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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83544Generated: October 29, 2026

Triethylamine → HCID 86680375, compound

https://huagongshe.com/reaction/83544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydroxylamine HClHCID 21645—
ReactantHCID 86680376HCID 86680376—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 86680375HCID 8668037564%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a suspension of 3-(2,5-dimethylpyrrol-1-yl)-1-(4-fluorophenyl)-5-iodo-1H-pyrazole (625 mg) in ethanol/water (2/1, 12.5 ml) were sequentially added hydroxylammonium chloride (2.28 g) and triethylamine (0.46 ml) at room temperature, and the mixture was stirred at 95° C. for 15 hours. This reaction mixture was cooled to room temperature, concentrated under reduced pressure. To the resulting residue was added a 8M aqueous solution of sodium hydroxide, and then the mixture was extracted with ethyl acetate. This organic layer was sequentially washed with water and a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=1/1) to give the titled compound (318 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846746B2
Source datasetuspto-grants-2014_09
ORD IDord-e79e609dee64437a932e0d8e38630821
Source noteuspto-grants-2014_09