Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460078Generated: November 1, 2026

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

https://huagongshe.com/reaction/1460078

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 numberUS05854289
Source datasetuspto-grants-1998_12
ORD IDord-afbe0b61f9c749e182bd384fe71a5e5a
Source noteuspto-grants-1998_12