HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 69024817, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 69026153 | HCID 69026153 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 69024817 | HCID 69024817 | 85.5% |
Reaction Steps
Methyl-4-[4-[(difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate (Step 2) (6.74 g, 17.49 mmol) suspended in acetonitrile (100 mL) was cooled in an ice-bath. N-bromosuccinimide (3.27 g, 18.36 mmol) was added. After 1 hour the ice-bath was removed and after an additional 30 minutes the reaction was diluted with acetonitrile (20 mL). The precipitate was collected by filtration to provide the title compound as an off-white solid (6.94 g, 85%). 1H NMR (300 MHz, CDCl3) δ8.20 (d, J=8.7 Hz, 2H), 7.61 (q, J=7.9 Hz, 1H), 7.30 (d, J=8.7 Hz, 2H), 7.02-6.96 (m, 1H), 6.90 (app dt, J=2.4, 9.5 Hz, 1H), 6.14 (s, 1H), 5.28 (s, 2H), 3.98 (s, 3H), 2.00 (s, 3H). ES-HRMS m/z 464.0304 (M+H calcd for C21H16BrF2NO4 requires 464.0301).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07629363B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-e2db3f125a4f477594fc614038b0ab38 |
| Source note | uspto-grants-2009_12 |