HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → N-(4-amino-5-chloro-2-methoxyphenyl)-4-benzylpiperazine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-(4-acetylamino-5-chloro-2-methoxyphenyl)-4-benzylpiperazine-1-carboxamide | HCID 20538750 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(4-amino-5-chloro-2-methoxyphenyl)-4-benzylpiperazine-1-carboxamide | HCID 20538744 | — |
Reaction Steps
A solution of N-(4-acetylamino-5-chloro-2-methoxyphenyl)-4-benzylpiperazine-1-carboxamide (e9) (1.4 g) in ethanol (20 ml) was refluxed for 1 hour with an aqueous (4 ml) solution of potassium hydroxide (0.6 g). The solvent was removed by evaporation and the residue extracted with ethyl acetate. Chromatography of the solution (on alumina with 5% water, in chloroform) followed by evaporation of the solvent yielded N-(4-amino-5-chloro-2-methoxyphenyl)-4-benzylpiperazine-1- carboxamide (e10).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04329344 |
| Source dataset | uspto-grants-1982_05 |
| ORD ID | ord-2fbcd36538774dfb9c828c61312512f1 |
| Source note | uspto-grants-1982_05 |