HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13910474, compound → N-Benzoyl-5-chloro-2-oxo-2,3-dihydro-1H-indole-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13910474 | HCID 13910474 | — |
| Reactant | HCID 13910490 | HCID 13910490 | — |
| Reactant | HCID 20194053 | HCID 20194053 | — |
| Reactant | HCID 20194058 | HCID 20194058 | — |
| Reactant | HCID 20194059 | HCID 20194059 | — |
| Reactant | HCID 20194065 | HCID 20194065 | — |
| Reactant | HCID 20194069 | HCID 20194069 | — |
| Product | N-Benzoyl-5-chloro-2-oxo-2,3-dihydro-1H-indole-1-carboxamide | HCID 13910470 | — |
Reaction Steps
Using a similar procedure, 1-(N-propionylcarbamoyl)-5-chlorooxindole, 1-(N-pivaloylcarbamoyl)-5-chlorooxindole, 1-(N-butyrylcarbamoyl)-5-fluorooxindole, 1-(N-benzoyl-carbamoyl)-5-fluorooxindole, 1-(N-acetylcarbamoyl)-5-fluorooxindole, 1-(N-benzoylcarbamoyl)-5-bromooxindole, 1-(N-i-butyrylcarbamoyl)-5-bromooxindole and 1-(N-propionylcarbamoyl)-5-bromooxindole are prepared.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04678802 |
| Source dataset | uspto-grants-1987_07 |
| ORD ID | ord-1d949a815ac64c62a177e8363d94e0ac |
| Source note | uspto-grants-1987_07 |