HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748444Generated: October 31, 2026
Sulfuric Acid → 1-(5-Iodo-6-methylpyridin-2-yl)-5-methyl-1H-pyrazole-4-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1748444
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 1-(5-amino-6-methylpyridin-2-yl)-5-methyl-1H-pyrazole-4-carboxylic acid ethyl ester | HCID 86692412 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(5-Iodo-6-methylpyridin-2-yl)-5-methyl-1H-pyrazole-4-carboxylic acid ethyl ester | HCID 86692414 | 69.8% |
Reaction Steps
After concentrated sulfuric acid (20 ml) were added to 1-(5-amino-6-methylpyridin-2-yl)-5-methyl-1H-pyrazole-4-carboxylic acid ethyl ester (7.8 g) and water (80 ml) at 0° C., sodium nitrite (3.0 g) was added therein in several portions. After stirring for 0.5 hour, potassium iodide (9.96 g) was added in several portions and the mixture was stirred for 2.5 hours at room temperature. A saturated aqueous solution of sodium bicarbonate was added in several portions at 0° C. and then an aqueous solution of sodium sulfite was added and the aqueous solution was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The resulting solid was washed with ethyl acetate and n-hexane to give the titled compound (7.76 g) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150555B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-0df563de4d2c4e5faf7d28af19e17545 |
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| Source note | uspto-grants-2015_10 |
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