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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430935Generated: November 1, 2026

HCID 178418546, compound → 5-Nitro-1H-indazole-3-carbonitrile

https://huagongshe.com/reaction/1430935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178418546HCID 178418546—
ReactantHCID 178526495HCID 178526495—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product5-Nitro-1H-indazole-3-carbonitrileHCID 2256721920.3%

Reaction Conditions

Temperature160 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940736B2
Source datasetuspto-grants-2015_01
ORD IDord-8bd21e51ddb74fa4a8a3b9f6a7321863
Source noteuspto-grants-2015_01