HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoethanol → 7-(2-Hydroxy-ethyl)-3-iodo-2-phenyl-7H-pyrano[2,3-c]pyridine-4,8-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | 3-iodo-2-phenyl-7H-pyrano[2,3-c]pyridine-4,8-dione | HCID 86671019 | — |
| Reactant | 3-Iodo-7-methyl-2-phenyl-7H-pyrano[2,3-c]pyridine-4,8-dione | HCID 86671029 | — |
| Product | 7-(2-Hydroxy-ethyl)-3-iodo-2-phenyl-7H-pyrano[2,3-c]pyridine-4,8-dione | HCID 86671034 | 81% |
Reaction Steps
Following the procedure used to prepare 3-iodo-7-methyl-2-phenyl-7H-pyrano[2,3-c]pyridine-4,8-dione, 3-iodo-2-phenyl-7H-pyrano[2,3-c]pyridine-4,8-dione was reacted with 2-bromoethanol to give the title compound (45.2 mg, 81%) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ 7.76-7.73 (m, 2H), 7.65 (d, J=7.3 Hz, 1H), 7.62-7.58 (m, 3H), 6.64 (d, J=7.3 Hz, 1H), 4.93 (t, J=5.5 Hz, 1H), 4.06 (t, J=5.4 Hz, 2H), 3.67 (q, J=5.4 Hz, 211).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08546376B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-d66f6ada7ea7499dad50461363ec46fc |
| Source note | uspto-grants-2013_10 |