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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505564Generated: October 30, 2026

Pyridine → HCID 86702987, compound

https://huagongshe.com/reaction/1505564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1-Methyl-1H-indole-7-sulfonyl chlorideHCID 24229740—
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 86702987HCID 86702987—

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 (20 mg, 0.047 mmol) prepared at Step 9 was added and dissolved into dichloromethane solvent. 1-methyl-1H-indole-7-sulfonyl chloride (16 mg, 0.07 mmol) and pyridine (8 uL, 0.094 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 the target compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216981B2
Source datasetuspto-grants-2015_12
ORD IDord-55202af7d21a437e82ec174670072822
Source noteuspto-grants-2015_12