HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diiodomethane → 5-iodo-1-(2-methylpropyl)-2-propyl-1H-imidazole-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | 5-amino-1-(2-methylpropyl)-2-propyl-1H-imidazole-4-carbonitrile | HCID 58500135 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-iodo-1-(2-methylpropyl)-2-propyl-1H-imidazole-4-carbonitrile | HCID 58500134 | 75% |
Reaction Steps
A solution of isoamylnitrite (6.1 mL, 45 mmol) and diiodomethane (20 mL) was heated at 85° C. under a nitrogen atmosphere. A solution of 5-amino-1-(2-methylpropyl)-2-propyl-1H-imidazole-4-carbonitrile (2.50 g, 12.1 mmol) in chloroform (60 mL) was added over a period of 30 minutes. The temperature reached 70° C. during the addition. The reaction was heated for an additional 15 minutes, allowed to cool to room temperature, and concentrated under reduced pressure. The residue was purified by suction filter chromatography on silica gel (eluting with a gradient of 10% to 25% ethyl acetate in hexane) to provide 2.88 g (75%) of 5-iodo-1-(2-methylpropyl)-2-propyl-1H-imidazole-4-carbonitrile as an orange oil that crystallized upon standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08168802B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-8c0043c3270848b99d02c4ffe5ab2510 |
| Source note | uspto-grants-2012_05 |