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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661288Generated: October 26, 2026

1,1'-Carbonyldiimidazole → [3-(3-Ethoxy-1,2,4-oxadiazol-5-yl)-5-(4-ethylphenyl)piperidin-1-yl](3-hydroxyazetidin-1-yl)methanone

https://huagongshe.com/reaction/661288

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant5-(4-Ethylphenyl)-1-[(3-hydroxyazetidin-1-yl)carbonyl]piperidine-3-carboxylic acidHCID 58002369—
Reactantethyl N-hydroxyimidocarbamateHCID 76223295—
SolventDimethylformamideHCID 6228—
Solvent1,4-DioxaneHCID 31275—
Product[3-(3-Ethoxy-1,2,4-oxadiazol-5-yl)-5-(4-ethylphenyl)piperidin-1-yl](3-hydroxyazetidin-1-yl)methanoneHCID 58116469—

Reaction Steps

To a solution of 80.0 mg (0.241 mmol) of the carboxylic acid from Example 14A in 0.97 ml of DMF and 1.93 ml of 1,4-dioxane were added, at 60° C., 99.8 mg (0.615 mmol) of 1,1′-carbonyldiimidazole, and the mixture was stirred for 3 h. Subsequently, the mixture was admixed with 50.1 mg (0.481 mmol) of ethyl N′-hydroxyimidocarbamate [G. Zinner, G. Nebel, Arch. Pharm. 1970, 303, 385-390] and then stirred at RT for 2 h and then at 120° C. for 2.5 h. The reaction solution was concentrated under reduced pressure and purified directly by means of preparative HPLC. Yield: 33.1 mg (33% of theory)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084469B2
Source datasetuspto-grants-2011_12
ORD IDord-83d071207a4d4db8a0b1634e005a7d80
Source noteuspto-grants-2011_12