HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 5-[2-(6-Morpholin-4-ylpyrimidin-4-yl)-3-oxo-2,3-dihydro-1H-pyrazol-4-yl]pyridine-3-carbonitrile hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-(5-Bromopyridin-3-yl)-2-(6-morpholin-4-ylpyrimidin-4-yl)-1,2-dihydro-3H-pyrazol-3-one hydrochloride | HCID 70872664 | — |
| Catalyst | Zinc cyanide (Zn(CN)2) | HCID 11186 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | 5-[2-(6-Morpholin-4-ylpyrimidin-4-yl)-3-oxo-2,3-dihydro-1H-pyrazol-4-yl]pyridine-3-carbonitrile hydrochloride | HCID 70872918 | — |
Reaction Steps
100 mg (0.2 mmol) of the compound from Example 43, 20 mg (0.2 mmol) of zinc cyanide and 8 mg (0.007 mmol) of tetrakis(triphenylphosphine)palladium in 2 ml DMF are reacted at 220° C. in a single-mode microwave oven (Emrys Optimizer) for a total of 105 min. After cooling to RT, the reaction mixture is concentrated under reduced pressure and the residue is taken up in formic acid and purified by preparative HPLC (RP18 column; mobile phase: acetonitrile/water gradient with 0.1% formic acid added to the water). The resulting formate salt is converted into the hydrochloride by addition of 0.5 ml of a 4 N solution of hydrogen chloride in dioxane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524699B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-abdfca2ac9684aa8b3bd4b6990ea5e38 |
| Source note | uspto-grants-2013_09 |