HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 6-[4-(5-Fluoro-2-trifluoromethylbenzoyl)piperazin-1-YL]imidazo[1,2-B]pyridazine-2-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Fluoro-2-(trifluoromethyl)benzoyl chloride | HCID 2737560 | — |
| Reactant | 6-Piperazin-1-ylimidazo[1,2-b]pyridazine-2-carboxylic acid ethyl ester | HCID 66864003 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-[4-(5-Fluoro-2-trifluoromethylbenzoyl)piperazin-1-YL]imidazo[1,2-B]pyridazine-2-carboxylic acid ethyl ester | HCID 66863459 | 82% |
Reaction Steps
To a solution of 6-piperazin-1-ylimidazo[1,2-b]pyridazine-2-carboxylic acid ethyl ester (1.016 g, 3.69 mmol) and diisopropylethylamine (1.29 mL, 7.38 mmol) in anhydrous dichloromethane (20 mL) was added 5-fluoro-2-trifluoromethylbenzoyl chloride dropwise at room temperature. The reaction mixture was stirred at room temperature for 15 minutes, then diluted with dichloromethane and washed with water. The organic layer was dried and concentrated in vacuo. The title compound was obtained in 82% yield (1.365 g) after purification by column chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07547698B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-b6abe68b91a44bf38cb5c4c2c28d91ae |
| Source note | uspto-grants-2009_06 |