HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromocyclopentane → 1-cyclopentyl-1H-imidazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromocyclopentane | HCID 8728 | — |
| Reactant | 2-Nitroimidazole | HCID 10701 | — |
| Reactant | HCID 68443645 | HCID 68443645 | — |
| Product | 1-cyclopentyl-1H-imidazol-2-amine | HCID 67378691 | — |
Reaction Steps
Bromocyclopentane (14 mmol) and 2-nitroimidazole (10 mmol) were used to prepare 1-cyclopentyl-2-nitro-1H-imidazole following the alkylation procedure described for Example 181. The product, thus obtained was reduced under hydrogenation conditions as described in general procedure F to afford 1-cyclopentyl-2-amino-1H-imidazole. This aminoimidazole derivative was converted to 1-cyclopentyl-2-isothiocyanato-1H-imidazole following the general procedure A.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820821B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-e67cfc5bba4348aca7b7300c558d75ca |
| Source note | uspto-grants-2010_10 |