HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Tris(3-[([(4-acetylphenyl)amino]carbonyl)amino]propyl)amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4-Acetylphenyl isocyanate | HCID 99452 | — |
| Reactant | Tris(3-aminopropyl)amine | HCID 547030 | — |
| Reactant | HCID 178466763 | HCID 178466763 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tris(3-[([(4-acetylphenyl)amino]carbonyl)amino]propyl)amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06008255 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-6eeaef1c9f0c4aeeae02e6b6c1c9a6b9 |
| Source note | uspto-grants-1999_12 |