HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → [2-[4-(morpholin-4-yl)-2-nitrophenyl]vinyl]-1H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Morpholino-2-nitrobenzaldehyde | HCID 71651977 | — |
| Reactant | HCID 178419401 | HCID 178419401 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [2-[4-(morpholin-4-yl)-2-nitrophenyl]vinyl]-1H-indazole | HCID 86628211 | 90% |
Reaction Steps
(1H-Indazol-3-ylmethyl)triphenylphosphonium bromide (0.64 g, 1.3 mmol) was dissolved in methanol (8.0 mL) and the solution was added with 4-(morpholin-4-yl)-2-nitrobenzaldehyde (0.35 g, 1.5 mmol) and potassium carbonate (0.37 g, 2.7 mmol), followed by stirring at room temperature for 1 hour. The reaction mixture was added with water and the precipitated solid was collected by filtration and dried. The obtained solid was triturated in methanol to obtain (E)-3-([2-[4-(morpholin-4-yl)-2-nitrophenyl]vinyl]-1H-indazole (0.41 g, 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07605272B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-7418075d766d4dc3a193215e7e908171 |
| Source note | uspto-grants-2009_10 |