HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748753Generated: October 30, 2026
Potassium Carbonate → N'-hydroxy-1-methyl-5-nitro-1H-pyrazole-3-carboximidamide
https://huagongshe.com/reaction/1748753
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 1-methyl-5-nitro-1H-pyrazole-3-carbonitrile | HCID 50896717 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N'-hydroxy-1-methyl-5-nitro-1H-pyrazole-3-carboximidamide | HCID 136348433 | 67% |
Reaction Steps
To a solution of 1-methyl-5-nitro-1H-pyrazole-3-carbonitrile (2.4 g, 15.8 mmol, Princeton) and hydroxylamine hydrochloride (3.29 g, 47.3 mmol) in EtOH (0.50 mL) was added potassium carbonate (10.9 g, 79 mmol) and the mixture was refluxed for about 2 h. The reaction mixture was filtered hot and the collected solid was rinsed with EtOH (50 mL) and then MeOH (100 mL). The filtrate was concentrated under reduced pressure. The crude material was partitioned between DCM (40 mL) and water (20 mL). The aqueous layer was acidified to about pH 2 using 1 N HCl and back extracted with DCM (20 mL). The aqueous layer was basified using saturated NaHCO3 and the precipitate was collected by vacuum filtration and dried to afford N′-hydroxy-1-methyl-5-nitro-1H-pyrazole-3-carboximidamide (1.24 g, 4.49 mmol, 67%). LC-MS (Table 1, Method g) Rt=1.07 min, m/z 186 (M+H)+. 1H-NMR (DMSO-d6, Bruker 400 MHz) δ 9.78 (s, 1H), 7.22 (s, 1H), 5.71 (s, 2H), 4.16 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150592B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-0b48984199de4a0694894b0d151c1a8d |
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| Source note | uspto-grants-2015_10 |
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