HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 6-bromo-7-fluoro-3,4-dihydroquinolin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Carbostyril, 3,4-dihydro-7-fluoro- | HCID 138300 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-bromo-7-fluoro-3,4-dihydroquinolin-2(1H)-one | HCID 43457689 | — |
Reaction Steps
To a stirred solution of 7-fluoro-3,4-dihydroquinolin-2(1H)-one (122-2; 15 g, 0.090 mol) in N,N-dimethylformamide (50 mL) was added N-bromosuccinimide (19.22 g, 0.108 mol) portion wise at 0° C. Reaction mixture was allowed to stir at room temperature for 12 h. The reaction mixture was concentrated and diluted with ice cold water (150 mL) with constant stirring and the solid residue was filtered and dried to obtain the title compound. 1H NMR (400 MHz, CDCl3) δ 8.0 (bs, 1H), 7.34-7.32 (d, J=7.2 Hz, 1H), 6.59-6.57 (d, J=8.8 Hz, 1H), 2.95-2.91 (t, J=7.6 Hz, 2H), 2.65-2.61 (t, J=−7.6 Hz, 2H). MS (M+1): 245.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09073929B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-cdb67b7abcec4719baa5742932439951 |
| Source note | uspto-grants-2015_07 |