Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397671Generated: October 30, 2026

Dabco → HCID 178424198, compound

https://huagongshe.com/reaction/1397671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDabcoHCID 9237—
ReactantSodium hydrideHCID 24758—
Reactant6-ChloropurineHCID 5359277—
Reactant(8-Methyl-2-o-tolylquinolin-3-yl)methanolHCID 57707986—
SolventAcetic AcidHCID 176—
SolventDimethyl SulfoxideHCID 679—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 178424198HCID 178424198—

Reaction Steps

Prepared according to procedure L A mixture of 6-chloropurine (110 mg, 0.71 mmol) and 1,4-diazabicyclo[2.2.2]octane (160 mg, 1.43 mmol) in DMSO (0.7 mL) was stirred at rt for 4 h and was then added via cannula to a mixture of (8-methyl-2-o-tolylquinolin-3-yl)methanol (94 mg, 0.36 mmol) and sodium hydride, 60% dispersion in mineral oil (57 mg, 1.43 mmol) in DMSO (1 mL) that had been stirred at rt for 15 min prior to the addition. The mixture was stirred at rt for 3.5 h, neutralized by the addition of glacial acetic acid, diluted with brine (15 mL), and extracted with EtOAc (3×15 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure. The resulting yellow oil was dissolved in CH2Cl2, evaporated onto silica gel (deactivated with 2M NH3 in MeOH), and purified by flash chromatography (Biotage® Si 25+M) eluting with 2 M NH3 in MeOH/CH2Cl2 (5%) to provide a white solid [PI3Kδ IC50=27 nM]. MS (APCI+) m/z=282.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901135B2
Source datasetuspto-grants-2014_12
ORD IDord-a17036174d3e4a00bef5f76f675d19aa
Source noteuspto-grants-2014_12