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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781133Generated: October 30, 2026

Hydrochloric Acid → 4-[(4-(Aminoiminomethyl)phenyl)amino]-4-oxobutanoic acid hydrochloride

https://huagongshe.com/reaction/1781133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantSuccinic anhydrideHCID 7922—
Reactant4-Amidinoaniline dihydrochlorideHCID 75626—
SolventAcetoneHCID 180—
SolventPyridineHCID 1049—
Product4-[(4-(Aminoiminomethyl)phenyl)amino]-4-oxobutanoic acid hydrochlorideHCID 69951943—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2.2 g of 4-aminobenzamidine dihydrochloride, 1.1 g of succinic anhydride and 10 mL of DMF was stirred at ambient temperature for 15 min at which time 0.83 mL of pyridine was added all at once. The resulting heterogeneous mixture was warmed to 100° C. and maintained at 100° C. for 1.5 h. The disappearance of starting material was monitored by an in-process check using HPLC Method B. After cooling to 0° C., a solution of 8 wt % concentrated HCl in acetone was added slowly while maintaining the temperature at 0° C. After the addition of additional acetone, the resulting milky suspension was stirred for 30 min and the solids were collected by vacuum filtration. The solids were then washed twice each with aq 0.5M HCl followed by acetone and were dried in a vacuum oven at 30°-40° C. to afford 2.4 g (88% molar yield) of the title compound. Acceptance testing was performed on the product using HPLC Method B to determine the presence of the title product. λmax (CH3OH) 281 nm; (0.1% H3PO4 in water) 203, 270 nm; IR (KBr): 1736 (C=O), 1674 (C--N, C=N), 1599 (C=N) cm-1 ; DSC endotherms at 167° C. and 275° C.; 1H NMR: (d6 -DMSO) δ 12.15 (s, 1H), 10.55 (s, 1H), 9.23 (s, 2H), 9.0 (s, 2H), 7.81 (s, 4H), 3.31 (s, 3H), 2.62 (m, 2H), 2.55 (m, 2H) ppm; 13C NMR: δ 173.6, 171.0, 164.8, 144.3, 129.1, 121.2, 118.3, 31.2, 28.6 ppm; Anal calcd for C11H14N3O3Cl.0.25 H2O: C, 47.83, H, 5.29; N, 15.21; Cl, 12.84; Found: C, 47.68; H, 5.02; N, 15.23; Cl, 12.92.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05631399
Source datasetuspto-grants-1997_05
ORD IDord-c3ffda7153b1440c87f670af1d6f0837
Source noteuspto-grants-1997_05