Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912070Generated: October 27, 2026

Potassium Carbonate → (6-Phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methanol

https://huagongshe.com/reaction/912070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
ReactantPhenylboronic AcidHCID 66827—
Reactant(6-Chloro-(1,2,4)triazolo(4,3-b)pyridazin-3-yl)methanolHCID 50990671—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product(6-Phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methanolHCID 57812703—

Reaction Conditions

Temperature85 °C

Reaction Steps

A suspension of (6-chloro[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methanol (0.289 mmol, 1 eq), phenylboronic acid (0.665 mmol, 2.3 eq), Pd(PPh3)4 (45.9 mg, 0.0405 mmol, 14 mol %), and K2CO3 (132 mg, 0.955 mmol, 3.3 eq) in a 4:1 ratio of dioxane (4 mL) to H2O (1 mL) was evacuated and charged with nitrogen several times. The reaction sample was then heated conventionally at 85° C. for 1 h. CH2Cl2 and H2O were added and a standard aqueous workup was performed. The crude material was purified by pTLC [Silicycle, 1000 μM, 20×20 plate], which required two developments in a 3% MeOH in EtOAc solvent system. 1H NMR (400 MHz, CDCl3): δ=1.69 (br s, 1H), 5.35 (s, 2H), 7.56-7.60 (m, 3H), 7.64 (d, J=9.6 Hz, 1H), 7.97-8.02 (m, 2H), 8.22 (d, J=9.6 Hz, 1H). MS (ES+): m/z 227.08 (100) [MH+]. HPLC: tR=2.42 min (ZQ3, polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022206B2
Source datasetuspto-grants-2011_09
ORD IDord-5a9fcf126e674068a1cbb3236f65032f
Source noteuspto-grants-2011_09