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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510322Generated: October 25, 2026

Potassium Carbonate → 5-(4-methoxypyrimidin-2-yl)-1-methyl-1H-indazole

https://huagongshe.com/reaction/510322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-4-methoxypyrimidineHCID 588935—
Reactant1-Methyl-1H-indazole-5-boronic acidHCID 22558910—
CatalystHCID 178418397HCID 178418397—
Product5-(4-methoxypyrimidin-2-yl)-1-methyl-1H-indazoleHCID 86699854—

Reaction Conditions

Temperature185 °C

Reaction Steps

2-chloro-4-methoxypyrimidine (100.0 mg, 0.69 mmol), 1-methyl-1H-indazol-5-ylboronic acid (133.9 mg, 0.76 mmol), Pd(PPh3)4 (79.9 mg, 0.069 mmol), and K2CO3 (286.8 mg, 2.075 mmol) were taken in a microwave vial and the vial was vacuum pumped and flushed with argon three times. To this mixture was added degassed toluene (2.5 mL) and DMF (0.28 mL). The reaction mixture was heated in a microwave at 185° C. for 30 min, diluted with ethyl acetate, filtered through Celite (ethyl acetate eluent), and concentrated. Purification by flash column chromatography on silica gel (hexanes/ethyl acetate eluent) provided the product. 1H NMR (400 MHz, CDCl3) δ 8.92 (s, 1H), 8.56 (dd, J=8.9, 1.3 Hz, 1H), 8.52 (d, J=5.8 Hz, 1H), 8.10 (s, 1H), 7.47 (d, J=8.9 Hz, 1H), 6.64 (d, J=5.8 Hz, 1H), 4.14 (s, 3H), 4.12 (s, 3H). LCMS-ESI+: calc'd for C13H13N4O: 241.1 (M+H+); Found: 241.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096586B2
Source datasetuspto-grants-2015_08
ORD IDord-192c27a7d74249c4ada67dcff7654062
Source noteuspto-grants-2015_08