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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613832Generated: October 30, 2026

Ethanol → Tris(3-[([(4-acetylphenyl)amino]carbonyl)amino]propyl)amine

https://huagongshe.com/reaction/613832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4-Acetylphenyl isocyanateHCID 99452—
ReactantTris(3-aminopropyl)amineHCID 547030—
ReactantHCID 178466763HCID 178466763—
SolventTetrahydrofuranHCID 8028—
ProductTris(3-[([(4-acetylphenyl)amino]carbonyl)amino]propyl)amineHCID 21195008—

Reaction Steps

Compound 35, FIG. 7H.35: 4-acetylphenyl isocyanate (3 g) and tris(3-aminopropyl)amine (1.06 g) in tetrahydrofuran (50 mL) were stirred for 30 min. Ethanol (100 mL) was added and the mixture was left at r.t. for overnight. Filtration gave 2.8 g of tris(3-[([(4-acetylphenyl)amino]carbonyl)amino]propyl)amine, mp 184-5° C. This diketone (0.4 g) and aminoguanidine dihydrochloride (0.29 g) were heated in methanol (3 mL) for 4 hours. Addition of ethanol (3 mL) and filtration gave 0.5 g of tris(3-[([(4-acetylphenyl)amino]carbonyl)amino]propyl)amine tris(amidinohydrazone) trihydrochloride (Compound 35) as the dihydrate ethanolate, mp 209-10° C. dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008255
Source datasetuspto-grants-1999_12
ORD IDord-6eeaef1c9f0c4aeeae02e6b6c1c9a6b9
Source noteuspto-grants-1999_12