Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Chloro-3-nitro-imidazo(1,2-b)pyridazine | HCID 10535981 | — |
| Reactant | HCID 22640023 | HCID 22640023 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22640035 | HCID 22640035 | 78% |
Reaction Steps
0.18 g (3.6 mmol) of 6-chloro-3-nitro-imidazo[1,2-b]pyridazine are added to a solution of 0.85 g (3.6 mmol) of 4-[(5-chloro-pyrimidin-4-ylamino)-methyl]-phenol (from example A14) and 2.5 g (18 mmol) of potassium carbonate in 10 ml of dry N,N-dimethylformamide and the reaction mixture is stirred at 80° C. for 3 h. The temperature is allowed to raise to room temperature and the mixture is poured into water (100 ml). The precipitate is filtered off and purified by silica gel chromatography (toluene/dioxane=2:1) to yield 1.1 g (78%) of the title compound as a beige powder of m.p. 185° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06818642B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-1301dd36784b40ceaf44e23eb0e50157 |
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| Source note | uspto-grants-2004_11 |
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