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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080723Generated: October 27, 2026

1-Hydroxybenzotriazole → t-Butyl[4-(5-cyano-2-propylaminophenylcarbamoyl)butyl]carbamate

https://huagongshe.com/reaction/2080723

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant5-(((Tert-butoxy)carbonyl)amino)pentanoic acidHCID 545848—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-Amino-4-(propylamino)benzonitrileHCID 22380299—
SolventChloroformHCID 6212—
Productt-Butyl[4-(5-cyano-2-propylaminophenylcarbamoyl)butyl]carbamateHCID 2108451999.9%

Reaction Steps

In chloroform (31 ml), 5-t-butoxycarbonylamino valeric acid (1.57 g), WSCI hydrochloride (1.98 g), and HOBt (1.39 g) were dissolved. Then, the solution was stirred at room temperature for 30 minutes. The solution was dropped in a chloroform solution (10 ml) containing the compound (1.18 g) obtained in Example 5-2. Then, the whole was stirred at room temperature for 12 hours. After completion of the reaction, the solvent was distilled off under reduced pressure. The residue was dissolved in chloroform and then washed with a saturated aqueous sodium hydrogen carbonate solution, a saturated aqueous ammonium chloride solution, and a saturated saline solution, followed by drying with anhydrous sodium sulfate. After filtration, the solvent was distilled off under reduced pressure and the residue was then purified through silica gel column chromatography (chloroform/ethyl acetate) to remove only highly-polar components, thereby obtaining a mixture (2.52 g) containing the subject compound as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932281B2
Source datasetuspto-grants-2011_04
ORD IDord-1cfa19c5714544cfbb96f64860efe47b
Source noteuspto-grants-2011_04