Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53178Generated: October 28, 2026

1-Phenylpiperazine → 1,3-DIHYDRO-5-[2-(4-PHENYLPIPERAZIN-1-YL)ACETYL)-1-METHYL-2H-PYRROLO[2,3-b]PYRIDIN-2-ONE

https://huagongshe.com/reaction/53178

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantTriethylamineHCID 8471—
ReactantHCID 19079294HCID 19079294—
Solvent1,4-DioxaneHCID 31275—
Product1,3-DIHYDRO-5-[2-(4-PHENYLPIPERAZIN-1-YL)ACETYL)-1-METHYL-2H-PYRROLO[2,3-b]PYRIDIN-2-ONEHCID 1907931278%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618819
Source datasetuspto-grants-1997_04
ORD IDord-d6d23a4020aa4a00a328ab8bc5be6add
Source noteuspto-grants-1997_04