HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → (5-Chloro-2,6-dimethylpyrimidin-4-yl)[3-methoxy-4-(3-nitroimidazo[1,2-b]pyridazin-6-yloxy)benzyl]amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Chloro-3-nitro-imidazo(1,2-b)pyridazine | HCID 10535981 | — |
| Reactant | 4-[(5-Chloro-2,6-dimethylpyrimidin-4-ylamino)methyl]-2-methoxyphenol | HCID 22640008 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (5-Chloro-2,6-dimethylpyrimidin-4-yl)[3-methoxy-4-(3-nitroimidazo[1,2-b]pyridazin-6-yloxy)benzyl]amine | HCID 22640011 | — |
Reaction Steps
In analogy to the method described in example 1, 1.25 g (4.25 mmol) of 4-[(5-chloro-2,6-dimethyl-pyrimidin-4-ylamino)methyl]-2-methoxyphenol (from example B3), 0.86 g (4.25 mmol) of 6-chloro-3-nitroimidazo[1,2-b]pyridazine and 3.0 g (21.25 mmol) of potassium carbonate are reacted in 25 ml of dimethylformamide. After chromatography on silica gel (mobile phase: gradient toluene/dioxane 5:1 to 2:1) and crystallization from methylene chloride/methanol, 1.24 g (64%) of the title compound are isolated as a pale beige solid. m.p.: 229-232° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06818642B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-9da2c7d858df409da1a49aefead8b7f6 |
| Source note | uspto-grants-2004_11 |