HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichloro-7-methoxy-8-methylquinoline → 2-Chloro-8-methyl-7-methoxy-4-(4-methoxy-benzyloxy)-quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichloro-7-methoxy-8-methylquinoline | HCID 53400954 | — |
| Reactant | 2,8-Dichloro-7-methoxy-4-(4-methoxy-benzyloxy)-quinoline | HCID 56605153 | — |
| Product | 2-Chloro-8-methyl-7-methoxy-4-(4-methoxy-benzyloxy)-quinoline | HCID 56605159 | 50% |
Reaction Steps
2-Chloro-8-methyl-7-methoxy-4-(4-methoxy-benzyloxy)-quinoline 221b was synthesized from compound 220b as a white powder in 50% yield, following the procedure as described for compound 221d. 1H NMR (CDCl3, 376 MHz) δ (ppm) 2.60 (s, 3H), 3.85 (s, 314), 3.97 (s, 3H), 5.18 (s, 2H), 6.69 (s, 1H), 6.97 (d, J=8.57 Hz, 1H), 7.19 (d, J=8.57 Hz, 1H), 7.42 (d, J=8.57 Hz, 1H), 8.02 (d, J=8.57 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09284307B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-935b692cecdd4e63aa7ad871922d84bb |
| Source note | uspto-grants-2016_03 |