HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109950Generated: October 30, 2026
Potassium Hydroxide → HCID 57635774, compound
https://huagongshe.com/reaction/2109950
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 11257045 | HCID 11257045 | — |
| Reactant | Acetic acid methylene chloride | HCID 21922555 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57635774 | HCID 57635774 | 75% |
Reaction Steps
To a solution of 3-{[3-tert-butyl-1-(2,6-dimethylphenyl)-1H-pyrazol-5-yl]amino}pyridine-2-carboxylic acid (Example 10, 50 mg, 0.14 mmol) in an acetic acid/dichloromethane mixture (1 mL of each) was added N-iodosuccinimide (31 mg, 0.14 mmol). The solution was stirred at rt for 12 h, and then water (10 mL) was added. The reaction mixture was basified to pH 9 using KOH (1.0 M ice cold solution). The water layer was extracted with dichloromethane (50 mL), and the organic phase was subsequently washed with saturated sodium sulfite, brine, and concentrated to dryness. The crude material was subjected to HPLC purification to give the desired product (51 mg, 75%). 1H NMR (300 MHz, CD2Cl2) δ 9.70 (s, 1H), 9.20 (s, 1H), 8.04 (m, 1H), 7.45 (m, 1H), 7.20 (m, 2H), 7.10 (m, 2H), 2.12 (s, 6H), 1.50 (s, 9H). ES-MS m/z 490.9 (MH+); HPLC RT (min) 3.40.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07517878B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-528db48a43ad41289a243521547d01c1 |
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| Source note | uspto-grants-2009_04 |
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