HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(2-chloroethyl)-2-methyl-3-hydroxy-4-pyridinone → N-(4-propargylpiperazin-1-ylethyl)-2-methyl-3-hydroxy-4-pyridinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(2-chloroethyl)-2-methyl-3-hydroxy-4-pyridinone | HCID 337279 | — |
| Reactant | 1-(2-Propynyl)piperazine | HCID 14627369 | — |
| Product | N-(4-propargylpiperazin-1-ylethyl)-2-methyl-3-hydroxy-4-pyridinone | HCID 58730241 | — |
Reaction Steps
The title compound was prepared as described in Scheme D by reaction of N-(2-chloroethyl)-2-methyl-3-hydroxy-4-pyridinone (H2, Appendix VII) (prepared as described in Bijaya L. Rai, Lotfollah Dekhordi, Hicham Khodr, Yi Jin, Zudong Liu, and Robert C. Hider J. Med. Chem. 1998, 41,3347-3359) with N-propargylpiperazine (obtained as in step (iii) in Example 2):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08058442B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-194915e88a1a4046b094fe8c00e075a1 |
| Source note | uspto-grants-2011_11 |