HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098245Generated: November 1, 2026
Diisopropylethylamine → HCID 178522480, compound
https://huagongshe.com/reaction/2098245
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | 6-Chloroimidazo[1,2-b]pyridazine-2-carboxylic acid | HCID 2794637 | — |
| Reactant | HCID 178419692 | HCID 178419692 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178522480 | HCID 178522480 | 98.4% |
Reaction Steps
A mixture of 6-chloro-imidazo[1,2-b]pyridazine-2-carboxylic acid (2.5 g), HBTU (4.41 g) and DIEA (4.0 mL) in DMF (20 mL) were stirred at room temperature for 10 minutes. To this reaction mixture was added 5-(3-trifluoromethoxy-phenyl)-1H-benzoimidazol-2-ylamine hydrobromide salt (3.78 g), and the mixture was heated at 80° C. for 30 minutes. After cooling the reaction mixture to room temperature, an aqueous sodium bicarbonate solution (200 mL) was added, and the mixture was stirred for 30 minutes. The mixture was then filtered, washed with water, dried, and purified on an 80 g pre-packaged silica gel column with a gradient of 0 to 10% 2M ammonia-methanol in DCM. 4.7 g of 6-chloro-imidazo[1,2-b]pyridazine-2-carboxylic acid [5-(3-trifluoromethoxy-phenyl)-1H-benzoimidazol-2-yl]-amide was obtained. LCMS (m/z): 473.9. 1H NMR (400 MHz, DMSO-d6) δ 12.14 (2H, br. s.) 9.08 (1H, s) 8.35 (1H, d) 7.81 (1H, s) 7.73 (1H, d) 7.47-7.65 (5H, m) 7.34 (1H, d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450354B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-d5a1dc306b6d4246bbb0587cdc710b59 |
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| Source note | uspto-grants-2013_05 |
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