HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → (E)-2-(2-(8-Morpholino-3-phenylimidazo[1,2-b]pyridazin-2-yl)vinyl)quinoline-5-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 8-Morpholino-3-phenylimidazo[1,2-b]pyridazine-2-carbaldehyde | HCID 117728421 | — |
| Reactant | Ethyl 2-[(diethoxyphosphinyl)methyl]-5-quinolinecarboxylate | HCID 117732530 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (E)-2-(2-(8-Morpholino-3-phenylimidazo[1,2-b]pyridazin-2-yl)vinyl)quinoline-5-carboxylic acid | HCID 117729155 | — |
Reaction Steps
A solution of compound 73d (119 mg, 0.339 mmol) in THF (6 mL) was treated with NaH (36.9 mg, 0.924 mmol) at 0° C. and the resulting mixture was allowed to warm to room temperature over 10 min. Compound 74a (95.0 mg, 0.308 mmol) was then added in one portion and the resultant mixture was heated to 55° C. for 1 h. The reaction was allowed to cool to rt, quenched with saturated sodium bicarbonate (2 mL) and extracted with DCM (10 mL). The DCM layer was separated, dried over Na2SO4, filtered, and concentrated, and the resultant residue was purified by flash column chromatography over silica gel (0-100% EtOAc/DCM) to afford compound 74b. Mass spectrum (LCMS, ESI pos.) Calcd. For C28H23N5O3 478.2 (M+H). found 478.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09193736B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-3af8d2feaf9b446fad2ab6a333e78a93 |
| Source note | uspto-grants-2015_11 |