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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044838Generated: October 31, 2026

Triethylamine → HCID 178424197, compound

https://huagongshe.com/reaction/2044838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-6-chloropurineHCID 5360349—
Reactant(8-Methyl-2-o-tolylquinolin-3-yl)methanamineHCID 57707793—
SolventIsopropanolHCID 3776—
ProductHCID 178424197HCID 178424197—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of (8-methyl-2-o-tolylquinolin-3-yl)methanamine (40 mg, 0.15 mmol), 2-amino-6-chloropurine (52 mg, 0.30 mmol), and triethylamine (42 μL, 0.30 mmol) in i-PrOH (0.8 mL) was heated in a microwave reactor at 150° C. four times for 20 min. The mixture was partitioned between saturated aqueous NaHCO3 (15 mL) and EtOAc (15 mL), the layers were separated, and the aqueous layer was extracted with EtOAc (2×15 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, and purified by flash chroma-tography (Biotage® Si 25+M) eluting with MeOH/CH2Cl2 (5% to 10%) to provide a white solid. The compound was further purified by reversed-phase HPLC (Gilson) eluting with H2O/MeCN/TFA to provide a white solid [PI3Kδ IC50=82 nM]. MS (ESI+) m/z=396.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586739B2
Source datasetuspto-grants-2013_11
ORD IDord-ad2ef2146328451bb6dbfaa1ef13a1fb
Source noteuspto-grants-2013_11