HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178418546, compound → 5-Nitro-1H-indazole-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Reactant | HCID 178526495 | HCID 178526495 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 5-Nitro-1H-indazole-3-carbonitrile | HCID 22567219 | 20.3% |
Reaction Conditions
| Temperature | 160 °C |
|---|
Reaction Steps
3-iodo-5-nitro-1H-indazole (6.9 g, 23.87 mmol) was taken up in NMP (90 mL) and copper (I) cyanide (4.28 g, 47.7 mmol) was added. The reaction was heated at 160° C. for 1 h, then cooled to rt. The reaction mixture was diluted with EtOAc and filtered through celite, rinsing with EtOAc. The filtrate was washed 2× with water and 2× with brine. The organic layer was dried over Na2SO4, filtered, and concentrated. The crude material was purified by flash column chromatography eluting with 0%-50% EtOAc/Hex. 0.91 g of 5-nitro-1H-indazole-3-carbonitrile was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08940736B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-8bd21e51ddb74fa4a8a3b9f6a7321863 |
| Source note | uspto-grants-2015_01 |