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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864109Generated: October 26, 2026

Fusaric Acid → (5-Butyl-pyridin-2-yl)-{4-[1-(4-methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yloxy]-piperidin-1-yl}-methanone

https://huagongshe.com/reaction/1864109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFusaric AcidHCID 3442—
ReactantIsopropyl chloroformateHCID 7917—
ReactantTriethylamineHCID 8471—
Reactant1-(4-Methanesulfonyl-phenyl)-4-(piperidin-4-yloxy)-1H-pyrazolo[3,4-d]pyrimidine hydrochlorideHCID 21897774—
SolventDimethylformamideHCID 6228—
Product(5-Butyl-pyridin-2-yl)-{4-[1-(4-methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yloxy]-piperidin-1-yl}-methanoneHCID 2189778514.3%

Reaction Steps

5-Butyl-pyridine-2-carboxylic acid (92 mg, 0.51 mmol) and isopropyl chloroformate (70 μL, 0.51 mmol) were dissolved in DMF and stirred at room temperature for 40 min. 1-(4-Methanesulfonyl-phenyl)-4-(piperidin-4-yloxy)-1H-pyrazolo[3,4-d]pyrimidine hydrochloride (70 mg, 0.17 mmol) and triethylamine (72 μL, 0.51 mmol) were added next and continued to stir for 24 hours. Progress of the reaction was monitored by TLC and LCMS. Removal of organic solvents in vacuo and purification by HPLC afforded Compound A125 as a white solid (13 mg, 13%). Exact mass calculated for C27H30N6O4S 534.63, found 535.20 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625906B2
Source datasetuspto-grants-2009_12
ORD IDord-7f572d388ed84b11ba5d819a9df8d77d
Source noteuspto-grants-2009_12