HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isatin → HCID 21906981, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isatin | HCID 7054 | — |
| Reactant | 4-Methylphenylhydrazine monohydrochloride | HCID 12504 | — |
| Reactant | 4-Amino-2,6-dimethylphenol | HCID 82668 | — |
| Product | HCID 21906981 | HCID 21906981 | — |
| Product | HCID 178426640 | HCID 178426640 | — |
Reaction Steps
5-Hydroxy-4,6-dimethyl-1H-indole-2,3-dione was prepared from 3,5-dimethyl-4-hydroxyaniline according to Procedure A: 1H NMR (DMSO-d6): δ 2.17 (s, 3H), 2.30 (s, 3H), 6.45 (s, 1H), 8.29 (s, 1H), 10.65 (s, 1H); ESI-MS m/z 190 (M−H)−. The isatin was combined with 4-methylphenylhydrazine hydrochloride according to Procedure H to provide the title compound in41% yield. 1H NMR (DMSO-d6): δ 2.15 (s, 3H), 2.24 (s, 3H), 2.43 (s, 3H), 6.46 (s, 1H), 7.16 (m, 4H), 7.88 (s, 1H), 10.64 (s, 1H), 12.85 (s, 1H). APCI-MS m/z 294 (M−H, 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07129253B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-7c35e49a7ba049b9b6b3133c134be226 |
| Source note | uspto-grants-2006_10 |