HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 3-Bromo-1-((6-methylpyridin-2-yl)methyl)-4-nitro-1H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Nitroindazole | HCID 18057 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-Chloromethyl-2-methylpyridinium chloride | HCID 76545 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Bromo-1-((6-methylpyridin-2-yl)methyl)-4-nitro-1H-indazole | HCID 67259864 | 80.3% |
Reaction Steps
4-Nitro-1H-indazole (1.0 g, 6.1 mmol) and N-bromosuccinimide (1.1 g, 6.4 mmol) were mixed with anhydrous DMF (10 mL) in a 20 mL vial. The reaction was stirred at ambient temperature for 5 minutes. KOH (1.1 g, 18.3 mmol) and 2-(chloromethyl)-6-methylpyridine hydrochloride (1.4 g, 7.6 mmol) were added to the vial and the reaction mixture was stirred for 18 hours. The product was precipitated from solution by addition of H2O (10 mL) to the reaction mixture. The solids were collected vacuum filtration, washed with H2O and dried under vacuum to afford 3-bromo-1-((6-methylpyridin-2-yl)methyl)-4-nitro-1H-indazole (1.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08841455B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-dcb6ec09e098432b8505ca359813cc51 |
| Source note | uspto-grants-2014_09 |