HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5521Generated: October 29, 2026
1-Methylpiperazine → HCID 178418611, compound
https://huagongshe.com/reaction/5521
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 178418684 | HCID 178418684 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178418611 | HCID 178418611 | 17.4% |
Reaction Steps
To a suspension of 2-methoxycarbonyl-4-hydroxy-5-benzyloxypyridine (18.15 g) in N-methylpiperazine (21.04 g) was heated to 100° C. for 3.5 hours. The resulting viscous solution was cooled to room temperature, diluted with a mixture of chloroform (270 ml) and methanol (30 ml) and subjected to column chromatography on silica gel (800 g). The eluate was evaporated in vacuo and the residue was purified by column chromatography on silica gel (600 g). The pure fractions were evaporated in vacuo and the residue was pulverized with diisopropyl ether to give 1-methyl-4-(4-hydroxy-5-benzyloxy-2-pyridylcarbonyl)piperazine (3.99 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05244890 |
|---|
| Source dataset | uspto-grants-1993_09 |
|---|
| ORD ID | ord-267ddbce90734d2f82315bf163cec8db |
|---|
| Source note | uspto-grants-1993_09 |
|---|