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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799839Generated: October 30, 2026

Diiodomethane → 5-Iodo-1-isopropyl-1H-pyrazole-4-carbonitrile

https://huagongshe.com/reaction/1799839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantPentyl nitriteHCID 10026—
Reactant5-amino-1-isopropyl-1H-pyrazole-4-carbonitrileHCID 17962028—
Product5-Iodo-1-isopropyl-1H-pyrazole-4-carbonitrileHCID 58204841—

Reaction Steps

Amyl nitrite (13.00 g, 111.0 mmol) was added to a suspension of 5-amino-1-isopropyl-1H-pyrazole-4-carbonitrile (1.77 g, 11.8 mmol) in Diiodomethane (56.0 mL, 695 mmol) at −10° C. in 30 min. The mixture was stirred for 30 min at room temperature and then heated at 100° C. for 2 hours. The mixture was then cooled and concentrated in high vacuum to give a residue which was partitioned between ethyl acetate and 5% Na 2S2O5. The organic layer was washed with water, 0.1% of aq HCl, water, brine, dried and concentrated in vacuum. The residue was purified on silica column eluting with 20-30% ethyl acetate in heptane. Yield 1.68 g (55%). MS (ESI+): 262.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343955B2
Source datasetuspto-grants-2013_01
ORD IDord-0de5ad4b890b4dd688c7d4a2244a03d9
Source noteuspto-grants-2013_01