Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 68544802 | HCID 68544802 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 57863429 | HCID 57863429 | 76% |
Reaction Steps
Dissolve 1-{4-[7-(6-Morpholin-4-yl-pyridin-3-yl)-imidazo[1,2-a]pyridin-3-yl]-benzyl}-3-(3-trifluoromethyl-phenyl)-urea (0.220 g, 0.435 mmol, 1.0 eq.) in DMSO (2 mL). Add K2CO3 (0.120 g, 0.870 mmol, 2.0 eq.). Add piperazine (0.150 g, 1.74 mmol, 4.0 eq.). Stir the reaction mixture at 80° C. overnight under nitrogen. Pour the reaction mixture into 40 mL of ice and filter. Purify the yellow solid by silica gel chromatography using a 0-5% MeOH/DCM gradient to give the title compound 0.170 g (0.33 mmol, 76%) as a slightly yellow solid: MS(ES), m/z 518 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07666879B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-ccbefbc843834c4c8cc054c1b3f39be4 |
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| Source note | uspto-grants-2010_02 |
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