HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Morpholine → 6-bromo-3-[(morpholin-4-yl)carbonyl]-1H-indazole
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Morpholine | HCID 8083 | — |
| Edukt | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Edukt | 6-Bromo-1H-indazole-3-carboxylic acid | HCID 24728028 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 6-bromo-3-[(morpholin-4-yl)carbonyl]-1H-indazole | HCID 68181854 | — |
Reaktionsbedingungen
| Temperatur | 45 °C |
|---|
Reaktionsschritte
To a solution of 6-bromo-1H-indazole-3-carboxylic acid (500 mg, 2.07 mmol) in DMF (10 mL) was added CDI (403.62 mg, 2.49 mmol) and the reaction mixture stirred at 45° C. for 40 minutes. Morpholine (0.36 ml, 4.16 mmol) was then added and the reaction mixture stirred at RT. The reaction mixture was quenched by diluting with water. The product was extracted into EtOAc (×2) and the combined organic extracts were then washed with water and brine and dried (Na2SO4), filtered and concentrated in vacuo to give the crude (78% pure) title compound: 1H NMR (500 MHz, DMSO) delta 3.58-3.79 (6H, m), 3.96-4.13 (2H, m), 7.36 (1H, dd, J=8.59, 1.66 Hz), 7.86 (1H, d, J=1.10 Hz), 7.93 (1H, s), 13.66 (1H, br. s.); LC-MS: m/z=+311.70 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08901313B2 |
| Quelldatensatz | uspto-grants-2014_12 |
| ORD ID | ord-6a77fbb8c287432299f1dcd7d3ba975a |
| Quellennotiz | uspto-grants-2014_12 |