Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | PUBCHEM_16685210 | HCID 16685210 | — |
| Reactant | HCID 86696367 | HCID 86696367 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86696368 | HCID 86696368 | 7.1% |
Reaction Steps
The solution of methyl aluminum (2.0 M in hexane, 0.31 mL, 0.62 mmol) in toluene (2 mL) was cooled to 0° C. Then to the stirring solution was respectively added dropwise ethane-1,2-diamine (37.4 mg, 0.62 mmol), and the solution of methyl 4-(6-(butylamino)imidazo[1,2-b]pyridazin-3-yl)benzoate (126 mg, 0.39 mmol) in toluene (1 mL). The resulting reaction was refluxed at 110° C. overnight, and then cooled to 0° C. To the solution was added dropwise water (0.05 mL), methanol (0.2 mL) and chloroform (0.2 mL). The resulting mixture was refluxed on a steam bath for 15 m, and then filtered over sodium sulfate and concentrated. The residue was purified by preparative HPLC to afford N-(2-aminoethyl)-4-(6-(butylamino)imidazo[1,2-b]pyridazin-3-yl)benzamide acetic acid salt (5.7 mg, 4% yield) as a yellow solid: 1H NMR (METHANOL-d4) δ: 8.27-8.43 (m, J=8.6 Hz, 2H), 7.95-8.04 (m, J=8.3 Hz, 2H), 7.89 (s, 1H), 7.65 (d, J=9.6 Hz, 1H), 6.75 (d, J=9.9 Hz, 1H), 3.68 (t, J=5.9 Hz, 2H), 3.41 (t, J=7.2 Hz, 2H), 3.16 (br. s., 2H), 1.95 (br. s., 5H), 1.73 (t, J=7.1 Hz, 2H), 1.42-1.61 (m, 2H), 1.02 (t, J=7.3 Hz, 3H); LRMS (ESI) m/e 353.4 [(M+H)+, calcd for C19H25N6O 353.2].
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-409caa088314409b9abf056d29544a02 |
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| Source note | uspto-grants-2015_03 |
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