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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388987Generated: October 29, 2026

Bromocyclopentane → 1-cyclopentyl-1H-imidazol-2-amine

https://huagongshe.com/reaction/388987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromocyclopentaneHCID 8728—
Reactant2-NitroimidazoleHCID 10701—
ReactantHCID 68443645HCID 68443645—
Product1-cyclopentyl-1H-imidazol-2-amineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377983B2
Source datasetuspto-grants-2013_02
ORD IDord-238e12e9168949f698337cddf7720b96
Source noteuspto-grants-2013_02