HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(Piperazin-1-yl)furo[3,2-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Chlorofuro[3,2-c]pyridine | HCID 2779746 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(Piperazin-1-yl)furo[3,2-c]pyridine | HCID 2794808 | — |
Reaction Steps
A solution of 0.065 mol of 4-chlorofuro[3,2-c]pyridine and 5 equivalents of piperazine in 25 ml of ethanol is heated for 17 hours at 120° C. under an inert atmosphere. After cooling and concentration under reduced pressure, the residue obtained is stirred in the presence of 150 ml of water and 150 ml of dichloromethane. After decanting and extraction with dichloromethane, the organic phases are dried and filtered and then concentrated under reduced pressure, enabling the expected product to be isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06399616B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-332775058b384c42ad47dcff30773d1b |
| Source note | uspto-grants-2002_06 |