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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726715Generated: October 31, 2026

Hydrochloric Acid → Ethyl beta-[[3-[4-(aminoiminomethyl)benzyl]aminobenzoyl]amino]propanoate

https://huagongshe.com/reaction/726715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium HydroxideHCID 14923—
ReactantAmmonium ChlorideHCID 25517—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantEthyl 3-aminopropanoateHCID 419889—
Reactant3-[4-Cyanobenzyl]aminobenzoic acidHCID 19707399—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductEthyl beta-[[3-[4-(aminoiminomethyl)benzyl]aminobenzoyl]amino]propanoateHCID 86751962—

Reaction Steps

3-[4-cyanobenzyl]aminobenzoic acid (0.25 g; 1 mmol), β-alanine ethyl ester.HCl (0.15 g; 1 mmol), N,N-diisopropylethylamine (0.26 g; 2 mmoles) and benzotriazol-1-yl-oxy-tris(dimethylamino)phosphonium hexafluorophosphate (0.44 g; 1 mmol) were stirred in N,N-dimethylformamide (25 ml) at room temperature for 1 hr. The reaction mixture was taken down to dryness and the residue was redissolved in ethanol (30 ml). The solution was saturated with HCl gas and allowed to stir overnight. The mixture was taken down to dryness and the residue was redissolved in ethanol (20 ml). To this solution, ammonium chloride (1 g) and ammonium hydroxide (10 ml) were added. The reaction mixture was stirred at room temperature overnight and the solvent was removed under reduced pressure. The residue was purified by HPLC using acetonitrile/water/trifluoroacetic acid system. The desired fractions were collected and lyophilized to give 190 mg of white material. FAB-MS: MH+ =369.5

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05710166
Source datasetuspto-grants-1998_01
ORD IDord-7cabe7f0fa1240cb939f9cdd23059fa5
Source noteuspto-grants-1998_01