HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(6-Methylpyridin-2-yl)piperazine → 5-Cyano-1-(2,4-dimethoxybenzenesulfonyl)-3-(2-ethoxyphenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl 4-(6-methylpyridin-2-yl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(6-Methylpyridin-2-yl)piperazine | HCID 2736946 | — |
| Reactant | 5-Cyano-1-(2,4-dimethoxybenzenesulfonyl)-3-(2-ethoxyphenyl)-2-oxo-2,3-dihydro-1-H-indol-3-yl phenyl carbonate | HCID 86632804 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Cyano-1-(2,4-dimethoxybenzenesulfonyl)-3-(2-ethoxyphenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl 4-(6-methylpyridin-2-yl)piperazine-1-carboxylate | HCID 11847687 | 89.6% |
Reaction Steps
0.1 g (0.16 mmol) of intermediate 1d and 115 mg (0.65 mmol) of 1-(6-methylpyridin-2-yl)piperazine were stirred in 3 ml of DMF at 100° C. for 20 minutes. The reaction mixture was then poured into 30 ml of ice-water/K2CO3. The resulting precipitate was isolated and crystallized from a little methanol, resulting 0.1 g of the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129389B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-fdcc708212f844d6804c2c3d4b085c48 |
| Source note | uspto-grants-2012_03 |