HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 178481172, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 1,1-Dimethylethyl 4-(2-thiazolylamino)-1-piperidinecarboxylate | HCID 23130942 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178481172 | HCID 178481172 | 21% |
Reaction Steps
To a solution of tert-butyl 4-(1,3-thiazol-2-yl)amino-1-piperidinecarboxylate (2.5 g) obtained in Example 135b) in DMF (50 ml) was added methyl iodide (1.1 ml), and mixed at 80° C. for 4 hours. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in chloroform and an aqueous potassium carbonate solution. The organic layer was collected by separation, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was purified with silica gel column to obtain the title compound as a pale yellow solid (0.54 g, 21%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820673B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-22e9a938ba604d8d9a76c4816cd305ee |
| Source note | uspto-grants-2010_10 |