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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174009Generated: October 27, 2026

1-Hydroxybenzotriazole → Methyl 4-(5-t-butoxycarbonylamino-pentanoylamino)-3-propylamino-benzoate

https://huagongshe.com/reaction/1174009

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—
SolventChloroformHCID 6212—
ProductMethyl 4-(5-t-butoxycarbonylamino-pentanoylamino)-3-propylamino-benzoateHCID 23155436100.3%

Reaction Steps

In chloroform (10 ml), 5-t-butoxycarbonylaminovaleric acid (574 mg), WSCI hydrochloride (690 mg), and HOBt (487 mg) were dissolved. Then, the resulting solution was stirred at room temperature for 30 minutes. The solution was added with 4-amino-3-propylaminobenzoic acid methyl (503 mg) and stirred overnight at room temperature. After completion of the reaction, the solvent was distilled off under reduced pressure and the residue was then dissolved in chloroform. After having been washed with a saturated aqueous sodium bicarbonate solution, a saturated aqueous ammonium chloride solution, and saturated saline solution, the solution was dried 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), thereby obtaining the subject compound (540 mg) as a colorless viscous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833991B2
Source datasetuspto-grants-2010_11
ORD IDord-a918201d636f4828b33f3b52bdb40e57
Source noteuspto-grants-2010_11