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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695773Generated: October 31, 2026

1,4-Dioxane → HCID 44540862, compound

https://huagongshe.com/reaction/1695773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(Pyridin-4-yl)boronic acidHCID 2734379—
ReactantN-[6-bromo-2-(tetrahydro-2H-pyran-2-yl)-2H-indazol-4-yl]-2-methyl-1,3-thiazole-4-carboxamideHCID 58255778—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 44540862HCID 4454086247.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A microwave vial was charged with N-[6-bromo-2-(tetrahydro-2H-pyran-2-yl)-2H-indazol-4-yl]-2-methyl-1,3-thiazole-4-carboxamide (50 mg), Solvias catalyst (7 mg), tripotassium phosphate (76 mg), 4-pyridinylboronic acid (15 mg), 1,4-dioxane (0.5 ml) and water (0.1 ml). The mixture was heated under microwave irradiation for a total of 60 min at 80° C. 4-Pyridinylboronic acid (15 mg) was added and the mixture was heated for 30 min at 80° C., then 30 min at 120° C. The reaction mixture was passed through a silica cartridge preconditioned with methanol, washing with methanol, then dried in vacuo. The residue was extracted with DCM/water, dried through a hydrophobic frit and dried in vacuo. The residue was dissolved in DMSO:methanol (1 ml, 1:1, v/v) and purified by MDAP (method E). Appropriate fractions were dried under a stream of nitrogen. The residue was dissolved in methanol and a few drops of 2M HCl (aq) were added and the reaction was stirred for 30 min. The reaction mixture was passed through an aminopropyl cartridge, preconditioned with methanol, washing with methanol, then dried to give title compound, (19 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163743B2
Source datasetuspto-grants-2012_04
ORD IDord-ccb0541508c74f8bb7687c659ab71cc2
Source noteuspto-grants-2012_04