HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Pyridine-2-carboximidamide hydrochloride → HCID 178515631, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Pyridine-2-carboximidamide hydrochloride | HCID 12403615 | — |
| Edukt | 4-Chloropyridine-2-carboximidamide hydrochloride | HCID 21882000 | — |
| Edukt | 6-(4-chloro-2-pyridinyl)-2-pyridin-2-yl-1H-pyrimidin-4-one | HCID 178515630 | — |
| Produkt | HCID 178515631 | HCID 178515631 | — |
Reaktionsschritte
The procedure is as described in the case of 6-(4-chloropyrid-2-yl)-2-pyrid-2-yl-pyrimidin-4-ol (ligand PM1) in Example 3 except that, instead of 2-amidinopyridine hydrochloride, the 2-amidino-4-chloropyridine hydrochloride from Example 8 is used. After recrystallisation from DMSO, 2,6-bis(4-chloropyrid-2-yl)-pyrimidin-4-ol (ligand PM5)is obtained in the form of a colourless solid. 1H-NMR (360 MHz, DMSO-d6): 12.53 (br s, 1H): 8.74 (d, J=5.0 Hz, 1H): 8.74 (s, 1H): 8.71 (d, J=5.0 Hz, 1H): 8.64 (d, J=2.3 Hz, 1H): 7.83 (dd, J=5.0, 2.3 Hz, 1H); 7.71 (dd, J=5.0, 2.3 Hz, 1H): 7.30 (s, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07612010B2 |
| Quelldatensatz | uspto-grants-2009_11 |
| ORD ID | ord-0ca89ac5282d4a8a8d087fc9c8772636 |
| Quellennotiz | uspto-grants-2009_11 |