HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → 2-(4-Iodo-1H-pyrazol-1-yl)-N,N-dimethylethan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 89996125 | HCID 89996125 | — |
| Product | 2-(4-Iodo-1H-pyrazol-1-yl)-N,N-dimethylethan-1-amine | HCID 64431198 | 89% |
Reaction Steps
2-(4-Iodo-1H-pyrazol-1-yl)ethyl 4-methylbenzenesulfonate (Preparation 58) (1.03 g, 2.63 mmol) was treated with dimethylamine in THF (2M, 10 mL, 20.00 mmol) and stirred at room temperature for 3 days. Solvents were removed under reduced pressure and the residue partitioned between DCM and saturated aqueous NaHCO3. The aqueous were extracted with DCM and the combined organic layers dried and concentrated. The residue was purified by silica gel column chromatography eluting with 0 to 10% MeOH in DCM to give the title compound (616 mg, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409907B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-0f59a6da925540b6afedd712003fb605 |
| Source note | uspto-grants-2016_08 |