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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694586Generated: October 27, 2026

1,2-Dimethoxyethane → HCID 57557271, compound

https://huagongshe.com/reaction/1694586

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Pyridinylboronic acidHCID 2734378—
Reactant[4-amino-7-bromo-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-imidazo[4,5-c]quinolin-2-yl]methanolHCID 67281118—
CatalystHCID 178418476HCID 178418476—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductHCID 57557271HCID 5755727152.8%

Reaction Steps

To a mixture of [4-amino-7-bromo-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-imidazo[4,5-c]quinolin-2-yl]methanol (500 mg, 1.28 mmol), 3-pyridyl boronic acid (233 mg, 1.90 mmol), potassium carbonate (579 mg, 4.20 mmol), dimethoxyethane (5 mL), and water (2.5 mL) under a nitrogen atmosphere was added Pd(PPh3)2Cl2 (18 mg, 0.026 mmol). The resulting suspension was refluxed for 2 hours. The reaction was cooled to ambient temperature. The reaction mixture was diluted with chloroform and placed directly onto a silica gel column. Chromatography (SiO2, 0-40% CMA/CHCl3) gave material that was stirred in methanol and filtered to provide 263 mg of [4-amino-7-pyridin-3-yl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-imidazo[4,5-c]quinolin-2-yl]methanol as tan crystals, m.p. 260-262° C. MS (APCI) m/z 500.3 (M+H)+; Anal. calcd for C22H23N5O2: C, 67.85; H, 5.95; N, 17.98. Found: C, 67.49; H, 5.87; N, 17.83.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158794B2
Source datasetuspto-grants-2012_04
ORD IDord-cb834491d58e4420bddcf39a7ac9fb9c
Source noteuspto-grants-2012_04