HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrophenol → 2-Bromo-7-(4-nitrophenoxy)thieno[3,2-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | 2-Bromo-7-chlorothieno[3,2-b]pyridine | HCID 18382774 | — |
| Reactant | 2-Bromo-7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridine | HCID 59424521 | — |
| Product | 2-Bromo-7-(4-nitrophenoxy)thieno[3,2-b]pyridine | HCID 59424461 | 48% |
Reaction Steps
Starting from the compound 41 (scheme 8) and following the procedure described above for the synthesis of compound 42 (scheme 8) but replacing 2-fluoro-4-nitrophenol for 4-nitrophenol, title compound 197 was obtained in 48% yield. LRMS (M+1) 350.9 (100%). 352.9 (100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07772247B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-9bd379743d434f18995c1b6c49f7fd14 |
| Source note | uspto-grants-2010_08 |