HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoethanol → 7-(2-Bromoethoxy)-3-cyano-6-methoxy-4-(2,3-methylenedioxyanilino)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | 3-Cyano-7-hydroxy-6-methoxy-4-(2,3-methylenedioxyanilino)quinoline | HCID 135494159 | — |
| Product | 7-(2-Bromoethoxy)-3-cyano-6-methoxy-4-(2,3-methylenedioxyanilino)quinoline | HCID 17980513 | 82% |
Reaction Steps
Using an analogous procedure to that described in Example 8, 3-cyano-7-hydroxy-6-methoxy-4-(2,3-methylenedioxyanilino)quinoline was reacted with 2-bromoethanol to give the title compound in 82% yield; NMR Spectrum: (DMSOd6) 3.88 (t, 2H), 3.94 (s, 3H), 4.51 (t, 2H), 5.96 (s, 2H), 6.8-6.93 (m, 3H), 7.34 (s, 1H), 7.8 (s, 1H), 8.42 (s, 1), 9.53 (s, 1H); Mass Spectrum: M+H+ 444.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07501516B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-cd01101c1137484d92df54c3e56ba1c6 |
| Source note | uspto-grants-2009_03 |