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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080715Generated: October 27, 2026

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

https://huagongshe.com/reaction/2080715

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—
ReactantMethyl 4-amino-3-(propylamino)benzoateHCID 23155569—
SolventChloroformHCID 6212—
ProductMethyl 4-(5-t-butoxycarbonylamino-pentanoylamino)-3-propylamino-benzoateHCID 2315543654.9%

Reaction Steps

In chloroform (10 ml), 5-t-butoxycarbonylamino valeric acid (574 mg), WSCI hydrochloride (690 mg), and HOBt (487 mg) were dissolved. Then, the solution was stirred at room temperature for 30 minutes. The solution was added with the compound (503 mg) obtained in Example 3-1 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 hydrogen carbonate solution, a saturated aqueous ammonium chloride solution, and a saturated saline solution, the resultant 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 numberUS07932281B2
Source datasetuspto-grants-2011_04
ORD IDord-5e352287d3f04e45a126f9644e77ddcf
Source noteuspto-grants-2011_04