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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164816Generated: November 1, 2026

2-[(1H-Imidazol-2-yl)methyl]aniline → 1-[2-(2-Imidazolylmethyl)-phenylthiocarbamoyl]-4-ethoxycarbonylpiperazine

https://huagongshe.com/reaction/2164816

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[(1H-Imidazol-2-yl)methyl]anilineHCID 13344903—
Reactant4-Ethoxycarbonyl-1-piperazinylthiocarbonyl chlorideHCID 13344926—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Product1-[2-(2-Imidazolylmethyl)-phenylthiocarbamoyl]-4-ethoxycarbonylpiperazineHCID 20403322—

Reaction Steps

To a suspension of 3.8 g of 2-(2-aminobenzyl)imidazole in 38 ml of tetrahydrofuran and 3.23 ml of triethylamine is added dropwise a solution of 5.5 g of 4-ethoxycarbonyl-1-piperazinyl-thiocarbonyl chloride in 10 ml of methylene chloride at room temperature. The mixture is stirred for 1 week and the suspension filtered. The filtrate is washed with first 10% aqueous potassium carbonate, then with water, dried and evaporated to dryness to give amorphous 1-[2-(2-imidazolylmethyl)phenylthiocarbamoyl]-4-ethoxycarbonylpiperazine, characterized by NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04507311
Source datasetuspto-grants-1985_03
ORD IDord-c3ca38fd5bd54faa8618860f0e45e4a1
Source noteuspto-grants-1985_03