HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Methyl 3-(2-(tert-butylamino)-2-oxoethyl)-5-methyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-6-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-tert-butyl-2-chloroacetamide | HCID 222440 | — |
| Reactant | Methyl 5-methyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-6-carboxylate | HCID 725279 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 3-(2-(tert-butylamino)-2-oxoethyl)-5-methyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-6-carboxylate | HCID 59842876 | — |
Reaction Steps
To a suspension of methyl 5-methyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-6-carboxylate (2.69 g, 12 mmol) in CH3CN (30 mL) was added K2CO3 (2.01 g, 14.5 mmol), KI (2.0 g, 12 mmol), and N-tert-butyl-2-chloroacetamide (1.8 g, 12 mmol). The reaction mixture was refluxed overnight and quenched with H2O (150 mL). The resulting precipitate was filtered and dried to afford methyl 3-(2-(tert-butylamino)-2-oxoethyl)-5-methyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-6-carboxylate, as a solid (yield: quantitative).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08133998B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-5e4fa6b5758549dd9c5fc5155b7d8aea |
| Source note | uspto-grants-2012_03 |