HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-tert-Butyl-1,1,3,3-tetramethylguanidine → 3-iodo-4-nitro-1-(2-(pyridin-2-yl)ethyl)-1H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-tert-Butyl-1,1,3,3-tetramethylguanidine | HCID 3571581 | — |
| Reactant | 2-(2-Bromoethyl)pyridine hydrobromide | HCID 12913859 | — |
| Reactant | HCID 178526562 | HCID 178526562 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-iodo-4-nitro-1-(2-(pyridin-2-yl)ethyl)-1H-indazole | HCID 67976323 | 34% |
Reaction Steps
2-Tert-butyl-1,1,3,3-tetramethyl-guanidine (0.48 mL, 2.4 mmol) was added to a mixture of 3-iodo-4-nitro-1H-indazole (0.30 g, 1.0 mmol) and 2-(2-bromoethyl)pyridine hydrobromide (0.30 g, 1.1 mmol) in CH3CN (4 mL). The mixture was stirred at ambient temperature overnight, diluted with H2O (35 mL), stirred for 30 minutes, and then extracted with CHCl3. The combined organic extracts were dried over MgSO4 and concentrated. The residue was purified by silica gel chromatography, eluting with EtOAc, to provide 3-iodo-4-nitro-1-(2-(pyridin-2-yl)ethyl)-1H-indazole (0.14 mg, 34%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09174981B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-3518179b6d084d8aae756dee8c6b6544 |
| Source note | uspto-grants-2015_11 |