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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505533Generated: October 30, 2026

Pyridine → HCID 86702970, compound

https://huagongshe.com/reaction/1505533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant5-(1,3-Dioxolan-2-yl)furan-2-sulfonyl chlorideHCID 18525922—
Reactant2,6-difluoro-N1-(3-(9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-yl)pyridin-2-yl)benzene-1,3-diamineHCID 86702947—
SolventDichloromethaneHCID 6344—
ProductHCID 86702970HCID 8670297094%

Reaction Conditions

Temperature50 °C

Reaction Steps

The 2,6-difluoro-N1-(3-(9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-yl)pyridin-2-yl)benzene-1,3-diamine (50 mg, 0.120 mmol) prepared at Step 9 was added and dissolved into dichloromethane solvent. 5-(1,3-dioxolane-2-yl)furan-2-sulfonyl chloride (24 mg, 0.130 mmol) and pyridine (11 uL, 0.130 mmol) were added into the reaction solution and stirred at 50° C. for 2 hours. After the reaction, the reactant was washed with 1N aqueous hydrochloric acid solution and salt water. After extraction with dichloromethane, the organic layer was dried with sulfuric anhydride magnesium and vacuum concentrated, and then refined by means of column chromatography, so that 71 mg of the target compound, N-(2,4-difluoro-3-(3-(9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-yl)pyridin-2-ylamino)phenyl)-5-(1,3-dioxolane-2-yl)furan-2-sulfonamide (percentage yield: 94%), was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216981B2
Source datasetuspto-grants-2015_12
ORD IDord-f1d6665c3c4e4c889e8e736b6a248833
Source noteuspto-grants-2015_12