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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35056Generated: October 27, 2026

Hydrochloric Acid → 3-[[3-[(3-Amino-1-methyl-1H-1,2,4-triazol-5-yl)amino]propyl]-amino]-N,N-dimethylbenzamide

https://huagongshe.com/reaction/35056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant3-[(3-Aminopropyl)amino]-N,N-dimethylbenzamideHCID 21297566—
Reactantmethyl N-cyano-1-methyl-2-(phenylmethylene)-hydrazinecarboximidothioateHCID 54323404—
SolventAcetoneHCID 180—
Product3-[[3-[(3-Amino-1-methyl-1H-1,2,4-triazol-5-yl)amino]propyl]-amino]-N,N-dimethylbenzamideHCID 2129757042.7%

Reaction Steps

3-[(3-Aminopropyl)amino]-N,N-dimethylbenzamide (0.8 g) and N-cyano-1-methyl-2 -(phenylmethylene)hydrazine carboximidothioic acid, methyl ester eluent (0.84 g) were heated together under reduced pressure of 14 mm Hg during 4 hr at 100°. The cooled reaction mixture was dissolved in acetone, treated with 1N hydrochloric acid (2 ml) and heated at 60° for 0.5 hr. The mixture was cooled, basified with potassium carbonate and extracted with ethyl acetate. Evaporation of the organic extracts gave a viscous oil which was triturated with ether to give the title compound (0.49 g). TLC silica; methanol:ammonia (80:1) Rf 0.63. NMR (CDCl3) 2.9 m (1H); 3.2-3.7 m (3H); 5.28 t (1H); 6.12 s (2H); 6.7 s (3H); 7.0 s (6H); 6.4-7.4 m (5H); 8.23 t (2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04764612
Source datasetuspto-grants-1988_08
ORD IDord-49dc5477a30949cca4da8edda03a9b43
Source noteuspto-grants-1988_08