Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220575Generated: November 3, 2026

Potassium Carbonate → {4-[4-(1,3,5-Trimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl-3'-yl]-phenyl}-methanol hydrochloride

https://huagongshe.com/reaction/220575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Hydroxymethyl)benzeneboronic acidHCID 2734706—
Reactant3'-Chloro-4-(1,3,5-trimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazineHCID 86641659—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
Product{4-[4-(1,3,5-Trimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl-3'-yl]-phenyl}-methanol hydrochlorideHCID 68594667—

Reaction Conditions

Temperature120 °C

Reaction Steps

Stir together 4-(hydroxymethyl)benzeneboronic acid (182 mg, 1.2 mmol), 3′-chloro-4-(1,3,5-trimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl (321 mg, 1.0 mmol), potassium carbonate (332 mg, 2.4 mmol) and tetrakis(triphenylphosphine)palladium(0) (58 mg, 5 μmol) in dry N,N-dimethylacetamide (4 mL) and water (2 mL) at room temperature. Heat to 120° C. for 6 hr. under nitrogen. Cool to room temperature, purify using SCX chromatography and further purify using silica gel chromatography eluting with (5:95 to 20:80 methanol:DCM). Dissolve in acetonitrile, and add 2 M aq. HCl and water then lyophilize to give the title compound as a peach coloured powder (405 mg, 94%). MS (ES): m/z=393 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202873B2
Source datasetuspto-grants-2012_06
ORD IDord-3246749354a549198d6a1fc0ed138a28
Source noteuspto-grants-2012_06