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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717568Generated: October 29, 2026

Potassium Carbonate → HCID 89816095, compound

https://huagongshe.com/reaction/717568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
Reactant1456534-36-3HCID 89816033—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 89816095HCID 8981609591.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

The 5-chloro-1-methyl-1,4-dihydropyridazino[3,4-d]pyrimidine (310 mg), phenyl boronic acid (208 mg) and potassium carbonate (235 mg) were dissolved in toluene (10 mL) and water (1.0 mL). The reaction mixture was degassed with nitrogen for 30 minutes and Pd(PPh3)4 (98 mg) was added. The reaction mixture was again degassed with nitrogen for 20 minutes and then heated to 100° C. for 1 hour in a sealed tube. The reaction mixture was filtered through a celite pad and washed with ethyl acetate (2×20 mL). The combined filtrate was washed with water (10 mL) and brine (10 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated. The resulting crude product was purified by column chromatography using MeOH/CHCl3 (1.0:9.0) as eluent to afford 1-methyl-5-phenyl-1,4-dihydropyrimido[4,5-c]pyridazine (350 mg) as off white solid. 1H NMR (DMSO-d6): δ 3.41 (s, 3H), 3.52-3.53 (d, 2H), 6.86 (t, 1H), 7.47-7.49 (m, 3H), 7.56-7.60 (m, 2H), 8.66 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193725B2
Source datasetuspto-grants-2015_11
ORD IDord-373b0052f8b0428ca7172c17ec0a9e4d
Source noteuspto-grants-2015_11