HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → HCID 44578630, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 44578670 | HCID 44578670 | — |
| Product | HCID 44578630 | HCID 44578630 | — |
Reaction Steps
N-(4′-{[(Cyclopropylmethyl)amino]carbonyl}-6-methyl-1,1′-biphenyl-3-yl)-2-(4-methylpiperazin-1-yl)isonicotinamide was prepared from 2-chloro-N-(4′-{[(cyclopropylmethyl)amino]carbonyl}-6-methyl-1,1′-biphenyl-3yl)isonicotinamide and N-methylpiperazine using method A. NMR; δH [2H6]—DMSO 10.31,(1H, s), 8.62,(1H, t), 8.24,(1H, d), 7.93,(2H, d), 7.71,(1H, dd), 7.64,(1H, d), 7.44,(2H, d), 7.30,(1H, d), 7.23,(1H, s), 7.06,(1H, d), 3.55,(4H, m), 3.16,(2H, t), 2.40,(4H, t), 2.21,(6H, m), 1.04,(1H, m), 0.43,(2H, m), 0.24,(2H, m). LCMS: retention time 2.74 min, MH+484.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432289B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-cdf1da84fa3f4169a4d4c405d16a3671 |
| Source note | uspto-grants-2008_10 |