HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → HCID 86720181, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178470132 | HCID 178470132 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86720181 | HCID 86720181 | 73% |
Reaction Steps
To a solution of ethyl 2-mercapto-4-methyl-1,6-naphthyridine-3-carboxylate (0.22 g, 0.89 mmol, 1 eq.) in dry DMF (5 ml) was added K2CO3 (0.37 g, 2.66 mmol, 3 eq.) at 0° C. followed by the addition of ethyl iodide (0.41 g, 2.66 mmol, 3 eq.). The reaction mixture was stirred at RT for 1 h. Afterwards the mixture was poured into ice water (10 ml) and extracted with EtOAc (3×20 ml). The combined organic layers were washed with water (20 ml), brine (20 ml), dried over anhydrous Na2SO4 to provide the crude product, which was purified by CC (EtOAc/hexane 2:3) to yield ethyl 2-(ethylthio)-4-methyl-1,6-naphthyridine-3-carboxylate (0.18 g, 0.65 mmol, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09248122B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-87bfe7ff046d49c5a35aec15db996be7 |
| Source note | uspto-grants-2016_02 |