HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allylamine → N-Allyl-4-(isopropylamino)-2-(methylthio)pyrimidine-5-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | 4-(Isopropylamino)-2-(methylthio)pyrimidine-5-carboxylic acid chloride | HCID 53963650 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-Allyl-4-(isopropylamino)-2-(methylthio)pyrimidine-5-carboxamide | HCID 54231982 | 51% |
Reaction Steps
To a 0° C. suspension of 4-(isopropylamino)-2-(methylthio)pyrimidine-5-carboxylic acid chloride in 10 mL of tetrahydrofuran is added 3.5 mL (46.2 mmol) of allylamine and 20 mL of tetrahydrofuran. The reaction suspension is allowed to warm briefly to room temperature, then stored at 0° C. overnight. The reaction mixture is diluted with ethyl acetate, washed with 1N HCl, a saturated solution of sodium bicarbonate, and brine. The organic phase is dried over magnesium sulfate, filtered, and concentrated to give 2.1 g (51%) of the title compound:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07501425B1 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-161ff308cde042ffb55afce2d51f1f15 |
| Source note | uspto-grants-2009_03 |