HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-4-cyanopyridine → HCID 18677150, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-4-cyanopyridine | HCID 568638 | — |
| Reactant | 4-(3,5-Bis(trifluoromethyl)-1H-pyrazol-1-yl)aniline | HCID 2740668 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 18677150 | HCID 18677150 | 54.8% |
Reaction Conditions
| Temperature | 125 °C |
|---|
Reaction Steps
A mixture of 1-(4′-aminophenyl)-3,5-bis(trifluoromethyl)pyrazole (0.36 g) and 2-chloro-4-cyanopyridine (0.14 g) in dioxane (1 mL) was heated at 125° C. in a sealed tube for 5 days. The mixture was diluted with ethyl acetate and washed with water. The organic phase was dried, filtered and evaporated. Chromatography of the residue over silica gel (methylene chloride to 2% ethanol/methylene chloride gradient gave the above-named compound (0.22 g) mp 152-153° C. NMR (CDCl3) 8.45 (1H, m), 7.86 (3H, m), 7.48 (2H, d), 7.20 (1H, br s), 7.07 (1H, s), 6.91 (1H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06506747B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-75206f775d2343318e1bbd2630cf48e5 |
| Source note | uspto-grants-2003_01 |