HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-Methoxyphenyl)piperazine → HCID 67999114, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxindole | HCID 321710 | — |
| Reactant | HCID 68000152 | HCID 68000152 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67999114 | HCID 67999114 | — |
| Product | HCID 68000152 | HCID 68000152 | — |
Reaction Steps
5-(2-chloropropyl)-indolin-2-one was prepared from indolin-2-one according to the synthetic and working-up method of general procedure B. 5-(2-chloropropyl)-indolin-2-one (2.46 g, 0.011 mol) and 2-methoxyphenyl piperazine (1.92 g, 0.01 mol) were dissolved in 100 ml of acetonitrile, and triethyl amine (3.04 g, 0.03 mol) was added. A reaction under refluxing was allowed to proceed at an elevated temperature for 3 hours. Working up according to general procedure B gave 3.66 g of 5-(2-(4-(2-methoxyphenyl)piperazin-1-yl)propanoyl)indolin-2-one hydrochloride. The yield was 88.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08778948B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-f163800dc7e542f7b63443311780fd27 |
| Source note | uspto-grants-2014_07 |