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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416852Generated: November 1, 2026

Triethylamine → HCID 22632966, compound

https://huagongshe.com/reaction/2416852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantO-tert-butylhydroxylamine hydrochlorideHCID 2777906—
ReactantHCID 22633013HCID 22633013—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22632966HCID 2263296623.4%

Reaction Steps

A solution of 2-cyclopropylamino-3,5-difluoro-4-pyrrolidin-1-yl-benzoic acid (Example T-3, 1.65 g, 5.85 mmol) in THF (20 mL) was reacted with carbonyldiimidazole (1.2 g, 7.31 mmol) and stirred overnight at ambient temperature. The mixture was reacted with triethylamine (1.22 mL, 8.77 mmol) and O-t-butyl hydroxylamine hydrochloride (1.10 g, 8.77 mmol) and allowed to stir for 4 hours. The mixture was quenched with H2O and extracted with ethyl acetate. The organic layers were combined, dried with sodium sulfate, and concentrated. The resulting residue was dissolved in THF (15 mL), reacted with carbonyldiimidazole (2.44 g, 15.0 mmol), and heated to 100° C. in a sealed tube for 5 days. The mixture was cooled, diluted with H2O, and extracted with ethyl acetate. The organic layer was washed with H2O, dried with sodium sulfate, and concentrated. The residue was purified by column chromatography (silica gel, 1:1 hexanes/ethyl acetate) to provide 0.52 g of the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825199B2
Source datasetuspto-grants-2004_11
ORD IDord-acbb5c43706b4134b31eb506c974c688
Source noteuspto-grants-2004_11