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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044925Generated: November 1, 2026

Ethanol → HCID 178508334, compound

https://huagongshe.com/reaction/2044925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-ChloropurineHCID 5359277—
ReactantHCID 57708021HCID 57708021—
ProductHCID 178508334HCID 178508334—

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of 6-chloropurine (0.1109 g, 0.7175 mmol), (8-chloro-2-(2-(trifluoro-methoxy)phenyl)quinolin-3-yl)methanamine (0.2531 g, 0.7175 mmol), and N,N-diisopropylethylamine (0.2500 mL, 1.435 mmol) in ethanol (4.221 mL, 0.7175 mmol) was stirred at 75° C. After 36 h, the mixture was removed from the heat and concentrated under reduced pressure. The residue was purified by flash column chromatography on a silica gel column using 50% of CH2Cl2:MeOH:NH4OH (89:9:1) in CH2Cl2 as eluent to give N-(((8-chloro-2-(2-(trifluoromethoxy)phenyl)quinolin-3-yl)methyl)-9H-purin-6-amine as a white solid: 1H NMR (400 MHz, DMSO-d6) δ ppm 12.94 (1 H, s), 8.38 (1 H, s), 8.03-8.32 (3 H, m), 7.96-8.02 (1 H, m), 7.93 (1 H, dd, J=7.5, 0.9 Hz), 7.51-7.75 (5 H, m), 4.69 (2 H, br. s.); LC-MS (ESI) m/z 471.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586739B2
Source datasetuspto-grants-2013_11
ORD IDord-2ff51301720e47a6acfa7e187bf6de49
Source noteuspto-grants-2013_11