Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044842Generated: October 27, 2026

Diisopropylethylamine → HCID 178423774, compound

https://huagongshe.com/reaction/2044842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant6-ChloropurineHCID 5359277—
Reactant(8-Methyl-2-(2-(trifluoromethyl)phenyl)quinolin-3-yl)methanamineHCID 57707817—
SolventEthanolHCID 702—
ProductHCID 178423774HCID 178423774—

Reaction Steps

Prepared according to Procedure H using (8-methyl-2-(2-(trifluoromethyl)-phenyl)quinolin-3-yl)methanamine (0.1 g, 0.316 mmol, 1 eq) in EtOH (2 mL) was treated with iPr2NEt (0.07 mL, 0.4 mmol, 1.2 eq) followed by 6-chloropurine (0.049 g, 0.317 mmol, 1 eq). After purification, N-((8-methyl-2-(2-(trifluoro-methyl)phenyl)quinolin-3-yl)methyl)-9H-purin-6-amine as yellow syrup. The yellow syrup was triturated with CH2Cl2 and filtered to provide N-((8-methyl-2-(2-(trifluoromethyl)phenyl)quinolin-3-yl)methyl)-9H-purin-6-amine [PI3Kδ IC50=91 nM] as yellow syrup. 1H NMR (DMSO-d6) δ ppm 12.93 (1 H, s), 7.98-8.31 (4 H, m), 7.90 (1 H, d, J=7.8 Hz), 7.74-7.82 (2 H, m), 7.69 (2 H, t, J=6.5 Hz), 7.59 (1 H, d, J=7.0 Hz), 7.42-7.52 (1 H, m), 4.42-4.77 (2 H, m), 2.62 (3 H, s). Mass Spectrum (ESI) m/e=435.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586739B2
Source datasetuspto-grants-2013_11
ORD IDord-586d8d9a645b4f7bbdd13aa47641d63d
Source noteuspto-grants-2013_11