HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095783Generated: October 31, 2026
Hydrochloric Acid → 1-(4-Fluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile
https://huagongshe.com/reaction/2095783
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | 3-Buten-2-one, 4-methoxy- | HCID 94297 | — |
| Reactant | (3E)-4-Methoxy-3-buten-2-one | HCID 639675 | — |
| Reactant | 2-Cyano-N-(4-fluorophenyl)acetamide | HCID 693148 | — |
| Solvent | Diethylene Glycol Monomethyl Ether | HCID 8134 | — |
| Product | 1-(4-Fluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile | HCID 66968925 | 31.2% |
Reaction Steps
A solution of 2-cyano-N-(4-fluorophenyl)acetamide (15 g, 84.2 mmol), 4-methoxybut-3-en-2-one (12.6 g, 125.9 mmol) and 1,4-diazabicyclo[2.2.2]octane (9.4 g, 84.2 mmol) in 2-(2-methoxyethoxy)ethanol (150 mL) was stirred with heating at 120° C. for 5 hr. (3E)-4-Methoxybut-3-en-2-one (4.2 g, 41.9 mmol) and 1,4-diazabicyclo[2,2,2]octane (4.7 g, 41.9 mmol) were further added to the reaction mixture, and the mixture was stirred with heating at 120° C. for 1 hr. 2N Hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and filtered, and the solvent was evaporated under reduced pressure. The obtained solid was washed with ethyl acetate to give the title compound (6 g, 31%) as a pale-brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08445509B2 |
|---|
| Source dataset | uspto-grants-2013_05 |
|---|
| ORD ID | ord-6abd68b8f551418a9767a5734fd8a080 |
|---|
| Source note | uspto-grants-2013_05 |
|---|