HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-Chloroethyl)-4-phenylpiperazine dihydrochloride → 5-Benzyloxy-2-(2-[4-phenyl-1-piperazinyl]ethylamino)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-Chloroethyl)-4-phenylpiperazine dihydrochloride | HCID 11738055 | — |
| Reactant | 2-Amino-5-(benzyloxy)benzamide | HCID 20338142 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | 5-Benzyloxy-2-(2-[4-phenyl-1-piperazinyl]ethylamino)benzamide | HCID 20338487 | 29.5% |
Reaction Steps
1-(2-Chloroethyl)-4-phenylpiperazine dihydrochloride (3.3 g) was converted to the base and added to 1.2 g 5-Benzyloxyanthranilamide in 125 ml propanol. The solution was refluxed 3 hours, cooled, filtered, and the filtrate concentrated to dryness. The residue was chromatographed on alumina to give 0.63 g product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04060526 |
| Source dataset | uspto-grants-1977_11 |
| ORD ID | ord-c8ef1edc2f7840eda1b4d8fd7788ec77 |
| Source note | uspto-grants-1977_11 |