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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110044Generated: October 27, 2026

Imidazole → 4-{[({[2-(Carbamoylmethyl)phenyl]amino}thioxomethyl)amino]methyl}piperidine carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2110044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant1,1'-ThiocarbonyldiimidazoleHCID 80264—
Reactant2-(2-Aminophenyl)acetamideHCID 278286—
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
SolventAcetonitrileHCID 6342—
Product4-{[({[2-(Carbamoylmethyl)phenyl]amino}thioxomethyl)amino]methyl}piperidine carboxylic acid tert-butyl esterHCID 86610508—

Reaction Steps

After dissolving 1-N-Boc-4-aminomethylpiperidine (869 mg, 4.06 mmol) in acetonitrile (10 mL), a solution of thiocarbonyldiimidazole (794 mg, 4.46 mmol) and imidazole (82.9 mg, 1.22 mmol) in acetonitrile (15 mL) was added dropwise in an ice bath, and the mixture was stirred at room temperature for 4 hours. After then adding 2-(2-aminophenyl)acetamide (670 mg, 4.46 mmol) thereto, the mixture was stirred overnight at 60° C. The reaction mixture was concentrated under reduced pressure and the obtained residue was purified by silica gel column chromatography (methylene chloride/methanol=65:1→49:1) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517875B2
Source datasetuspto-grants-2009_04
ORD IDord-221f31db34c942319a3cb7052eb6bed2
Source noteuspto-grants-2009_04