HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,8-Dichloro-7-methoxy-4-(4-methoxy-benzyloxy)-quinoline → 2-Chloro-6-methoxy-4-(4-methoxybenzyloxy)-8-methyl-quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,8-Dichloro-7-methoxy-4-(4-methoxy-benzyloxy)-quinoline | HCID 56605153 | — |
| Reactant | 2,4-Dichloro-6-methoxy-8-methyl-quinoline | HCID 86627750 | — |
| Product | 2-Chloro-6-methoxy-4-(4-methoxybenzyloxy)-8-methyl-quinoline | HCID 86627751 | 58% |
Reaction Steps
2-Chloro-6-methoxy-4-(4-methoxybenzyloxy)-8-methyl-quinoline 221f was synthesized from compound 220f as a white solid in 58% yield, following the procedure as described for compound 221d. 1H NMR (CDCl3, 400 MHz) δ (ppm) 2.68 (s, 3H), 3.80 (s, 3H), 3.83 (s, 3H), 5.11 (s, 2H), 6.72 (s, 1H), 6.97 (d, J=9.03 Hz, 2H), 7.15 (dd, J=3.01 Hz and J=0.96 Hz, 1H), 7.20 (d, J=3.00 Hz, 1H), 7.40 (d, J=9.03 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08377962B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-ca3a68d9d6c544d7acaec143c07a16a7 |
| Source note | uspto-grants-2013_02 |