HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → 1,3-DIHYDRO-5-[2-(4-PHENYLPIPERAZIN-1-YL)ACETYL)-1-METHYL-2H-PYRROLO[2,3-b]PYRIDIN-2-ONE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 19079294 | HCID 19079294 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1,3-DIHYDRO-5-[2-(4-PHENYLPIPERAZIN-1-YL)ACETYL)-1-METHYL-2H-PYRROLO[2,3-b]PYRIDIN-2-ONE | HCID 19079312 | 78% |
Reaction Steps
Add 63 mg (3.9×10-4 mol) of N-phenylpiperazine and then, very slowly, 0.08 ml (5.57×10-4 mol) of triethylamine to a previously prepared solution of 100 mg (3.72×10-4 mol) of 1,3-dihydro-5-bromoacetyl-1-methyl-2H-pyrrolo[2,3-b]pyridin-2-one (Preparation 19) in 3 ml of dioxane. After 30 minutes' stirring at room temperature, the resulting precipitate is removed by filtration and the flitrate is concentrated under reduced pressure to obtain the title product in a yield of 78%. ##STR75##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05618819 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-d6d23a4020aa4a00a328ab8bc5be6add |
| Source note | uspto-grants-1997_04 |