HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Tolylhydrazinium(1+) chloride → 2-chloro-4-[1-(3-methylphenyl)-3-methyl-1H-pyrazol-5-yl]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Tolylhydrazinium(1+) chloride | HCID 71562 | — |
| Reactant | Ammonia hydroxide | HCID 21862953 | — |
| Reactant | HCID 53955776 | HCID 53955776 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-chloro-4-[1-(3-methylphenyl)-3-methyl-1H-pyrazol-5-yl]pyridine | HCID 11482983 | 87% |
Reaction Steps
To a mixture of 1-(2-chloroisonicotinyl)-1,3-butanedione (1.35 g, 0.068 mol) and 3-methylphenylhydrazine hydrochloride (1.30 g, 0.0082 mol) in ethanol (40 mL) was added ammonia hydroxide (0.96 mL, 0.0082 mol) dropwise. The reaction mixture was heated at reflux overnight. The solvent was removed and the residue was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over magnesium sulfate and filtered. The filtrate was concentrated and the crude was purified by chromatography on silica gel (ethyl acetate/hexane, 2:8) to give 1.68 g (87% yield) of product as a yellow oil: Anal. Calcd. for C16H14ClN3: C, 67.72; H, 4.97; N, 14.81; Cl, 12.49. Found: C, 67.91; H, 5.08; N, 14.79; Cl, 12.40.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06509361B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-4b07217005f644799ac1019134ab52a2 |
| Source note | uspto-grants-2003_01 |