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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377043Generated: October 30, 2026

Tris(3-aminopropyl)amine → Tris(3-[([(3,5-diacetylphenyl)amino]carbonyl)amino]propyl)amine

https://huagongshe.com/reaction/377043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(3-aminopropyl)amineHCID 547030—
Reactant3,5-Diacetylphenyl isocyanateHCID 15541285—
ReactantTris(3-[([(3,5-diacetylphenyl)amino]carbonyl)amino]propyl)amine hexakis(amidinohydrazone) heptahydrochlorideHCID 178466969—
SolventTetrahydrofuranHCID 8028—
ProductTris(3-[([(3,5-diacetylphenyl)amino]carbonyl)amino]propyl)amineHCID 21195014—

Reaction Steps

Compound 36, FIG. 7H.36: 3,5-Diacetylphenyl isocyanate (0.4 g) and tris(3-aminopropyl)amine (0.12 g) in tetrahydrofuran (5 mL) were stirred at r.t. for 30 min. Filtration gave 0.32 g of tris(3-[([(3,5-diacetylphenyl)-amino]carbonyl)amino]propyl)amine, mp 147-8 C. This hexaketone (0.4 g) and aminoguanidine dihydrochloride (0.49 g) were heated in methanol (3 mL) for 4 hours. Addition of ethanol and filtration gave 0.58 g of tris(3-[([(3,5-diacetylphenyl)amino]carbonyl)amino]propyl)amine hexakis(amidinohydrazone) heptahydrochloride (Compound 36) as the dihydrate hemi-ethanolate, mp 250-1° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06022900
Source datasetuspto-grants-2000_02
ORD IDord-e819cc39d30d4ed98f64d7e59e96466b
Source noteuspto-grants-2000_02