HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 5-(2,4-Dimethylphenyl)-2-(dipropylamino)-3-methylpyrimidin-4(3H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | 5-(2,4-Dimethylphenyl)-3-methyl-2-propylaminopyrimidin-4(3H)-one | HCID 58938591 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-(2,4-Dimethylphenyl)-2-(dipropylamino)-3-methylpyrimidin-4(3H)-one | HCID 58938603 | 65% |
Reaction Steps
To a solution containing 0.2 g (0.74 mmol) of 5-(2,4-dimethylphenyl)-3-methyl-2-propylaminopyrimidin-4(3H)-one in 5 ml of tetrahydrofuran under a nitrogen atmosphere was added 0.12 g (2.2 mmol) of potassium hydroxide followed by 0.38 g (2.2 mmol) of 1-iodopropane. The reaction was allowed to stir at room temperature for 12 h, diluted with ethyl acetate and washed with saturated sodium bicarbonate. The organic phase was dried over magnesium sulfate. Filtration, removal of solvent and purification of the residue via Biotage chromatography eluting with 30% ethyl acetate/dichloromethane gave 0.15 g (65%) of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897607B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-edc5335269fa4645afc010d164350cc9 |
| Source note | uspto-grants-2011_03 |