HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tris(3-aminopropyl)amine → Tris(3-[([(3,5-diacetylphenyl)amino]carbonyl)amino]propyl)amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tris(3-aminopropyl)amine | HCID 547030 | — |
| Reactant | 3,5-Diacetylphenyl isocyanate | HCID 15541285 | — |
| Reactant | Tris(3-[([(3,5-diacetylphenyl)amino]carbonyl)amino]propyl)amine hexakis(amidinohydrazone) heptahydrochloride | HCID 178466969 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tris(3-[([(3,5-diacetylphenyl)amino]carbonyl)amino]propyl)amine | HCID 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 hexa-ketone (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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06180676B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-ad4b58059e01453198229e314ad2328c |
| Source note | uspto-grants-2001_01 |