HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69175Generated: October 29, 2026
Isobutylamine → (Rac)-(6-isobutylamino-imidazo[1,2-b]pyridazin-3-yl)-quinolin-6-yl-methanol
https://huagongshe.com/reaction/69175
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | (6-Chloroimidazo[1,2-b]pyridazin-3-yl)(quinolin-6-yl)methanol | HCID 87524298 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | (Rac)-(6-isobutylamino-imidazo[1,2-b]pyridazin-3-yl)-quinolin-6-yl-methanol | HCID 44208574 | — |
Reaction Steps
(rac)-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-quinolin-6-yl-methanol (Stage 1.1, 80 mg, 0.257 mmol) and KF (30 mg, 0.515 mmol) were suspended in NMP (2 mL). Isobutylamine (129 μL, 1.287 mmol) was then added and the RM was stirred at 160° C. for 7 h. The mixture was diluted with TBME and washed with water (3×). The aqueous layer was then extracted with TBME (3×). The combined layers were dried over Na2SO4, filtered and concentrated. The residue was purified by flash chromatography (Flashmaster) to afford the title compound as a yellow foam (tR 4.11 min (conditions 4), MH+=348.0, 1H-NMR in DMSO-d6: 8.86 (m, 1H); 8.32 (m, 1H); 8.02 (m, 1H); 7.94 (d, 1H); 7.80 (m, 1H); 7.61 (d, 1H); 7.51 (dd, 1H); 7.31 (s, 1H); 6.88 (t, 1Ht); 6.61 (d, 1H); 6.24 (m, 1H); 6.12 (d, 1H); 2.98 (m, 2H); 1.82 (m, 1H); 0.86 (m, 6H)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822468B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-8783c27a2cc24dc389f649d4f5c1c640 |
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| Source note | uspto-grants-2014_09 |
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