HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-(4-Methoxyphenyl)-N-methyl-4-(3-pyridinyl)-2-pyrimidinamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(4-Methoxyphenyl)-4-(pyridin-3-yl)pyrimidin-2-amine | HCID 14346975 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(4-Methoxyphenyl)-N-methyl-4-(3-pyridinyl)-2-pyrimidinamine | HCID 14722206 | — |
Reaction Steps
A 2.78 g portion of N-(4-methoxyphenyl)-4-(3-pyridinyl)-2-pyrimidinamine was dissolved in 30 ml of dimethylformamide. A 528 mg portion of sodium hydride (50% in oil) was added, the reaction sealed and stirred for 45 minutes. A solution of 1.70 g of methyl iodide in 2 ml of dimethylformamide was added, the sealed mixture was stirred overnight and the solvent removed. The residue was partitioned between water and chloroform. The organic phase was dried, filtered and evaporated. The residue was crystallized from ether-hexane giving 1.4 g of the desired product as yellow crystals, mp 88°-90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04788195 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-2f2344b6e32f4f67b2b3fcb828720e8a |
| Source note | uspto-grants-1988_11 |