HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(2-Oxoindolin-6-yl)acetamide → N-(2-oxoindolin-5-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(2-Oxoindolin-6-yl)acetamide | HCID 2749839 | — |
| Reactant | 5-Amino-2-oxindole | HCID 2773213 | — |
| Product | N-(2-oxoindolin-5-yl)acetamide | HCID 11206280 | — |
Reaction Steps
According to procedure for the synthesis of N-(2-oxoindolin-6-yl)acetamide, except substituting 5-aminoindolin-2-one (50 mg, 0.34 mmol), the title compound was prepared as a beige solid (46 mg, 71%). 1H NMR (400 MHz, CDCl3) δ 7.49 (s, 1H), 7.31 (d, J=7.0 Hz, 1H), 6.83 (d, J=8.0 Hz, 1H), 3.52 (s, 2H), 2.10 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765748B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-e2ebf2e21d9940a3b15d39adc5ecf0bc |
| Source note | uspto-grants-2014_07 |