HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214446Generated: October 27, 2026
Acetic Acid → 3,5-Dibenzyl-2-(piperazin-1-yl)-3,5-dihydro-imidazo[4,5-c]pyridin-4-one
https://huagongshe.com/reaction/2214446
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 3,5-Dibenzyl-2-methanesulphonyl-3,5-dihydro-imidazo[4,5-c]pyridin-4-one | HCID 21947688 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3,5-Dibenzyl-2-(piperazin-1-yl)-3,5-dihydro-imidazo[4,5-c]pyridin-4-one | HCID 21947651 | 5.5% |
Reaction Steps
660 mg (11 mmol) of glacial acetic acid were added dropwise to 860 mg (10 mmol) of piperazine with cooling, then 180 mg of 3,5-dibenzyl-2-methanesulphonyl-3,5-dihydro-imidazo[4,5-c]pyridin-4-one (crude product from Example 3 h) were added and the mixture was stirred for 24 hours at 150° C. After cooling approx. 10 ml of water were added, the mixture was made alkaline with concentrated ammonia solution and the mixture was extracted three times with 5 ml of dichloromethane. The extracts were dried over sodium sulphate and concentrated by evaporation. The crude product thus obtained was purified by column chromatography (silica gel; eluant:petroleum ether with 20–60% ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07109192B2 |
|---|
| Source dataset | uspto-grants-2006_09 |
|---|
| ORD ID | ord-ca3933c2e6dc442492101b65fb3b194d |
|---|
| Source note | uspto-grants-2006_09 |
|---|