HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226076Generated: October 27, 2026
Nitrogen → 8-(1-Ethyl-propyl)-2,6-dimethyl-3-(2-methyl-benzo[b]thiophen-3-yl)-imidazo[1,2-b]pyridazine
https://huagongshe.com/reaction/226076
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Bromo-2-methyl-1-benzothiophene | HCID 821864 | — |
| Reactant | 2,6-Dimethyl-8-(pentan-3-yl)imidazo[1,2-b]pyridazine | HCID 68841267 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-(1-Ethyl-propyl)-2,6-dimethyl-3-(2-methyl-benzo[b]thiophen-3-yl)-imidazo[1,2-b]pyridazine | HCID 57752647 | 33% |
Reaction Steps
217 mg of 8-(1-Ethyl-propyl)-2,6-dimethyl-imidazo[1,2-b]pyridazine (11.0 mmol), 227 mg of 3-bromo-2-methyl-benzo[b]thiophene (1.0 mmol), 26.2 mg of triphenylphosphine (0.1 mmol) and 650 mg of cesium carbonate (2.0 mmol) are placed into a reaction vial with 3 ml of dry DMF. N2 gas is bubbled in for 10 min and 34 mg of palladium acetate (0.05 mmol) is added. The reaction vial is capped with a Teflon cap and heated at 130° C. overnight. The reaction mixture is concentrated and applied onto a silica-gel chromatography column (Hexane:AcOEt:2M NH3 in MeOH=10:2:1) to give the title compound 119 mg (33%). mass spectrum (m/e): 364; 1H-NMR (CDCl3): 7.86 (m, 1H), 7.31 (m, 3H), 6.72 (s, 1H), 3.44 (m, 1H), 2.47 (s, 3H), 2.42 (s, 3H), 1.90 (m, 4H), 0.95 m, 6H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557103B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-ccd6ff5628d94ffa97ca4706f481bfc4 |
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| Source note | uspto-grants-2009_07 |
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