HuagongsheHuagongshe Chemistry Print Report · For research reference only
5,6-Dimethoxyindolin-2-one → HCID 178486553, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5,6-Dimethoxyindolin-2-one | HCID 222993 | — |
| Reactant | Ethylorthoformate | HCID 53630039 | — |
| Product | HCID 178486553 | HCID 178486553 | — |
Reaction Steps
As illustrated above in Scheme (A), the intermediate, 5,6-dimethoxy oxindole (I) is reacted with ethyl ortho formate (II) to provide 5,6-dimethoxy-3-hydroxymethylene oxindole (III). This oxindole (III) is then reacted with primary or secondary amines in refluxing benzene in the presence of acetic acid or toluene sulfonic acid to yield 5,6-dimethoxy-3-(substituted amino methylene) oxindoles (IV) or (V), respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04176191 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-0f88a97320c64033b9dbd7dfa764f397 |
| Source note | uspto-grants-1979_11 |