HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropylamine → N-isopropyl-6-methyl-2-(methylthio)pyrimidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | 4-Chloro-6-methyl-2-(methylthio)pyrimidine | HCID 241163 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-isopropyl-6-methyl-2-(methylthio)pyrimidin-4-amine | HCID 55250529 | — |
Reaction Steps
Isopropylamine (100 mL) was added very slowly to 22.0 g (125.96 mmol) of crude 4-chloro-6-methyl-2-(methylthio)pyrimidine in 70 mL of THF in a 350 mL pressure tube. NOTE: Residual POCl3 caused smoking and bubbling, therefore the addition was done at 0° C. Once acid was quenched, an additional 50 mL of isopropylamine was added and the pressure tube was sealed. The reaction vessel was brought to 60° C. and stirred overnight. The LCMS indicate very little starting material. Solvent was evaporated leaving N-isopropyl-6-methyl-2-(methylthio)pyrimidin-4-amine as a viscous yellow oil. The crude material was taken directly to the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08247408B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-c6eb644b5fde45dabe033df837da9ab6 |
| Source note | uspto-grants-2012_08 |