HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Chloro-N-(1H-pyrazol-5-yl)-3-pyridinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Pyrazol-3-ylamine | HCID 74561 | — |
| Reactant | 2-Chloronicotinoyl chloride | HCID 2774541 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Chloro-N-(1H-pyrazol-5-yl)-3-pyridinecarboxamide | HCID 20370814 | — |
Reaction Steps
175 g. of 2-chloro-3-pyridinecarboxylic acid chloride are dissolved in 750 ml. of anhydrous dioxane containing 110 g. of triethylamine. At 10°, 83 g. of 5-aminopyrazole dissolved in 100 ml. of dioxane are added dropwise with stirring. After the addition is completed, the mixture is stirred overnight at room temperature, filtered and the precipitate washed with dioxane. The solvent is removed in vacuo and the oily residue crystallized with ethyl acetate. The product, 2-chloro-N-(1H-pyrazol-5-yl)-3-pyridinecarboxamide, is recrystallized from ethyl acetate, yield: 103 g. (46%); m.p. 162.8°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04072680 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-c9f8905ed397470999528a79ab963505 |
| Source note | uspto-grants-1978_02 |