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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186804Generated: October 31, 2026

Sodium Carbonate → 1-(2,4-difluorophenyl)-4-(4-methylpyrimidin-5-yl)-1H-pyrazolo[3,4-b]pyridine

https://huagongshe.com/reaction/1186804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant5-Bromo-4-methylpyrimidineHCID 12461863—
Reactant1-(2,4-difluorophenyl)-1H-pyrazolo[3,4-b]pyridin-4-ylboronic acidHCID 66668177—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventDimethoxyethane ethanol waterHCID 86587095—
Product1-(2,4-difluorophenyl)-4-(4-methylpyrimidin-5-yl)-1H-pyrazolo[3,4-b]pyridineHCID 5660254061.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

Example 64 was prepared according to the general procedure in Example 1, except heating at 90° C. for 18 h, and using the following materials: Intermediate 63A (35.0 mg, 0.127 mmol), 5-bromo-4-methylpyrimidine (41.2 mg, 0.238 mmol), sodium carbonate (58.9 mg, 0.556 mmol), EtOH:DME:H2O (1.2:2.5:1.0 ratio) (1.0 mL) and tetrakis(triphenylphosphine) palladium(0) (17.5 mg, 0.0151 mmol). Example 64 was isolated as a white solid (25.1 mg, 60.7%). Purification was done by preparative HPLC (Condition A) using a Phenomenex Luna Axia 30×100 mm S10 column from 18% Solvent B to 100% Solvent B over 12 min, ret. T=9.2 min, followed by Biotage Silica gel chromatography on a 4 g Thompson Single Step™ silica cartridge using a linear gradient from 100% hexanes to 100% (1:1 acetone/hexanes) over 10 column volumes. 1H NMR (500 MHz, CCl3D) δ ppm 9.27 (1 H, s), 8.68-8.79 (2 H, m), 8.09 (1 H, s), 7.71 (1 H, td, J=8.62, 5.95 Hz), 7.21 (1 H, d, J=4.58 Hz), 7.13 (2 H, td, J=7.86, 5.65 Hz), 2.58 (3 H, s). LC/MS (Condition B): ret. T=3.22 min, (M+H)+ 324.13. Analytical HPLC: (Condition A): >99%, ret. T=18.26 min, (Condition B): >99%, ret. T=18.09 min, (Condition C): >99%, ret. T=12.33 min, (Condition D): >99%, ret. T=10.15 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673922B2
Source datasetuspto-grants-2014_03
ORD IDord-b2e4af70d7f342a09ec6f63d89f6b6c2
Source noteuspto-grants-2014_03