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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxylamine HCl | HCID 21645 | — |
| Reactant | 3-(2,5-dimethylpyrrol-1-yl)-1-(3-fluorophenyl)-5-iodo-1H-pyrazole | HCID 86680355 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | 1-(3-Fluorophenyl)-5-iodo-1H-pyrazol-3-ylamine | HCID 86680354 | 89.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846746B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-4958583d39724c58a3f05e282281cb19 |
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| Source note | uspto-grants-2014_09 |
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