HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Diisopropylethylamine → {4-[(4-{[Amino(imino)methyl](methyl)amino}butanoyl)amino]butyl}(triphenyl)phosphonium bromide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Pyrazole-1-carboxamidine monohydrochloride | HCID 2734672 | — |
| Edukt | (4-{[4-(Methylamino)butanoyl]amino}butyl)(triphenyl)phosphonium bromide | HCID 89462815 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | {4-[(4-{[Amino(imino)methyl](methyl)amino}butanoyl)amino]butyl}(triphenyl)phosphonium bromide | HCID 117774922 | — |
Reaktionsschritte
(4-{[4-(methylamino)butanoyl]amino}butyl)(triphenyl)phosphonium bromide (690 mg, 1.30 mmol) was dissolved in N,N-dimethylformamide (1.4 mL). The resultant solution was treated with 1H-pyrazole-1-carboximidamide hydrochloride (216 mg, 1.47 mmol) and N,N-diisopropylethylamine (0.27 mL, 1.54 mmol). The reaction was stirred overnight at room temperature. More 1H-pyrazole-1-carboximidamide hydrochloride and N,N-diisopropylethylamine can be added to effect further conversion. The reaction mixture in N,N-dimethylformamide was used in the purification without isolation.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09434753B2 |
| Quelldatensatz | uspto-grants-2016_09 |
| ORD ID | ord-f5fa93a8df8944bb8766fa34ca559747 |
| Quellennotiz | uspto-grants-2016_09 |