HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Ethynylimidazo[1,2-b]pyridazine → HCID 178429870, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Ethynylimidazo[1,2-b]pyridazine | HCID 46838760 | — |
| Reactant | 2-(3-Iodo-4-methylphenyl)-6-(4-methyl-1H-imidazol-1-yl)-1H-benzo[d]imidazole | HCID 86709561 | — |
| Product | HCID 178429870 | HCID 178429870 | — |
Reaction Steps
The title compound was synthesized from 3-ethynylimidazo[1,2-b]pyridazine and 2-(3-iodo-4-methylphenyl)-6-(4-methyl-1H-imidazol-1-yl)-1H-benzo[d]imidazole (as prepared above) in a manner similar to that described for in Example 1. The title compound was obtained a pale yellow solid. Mp: 182-184° C.; 1H NMR (400 MHz, CD3OD) δ: 8.57 (2H, brs), 8.26 (1H, s), 7.98-8.05 (3H, m), 7.74 (1H, s), 7.68-7.70 (1H, d, J=8.4 Hz), 7.46-7.48 (2H, m), 7.42-7.44 (1H, d, J=8.4 Hz), 7.29-7.33 (1H, dd, J=4.4 and 9.2 Hz), 2.61 (3H, s), 2.31 (3H, s). HRMS (ESI-TOF+): m/z [M+H]+ calcd for C26H20N7: 430.1775. found: 430.1778.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859553B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-1f36aaf9542d457dac9014019f8f8615 |
| Source note | uspto-grants-2014_10 |