Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 25174611 | HCID 25174611 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 25174615 | HCID 25174615 | — |
Reaction Steps
4-[3-(3-Pyrazol-1-yl-phenyl)-imidazo[1,2-b]pyridazin-7-yl]-benzoic acid ethyl ester (Ex. 34) (1 eq, 0.073 mmol, 30 mg) and ethanol amine (10 eq, 0.73 mmol, 0.04 ml) are dissolved in EtOH (2 ml) and K2CO3 (1.5 eq, 0.11 mmol, 15.1 mg) is added. The reaction mixture is stirred for 5 h at 55° C. The solvent is then removed in vacuo and the reaction is purified by flash column chromatography eluting with 9:1 DCM/MeOH to yield N-(2-Hydroxy-ethyl)-4-[3-(3-pyrazol-1-yl-phenyl)-imidazo-[1,2-b]-pyridazin-7-yl]-benzamide as a yellow solid; [M+H]+=425
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143253B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-ccbeff6476b744f4b9841b2d3d43f1b9 |
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| Source note | uspto-grants-2012_03 |
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