HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Nitro-2-oxindole → HCID 22042152, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Nitro-2-oxindole | HCID 230366 | — |
| Reactant | 5-Bromo-2-oxindole | HCID 611193 | — |
| Reactant | 5-Amino-2-oxindole | HCID 2773213 | — |
| Product | HCID 22042152 | HCID 22042152 | — |
Reaction Steps
5-Bromo-2-oxindole, 5-nitro-2-oxindole and 5-amino-2-oxindole can be prepared as described in Beckett et al., Tetrahedron, 24, 6093 (1968). 5-Amino-2-oxindole can be acylated to give 5-alkanamido-2-oxindole and 5-benzamido-2-oxindole, using standard procedures.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04721712 |
| Source dataset | uspto-grants-1988_01 |
| ORD ID | ord-6127e10b7ab042f0b4ab99594b4f979b |
| Source note | uspto-grants-1988_01 |