Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | HCID 178514958 | HCID 178514958 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-benzyl-1H-pyrazol-3-amine | HCID 1508616 | 32% |
Reaktionsschritte
3.1 2-(1H-Pyrazole-3-yl)-isoindole-1,3-dione (11.7 mmol) is added to a suspension of NaH (2 eq.) in DMF at 0° C. Benzylbromide (1 eq.) is added and the reaction is stirred 15 h at 50° C. The solvent is removed in vacuo. Hydrazine hydroxide (10 ml) and ethanol (20 ml) are added and the reaction is stirred 17 hours at 120° C. The precipitate is filtered and the solvent is removed in vacuo. The residue is suspended in dichloromethane and filtrated. The solvent of the filtrate is removed in vacuo. The remaining residue is purified via column chromatography (Ethyl acetate/methanol). 1-Benzyl-1H-pyrazole-3-ylamine is isolated as a yellow powder in a yield of 32%; HPLC (Method B): 2.45 min; LC-MS (Method B): 1.203 min, 174.15 (M+H+);
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08236824B2 |
|---|
| Quelldatensatz | uspto-grants-2012_08 |
|---|
| ORD ID | ord-d65f0c7dc5fa45feb0aaf321b69d9ab7 |
|---|
| Quellennotiz | uspto-grants-2012_08 |
|---|