HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69170Generated: October 28, 2026
1,2-Dimethoxyethane → 2-Chloro-4-(3-quinolin-6-ylmethyl-imidazo[1,2-b]pyridazin-6-yl)-benzamide
https://huagongshe.com/reaction/69170
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (4-Carbamoyl-3-chlorophenyl)boronic acid | HCID 44119639 | — |
| Reactant | (6-Chloro-imidazo[1,2-b]pyridazin-3-yl)-quinoline | HCID 44206294 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-4-(3-quinolin-6-ylmethyl-imidazo[1,2-b]pyridazin-6-yl)-benzamide | HCID 44206295 | — |
Reaction Steps
A microwave tube was charged with (6-chloro-imidazo[1,2-b]pyridazin-3-yl)-quinoline (Example 14, 150 mg, 0.509 mmol), 4-carbamoyl-3-chlorophenyboronic acid (304 mg, 1.527 mmol), DME (1.6 mL) and DMF (250 μL). 2 M Na2CO3 (763 μL, 1.527 mmol) was then added, followed by tetrakis-(triphenylphosphine)-palladium (21 mg, 0.025 mmol). The RM was heated at 90° C. for 24 h. The cool reaction mixture was poured in DCM, filtered through a Celite pad and washed with water. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo. While concentrating some crystals appeared. The crystals were filtered off and dried to afford the title compound as a beige solid (tR 4.28 min (conditions 4), MH+=414.4, 1H-NMR in DMSO-d6: 8.85 (m, 1H); 8.32 (m, 1H); 8.24 (d, 1H); 8.11 (m, 1H); 8.07 (dd, 1H); 7.97 (m, 3H); 7.86 (d, 1H); 7.80 (s, 1H); 7.78 (dd, 1H); 7.70 (s, 1H); 7.61 (d, 1H); 7.51 (dd, 1H); 4.63 (s, 2H)).
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-4c7e225ba3204cfe9d9da305fd0a5988 |
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| Source note | uspto-grants-2014_09 |
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