HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Difluorophenol → HCID 57919339, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Difluorophenol | HCID 94392 | — |
| Reactant | 4,5-Dichloro-2-(tetrahydro-pyran-2-yl)-2H-pyridazin-3-one | HCID 10729262 | — |
| Reactant | HCID 57919224 | HCID 57919224 | — |
| Product | HCID 57919339 | HCID 57919339 | — |
Reaction Steps
In an analogous manner to the stepwise sequence outlined in intermediate 19, starting from 4,5-dichloro-2-(tetrahydropyran-2-yl)-2H-pyridazin-3-one (Intermediate 20) and 2,6-difluoro-phenol and alkylating with 2-bromo-3-(2,6-difluoro-phenyl)-propionic acid methyl ester (Intermediate 15) afforded 2-[4-(2,6-difluoro-phenoxy)-6-oxo-6H-pyridazin-1-yl]-3-(2,6-difluoro-phenyl)-propionic acid as a light yellow solid (1.35 g, 98% for the final step). 1H NMR (300 MHz, DMSO-d6) δ ppm 3.42 (d, J=7.6 Hz, 2H), 5.47 (t, J=7.6 Hz, 1H), 6.00 (d, J=2.7 Hz, 1H), 6.93-7.09 (m, 2H), 7.22-7.55 (m, 4H), 8.20 (d, J=2.7 Hz, 1H), 13.38 (br s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08258134B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-30c01ca9908b4792ad849d8537cb2bd4 |
| Source note | uspto-grants-2012_09 |