 5-benzyloxy-thiophene-2-carbaldehyde (171 mg) was dissolved in N,N-dimethylformamide (4 mL), pyridine (82 μl, 1.02 mmol) and hydroxylamine hydrochloride (65 mg, 0.94 mmol) were added thereto, followed by stirring for 30 minutes at 60° C., then, cooled on an ice bath. 1,1′-Carbonyldiimidazole (635 mg, 3.92 mmol) was added, the solution was warmed again to 60° C. and stirred for 35 minutes, triethylamine (272 μl, 1.96 mmol) was added, and the solution was further stirred for 30 minutes. The reaction mixture was cooled to room temperature, water was added, and the solution was extracted with ethyl acetate. The organic layer was sequentially washed with an aqueous solution of oxalic acid, an aqueous solution of saturated sodium bicarbonate and brine, dried over anhydrous sodium sulfate, and then, concentrated in vacuo. The resulting residue was purified by silica gel chromatography (hexane-ethyl acetate), and the title compound (30 mg, 0.14 mmol, 14%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-fedfc1abb2b4489f9919741eb1e5ed6a
Source noteuspto-grants-2011_04