HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methyloxindole → HCID 178481470, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methyloxindole | HCID 6096 | — |
| Reactant | HCID 178517063 | HCID 178517063 | — |
| Reactant | HCID 178519327 | HCID 178519327 | — |
| Product | HCID 178481470 | HCID 178481470 | — |
Reaction Steps
The title compound was synthesized according to the method described for (E)-3-((1H-indazol-5-yl)methylene)indolin-2-one, except substituting 3-iodo-1H-indazole-6-carbaldehyde (462 mg, 1.70 mmol) and 1-methylindolin-2-one (250 mg, 1.70 mmol), the title compound was obtained as a yellow-orange solid (545 mg, 80%); MS ESI 402.2 [M+H]+, calcd for [C17H12IN3O+H]+ 402.01.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08481533B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-c2e2f5803a7041f9baa030088a273710 |
| Source note | uspto-grants-2013_07 |