HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → HCID 54493330, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 54357563 | HCID 54357563 | — |
| Product | HCID 54493330 | HCID 54493330 | — |
Reaction Steps
By substituting N-phenylpiperazine for N-methylpiperazine in Example 1 b and the resulting 4-chloro-2-methyl-6-(4-phenyl-1-piperazinyl)-5-nitropyridine-3-carboxylic acid ethyl ester is processed as described in Example 1 c-e, 7-methyl-5-(4-phenyl-1piperazinyl)pyrido[3,4-b]pyrazine-8-carboxylic acid ethyl ester is formed, m.p. 85°-87° (ligroin).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04022779 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-0a9258bc840d4309b340d9a820844a66 |
| Source note | uspto-grants-1977_05 |