HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-{[2-(Methanesulfonylamino)ethyl]amino}-4-(3-methylanilino)pyrimidine-5-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-(2-Aminoethylamino)-4-(m-tolylamino)pyrimidine-5-carboxamide | HCID 9817349 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-{[2-(Methanesulfonylamino)ethyl]amino}-4-(3-methylanilino)pyrimidine-5-carboxamide | HCID 18460848 | — |
Reaction Steps
A 114 μl portion of methanesulfonyl chloride and 205 μl of triethylamine were added to a mixture of 382 mg of 2-(2-aminoethylamino)-4-(3-methylanilino)pyrimidine-5-carboxamide with 10 ml of ethyl acetate, followed by stirring at room temperature for 3.5 hours. The reaction mixture was washed with water and saturated brine, and then the organic layer was dried over anhydrous magnesium sulfate. This was concentrated under a reduced pressure and the resulting residue was recrystallized from a mixed solvent of methanol and ethyl acetate to obtain 210 mg of 2-{[2-(methanesulfonylamino)ethyl]amino}-4-(3-methylanilino)pyrimidine-5-carboxamide (colorless crystals).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06432963B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-c1d78e4fc76549d98b5f58066eee71dc |
| Source note | uspto-grants-2002_08 |