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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879396Generated: October 27, 2026

Potassium Carbonate → 5-(5-chloropyridazin-3-yl)-1-methyl-1H-indazole

https://huagongshe.com/reaction/879396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-DichloropyridazineHCID 19959687—
Reactant1-Methyl-1H-indazole-5-boronic acidHCID 22558910—
CatalystHCID 178418397HCID 178418397—
Product5-(5-chloropyridazin-3-yl)-1-methyl-1H-indazoleHCID 86700203—

Reaction Conditions

Temperature95 °C

Reaction Steps

3,5-dichloropyridazine (200 mg, 1.34 mmol), 1-methyl-1H-indazole-5-boronic acid (260 mg, 1.48 mmol), K2CO3 (556.6 mg, 4.03 mmol), and tetrakis(triphenylphosphine)palladium(0) (233, 0.20 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 1,4-dioxane (10 mL) and degassed water (2.5 mL). The reaction mixture was heated at 95° C. for 2 h then cooled to room temperature. The reaction mixture was filtered through Celite (ethyl acetate eluent) and concentrated. Purification by flash column chromatography on silica gel (hexanes/ethyl acetate eluent) provided the product. LCMS-ESI+: calc'd for C14H10ClN4: 245.1 (M+H+); Found: 245.2 (M+H+). 1H NMR (400 MHz, Chloroform-d) δ 9.15 (d, J=2.2 Hz, 1H), 8.44 (s, 1H), 8.21 (dd, J=8.8, 1.5 Hz, 1H), 8.11 (s, 1H), 7.97 (s, 1H), 7.56 (d, J=8.8 Hz, 1H), 4.14 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987250B2
Source datasetuspto-grants-2015_03
ORD IDord-93210446a980437181a609f7022fb7f9
Source noteuspto-grants-2015_03