HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(2-Methyl-1,3-dioxolan-2-yl)acetaldehyde → 3-bromo-4-(5-methyl-1H-pyrazol-1-yl)-5-nitropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(2-Methyl-1,3-dioxolan-2-yl)acetaldehyde | HCID 11007926 | — |
| Reactant | 3-Bromo-4-hydrazinyl-5-nitropyridine | HCID 86720974 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-bromo-4-(5-methyl-1H-pyrazol-1-yl)-5-nitropyridine | HCID 86720975 | — |
Reaction Steps
2-(2-methyl-1,3-dioxolan-2-yl)acetaldehyde (320 mg, 2.459 mmol) and (3-bromo-5-nitro-4-pyridyl)hydrazine (286.4 mg, 1.229 mmol) were heated under reflux in ethanol (2.864 mL) overnight. The reaction mixture was concentrated in vacuo and the residue was partitioned between DCM and a saturated aqueous sodium hydrogen carbonate solution. Combined organic extract was dried over MgSO4 and concentrated in vacuo to leave 3-bromo-4-(5-methyl-1H-pyrazol-1-yl)-5-nitropyridine as a yellow oil. (200 mg, 85%). MS (ES+) 284.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09340546B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-28d38fbbce2f4f7fbd1058e1a32f35c4 |
| Source note | uspto-grants-2016_05 |