HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49068Generated: October 26, 2026
Piperidine → 3-[5-(2-Morpholin-4-yl-ethoxy)-1H-indol-2-ylmethylene]-6-phenyl-1,3-dihydro-indol-2-one
https://huagongshe.com/reaction/49068
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 6-Phenyl-1,3-dihydro-indol-2-one | HCID 10536384 | — |
| Reactant | 5-(2-morpholin-4-yl-ethoxy)-1H-indole-2-carbaldehyde | HCID 22042109 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-[5-(2-Morpholin-4-yl-ethoxy)-1H-indol-2-ylmethylene]-6-phenyl-1,3-dihydro-indol-2-one | HCID 69586998 | 71.6% |
Reaction Steps
A mixture of 6-phenyl-2-oxindole (44 mg, 0.21 mmol), 5-(2-morpholin-4-yl-ethoxy)-1H-indole-2-carbaldehyde (58 mg, 0.21 mmol) and piperidine (0.1 mL) in ethanol (1 mL) was heated at 100° C. for 2 hours. The precipitate was collected by vacuum filtration, washed with ethanol and dried to give 70 mg (71%) of the title compound as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06706709B2 |
|---|
| Source dataset | uspto-grants-2004_03 |
|---|
| ORD ID | ord-96b2f85123af4623a8d7be6ca8d1fb88 |
|---|
| Source note | uspto-grants-2004_03 |
|---|