HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Acetylpiperazine → HCID 21082718, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Acetylpiperazine | HCID 83795 | — |
| Reactant | HCID 21082719 | HCID 21082719 | — |
| Product | HCID 21082718 | HCID 21082718 | 58% |
Reaction Steps
Using an analogous procedure to that described in Example 10, 7-(3-chloropropoxy)-3-cyano-6-methoxy-4-[4-(3-methoxyprop-1-ynyl)-2,3-methylenedioxyanilino]quinoline was reacted with 1-acetylpiperazine to give the title compound in 58% yield; NMR Spectrum: (DMSOd6 and CF3CO2D at 100° C.) 2.04 (s, 3H), 2.3–2.37 (m, 2H), 3.27–3.37 (m, 9H), 3.74–3.84 (m, 4H), 3.96 (s, 3H), 4.3–4.36 (m, 4H), 6.04 (s, 2H), 6.89 (d, 1H), 6.96 (d, 1H), 7.51 (s, 1H), 7.96 (s, 1H), 8.66 (s, 1H); Mass Spectrum: M+H+ 572.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07173135B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-15cc556e4db3409c82cfaa1912b4f7b6 |
| Source note | uspto-grants-2007_02 |