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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109950Generated: October 30, 2026

Potassium Hydroxide → HCID 57635774, compound

https://huagongshe.com/reaction/2109950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantN-IodosuccinimideHCID 120273—
ReactantHCID 11257045HCID 11257045—
ReactantAcetic acid methylene chlorideHCID 21922555—
SolventWaterHCID 962—
ProductHCID 57635774HCID 5763577475%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517878B2
Source datasetuspto-grants-2009_04
ORD IDord-528db48a43ad41289a243521547d01c1
Source noteuspto-grants-2009_04