HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 4-(4-bromo-1H-pyrazol-1-yl)-1-methylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(4-Bromo-1H-pyrazol-1-yl)piperidine | HCID 52191621 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-bromo-1H-pyrazol-1-yl)-1-methylpiperidine | HCID 59599418 | 51% |
Reaction Steps
To a solution of 4-(4-bromopyrazol-1-yl)piperidine (480 mg, 2.09 mmol) and triethylamine (0.295 ml, 2.1 mmol) in DMF (4 ml) was added methyl iodide (2.1 ml of a 1.0M solution in DMF, 2.1 mmol) under an inert atmosphere. The reaction was stirred at room temperature overnight, then partitioned between water and EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to give the product (260 mg), which was used without further purification. 1H NMR (400 MHz, CDCl3): 7.47 (1H, s), 7.45 (1H, s), 4.16-4.04 (1H, m), 3.09-2.92 (2H, m), 2.34 (3H, s), 2.30-2.10 (4H, m), 2.10-1.96 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08796244B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-2026211a49684f48abf8970d1e018ef3 |
| Source note | uspto-grants-2014_08 |