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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83499Generated: October 25, 2026

Triethylamine → 1-(3-Fluorophenyl)-5-iodo-1H-pyrazol-3-ylamine

https://huagongshe.com/reaction/83499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydroxylamine HClHCID 21645—
Reactant3-(2,5-dimethylpyrrol-1-yl)-1-(3-fluorophenyl)-5-iodo-1H-pyrazoleHCID 86680355—
SolventEthyl acetate hexaneHCID 21226206—
Product1-(3-Fluorophenyl)-5-iodo-1H-pyrazol-3-ylamineHCID 8668035489.4%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a solution of 3-(2,5-dimethylpyrrol-1-yl)-1-(3-fluorophenyl)-5-iodo-1H-pyrazole (4.5 g) in ethanol/water (2/1, 81 ml) were sequentially added hydroxylammonium chloride (16.3 g) and triethylamine (3.3 ml), and the mixture was stirred at 95° C. for 17 hours. This reaction mixture was cooled to room temperature and concentrated under reduced pressure. To the resulting residue was added an 8M aqueous solution of sodium hydroxide, and 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 concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=2/1) to give the titled compound (3.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846746B2
Source datasetuspto-grants-2014_09
ORD IDord-4958583d39724c58a3f05e282281cb19
Source noteuspto-grants-2014_09