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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878401Generated: November 1, 2026

1-Hydroxybenzotriazole → tert-Butyl 4-(4-(3-phenylureido)benzoyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1878401

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant4-[(Phenylcarbamoyl)amino]benzoic acidHCID 231278—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventAcetonitrileHCID 6342—
Producttert-Butyl 4-(4-(3-phenylureido)benzoyl)piperazine-1-carboxylateHCID 4651162067.1%

Reaction Steps

To a solution of 4-(3-phenylureido)benzoic acid (13.5 g, 52.68 mmol) in acetonitrile (250 mL) at room temperature was added tert-butyl piperazine-1-carboxylate (11.8 g, 63.22 mmol), 1H-benzo[d][1,2,3]triazol-1-ol (21.1 g, 156.5 mmol, HOBT) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (30 g, 156.5 mmol, EDCl). The mixture was stirred at reflux temperature for 16 hours and was then concentrated under vacuum. The residue was submitted to silica chromatography (0-5% ethyl acetate in n-hexanes as eluant) to give the title compound (15.0 g). MS (ESI) m/z 425.1 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314091B2
Source datasetuspto-grants-2012_11
ORD IDord-9979c530d824497f9bec58142a923e92
Source noteuspto-grants-2012_11