HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749794Generated: November 1, 2026
Piperidine → (Z)-2-[(1H-indol-3-yl)methylene]-6-methoxy-7-(morpholinomethyl)benzofuran-3(2H)-one
https://huagongshe.com/reaction/1749794
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Indole-3-Carboxaldehyde | HCID 10256 | — |
| Reactant | 6-methoxy-7-(morpholinomethyl)benzofuran-3(2H)-one | HCID 71278987 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (Z)-2-[(1H-indol-3-yl)methylene]-6-methoxy-7-(morpholinomethyl)benzofuran-3(2H)-one | HCID 71278547 | 10.9% |
Reaction Steps
A solution of 6-methoxy-7-(morpholinomethyl)benzofuran-3(2H)-one (0.079 g, 0.300 mmol) in methanol (1.2 mL) was added with 1H-indole-3-carboxaldehyde (0.0523 g, 0.300 mmol) and piperidine (0.00255 g, 0.0300 mmol), and the mixture was stirred at 60° C. for 2 hours. The reaction mixture was concentrated, and the residue was purified by silica gel column chromatography (chloroform/methanol) to obtain an orange crude product as a solid. This solid was suspended in ethyl acetate and thereby washed to obtain the objective (Z)-2-[(1H-indol-3-yl)methylene]-6-methoxy-7-(morpholinomethyl)benzofuran-3(2H)-one (0.0128 g, 10%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09156827B2 |
|---|
| Source dataset | uspto-grants-2015_10 |
|---|
| ORD ID | ord-fb352bceaaf24093a8c13178293993ec |
|---|
| Source note | uspto-grants-2015_10 |
|---|