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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356355Generated: October 31, 2026

Potassium Carbonate → N-(4-(1-(2-(dimethylamino)ethylamino)isoquinolin-5-yl)phenyl)-1-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/2356355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant5-Bromo-N-(2-(dimethylamino)ethyl)isoquinolin-1-amineHCID 59383934—
Reactant1-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2,3-dihydro-1H-pyrazole-4-carboxamideHCID 59383938—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(4-(1-(2-(dimethylamino)ethylamino)isoquinolin-5-yl)phenyl)-1-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamideHCID 2499927673.4%

Reaction Steps

5-Bromo-N-(2-(dimethylamino)ethyl)isoquinolin-1-amine (0.068 g, 0.2 mmol) was added to a microwave vial equipped with a stirbar, along with 1-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2,3-dihydro-1H-pyrazole-4-carboxamide (0.2 g, 0.3 mmol). Then 1,4-Dioxane (3 ml, 35 mmol) was added into the mixture, followed by 2M K2CO3 (0.5 ml). Then Fibrecat (2.93% Pd, 0.010 g) was added to the mixture. The vial was capped, then placed into CEM Microwave for 10 minutes at 120° C. with 80 Watts of power supplied through Powermax feature. The mixture was diluted with DCM and water, then collected the organic layer by extracting with DCM (3×10 ml). Combined organics, dried over Na2SO4, filtered and concentrated in-vacuo. The crude was purified by ISCO Amino-propyl chromatography using MeOH/DCM as the eluent. This gave the title compounds as a tan amorphous solid (85 mg). MS (ESI pos. ion) m/z: 579 (MH+). Calc'd exact mass for C34H38N6O3: 578.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759344B2
Source datasetuspto-grants-2010_07
ORD IDord-f3095c49e3a64405b3e1140d551411c8
Source noteuspto-grants-2010_07