HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 57671538, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 52987939 | HCID 52987939 | — |
| Reactant | HCID 86631269 | HCID 86631269 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57671538 | HCID 57671538 | — |
Reaction Steps
Methyl 5-(tert-butoxycarbonyl)-2-chloroisonicotinate. To a solution of 5-(tert-butoxycarbonyl)-2-chloroisonicotinic acid (1 g, 3.7 mmol) in dry DMF (10 mL) was added NaH (60% suspension in mineral oil, 0.37 g, 9.24 mmol) in small portions with stirring and cooling using an ice-bath. After addition, the reaction mixture was treated with MeI (0.524 mL, 9.24 mmol) dropwise, and then stirred at room temperature for 1 hour. The reaction mixture was poured into water and stirred at room temperature for 3 hours. The precipitate was filtered and dried in vacuo to afford the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08048894B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-a96d20c99382435eb9427de46e923c1d |
| Source note | uspto-grants-2011_11 |