HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870667Generated: November 2, 2026
Potassium Carbonate → HCID 86696367, compound
https://huagongshe.com/reaction/870667
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methoxycarbonylphenylboronic acid | HCID 2734369 | — |
| Reactant | 3-Bromo-6-(butylamino)imidazo[1,2-b]pyridazine | HCID 86696322 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Product | HCID 86696367 | HCID 86696367 | 67.3% |
Reaction Steps
To a mixture of 3-bromo-N-butylimidazo[1,2-b]pyridazin-6-amine (386 mg, 1.43 mmol), (4-(methoxycarbonyl)phenyl)boronic acid (310 mg, 1.72 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (50 mg, 0.07 mmol) and potassium carbonate (296 mg, 2.15 mmol) was added 3:1 acetonitrile/water (5 mL). The resulting mixture was heated at 145° C. (microwave) for 800 s. The reaction was then filtered and concentrated. The residue was dissolved in methanol, and then filtered again. The filtration was finally purified by column chromatography on silica gel (50% ethyl acetate in hexane) to afford methyl 4-(6-(butylamino)imidazo[1,2-b]pyridazin-3-yl)benzoate (312 mg, 67% yield) as a yellow solid: 1H NMR (CHLOROFORM-d) δ: 8.22-8.34 (m, 2H), 8.09-8.20 (m, 2H), 7.93 (s, 1H), 7.71 (d, J=9.6 Hz, 1H), 6.51 (d, J=9.6 Hz, 1H), 3.97 (s, 3H), 3.41-3.53 (m, 2H), 1.72 (t, J=7.2 Hz, 2H), 1.50 (dd, J=15.0, 7.5 Hz, 2H), 1.02 (t, J=7.5 Hz, 3H); LRMS (ESI) m/e 325.2 [(M+H)+, calcd for C18H21N4O2 325.2].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969565B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-ee6592bf9bec41a3a4792d43a46b5901 |
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| Source note | uspto-grants-2015_03 |
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