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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735627Generated: November 1, 2026

Dimethylformamide → 4-[[4-(Aminoiminomethyl)phenyl]amino]-4-oxobutanoic acid

https://huagongshe.com/reaction/1735627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSuccinic anhydrideHCID 7922—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant4-Amidinoaniline dihydrochlorideHCID 75626—
SolventPyridineHCID 1049—
Product4-[[4-(Aminoiminomethyl)phenyl]amino]-4-oxobutanoic acidHCID 6995105688%

Reaction Conditions

Temperature100 °C

Reaction Steps

U.S. Pat. No. 5,344,957 discloses a process for preparing ethyl 3S 3-[[4-[[4-(aminoiminomethyl)phenyl]amino]-1,4-dioxobutyl]amino]-4-pentynoate having the following formula ##STR2## This process is described as follows: 4-Aminobenzamidine di-HCl (25 g, 120 mmol), which is commercially available, particularly from Aldrich, was added to dry DMF (100 ml). To this solution dry pyridine (100 ml) and succinic anhydride (12 g, 120 mmol) followed by dimethylaminopyridine (DMAP 1.5 g 0.012 mmol) were added. The product precipitated after heating for 1/2 h at 100° C. The product was filtered, washed with water, acetonitrile and ether. The light solid was suspended in dioxane, 4N HCl in dioxane (100 ml) was added and the suspension was stirred for 1 h, filtered and dried in a desiccator to give 28 g, 88% of 4-[[4-(aminoiminomethyl)phenyl]-amino]-4-oxobutanoic acid as a white yellow solid which decomposes between 270° C. and 290° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536869
Source datasetuspto-grants-1996_07
ORD IDord-562f7e6e215542c0ac1646e171e934b3
Source noteuspto-grants-1996_07