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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459654Generated: October 25, 2026

Water → Di-tert-butyl 7-amino-6,8-dioxo-2,5,9,12-tetraazatridecanedioate

https://huagongshe.com/reaction/459654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPropanedioic acid, 2-amino-, 1,3-diethyl esterHCID 81272—
ReactantN-BOC-ethylenediamineHCID 187201—
SolventChloroformHCID 6212—
ProductDi-tert-butyl 7-amino-6,8-dioxo-2,5,9,12-tetraazatridecanedioateHCID 18442407—

Reaction Steps

A solution of diethyl 2-aminomalonate (1.68 g) and tert-butyl (2-aminoethyl)carbamate (3.20 g) in dehydrated chloroform (5 ml) was stirred under reflux. After 7 hours, additional tert-butyl (2-aminoethyl)carbamate (3.20 g) was added to the reaction mixture, and the mixture was stirred under reflux for 2 days. To the reaction mixture was added water, and the solution was washed with a mixed solvent of hexane and diisopropyl ether (1:1). The aqueous layer was extracted with methylene chloride. The organic layer was washed with water and extracted with 5% aqueous citric acid solution. The aqueous layer was washed with diethyl ether and basified with sodium hydroxide. The aqueous solution was extracted with methylene chloride. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was triturated with a mixed solvent of diisopropyl ether and diethyl ether to give di-tert-butyl 7-amino-6,8-dioxo-2,5,9,12-tetraazatridecanedioate (1.87 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192943B2
Source datasetuspto-grants-2007_03
ORD IDord-087d35306bc54ab79cf4facf31ca8757
Source noteuspto-grants-2007_03