HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870698Generated: November 1, 2026
Potassium Carbonate → [3-(4-Aminomethyl-phenyl)-7-methyl-imidazo[1,2-b]pyridazin-6-yl]-butyl-amine
https://huagongshe.com/reaction/870698
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Aminomethylphenylboronic acid hydrochloride | HCID 2734311 | — |
| Reactant | (3-Bromo-7-methyl-imidazo[1,2-b]pyridazin-6-yl)-butyl-amine | HCID 86696400 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Product | [3-(4-Aminomethyl-phenyl)-7-methyl-imidazo[1,2-b]pyridazin-6-yl]-butyl-amine | HCID 86696399 | — |
Reaction Steps
A mixture of (3-bromo-7-methyl-imidazo[1,2-b]pyridazin-6-yl)-butyl-amine (115 mg, 0.41 mmol), (4-aminomethylphenyl)boronic acid hydrochloride (99.9 mg, 0.53 mmol), K2CO3 (170 mg, 1.23 mmol) and dichlorobis(triphenylphosphine)palladium(II) (14.4 mg, 0.021 mmol) in MeCN/water (3.2 ml/0.8 ml) was heated in a microwave at 150° C. for 15 min. The reaction mixture was diluted with MeCN and filtered. The filtrate was subjected to preparative HPLC to give the titled compound as AcOH salt (66.5 mg). 1H NMR (400 MHz, METHANOL-d4) δ ppm 1.01 (t, J=7.39 Hz, 3H) 1.42-1.52 (m, 2H) 1.73 (t, J=7.28 Hz, 2H) 2.23 (s, 3H) 3.41 (t, J=7.28 Hz, 2H) 4.16 (s, 2H) 7.44 (s, 1H) 7.52 (d, J=8.38 Hz, 2H) 7.75 (s, 1H) 8.25 (d, J=8.38 Hz, 2H) 8.54 (s, 1H). LRMS (ESI) m/z 310.2 [(M+H)]+, calc'd for C18H23N5: 309.42.
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-c36572519994400e9f3edd86eed7e1e9 |
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| Source note | uspto-grants-2015_03 |
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