HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 19867087, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Nanterinone | HCID 71305 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 19867087 | HCID 19867087 | — |
Reaction Steps
To a stirred suspension of 8-methyl-6-(2,4-dimethylimidazol-1-yl)-2-(1H)-quinolone (0.5 g) in chloroform (10 cm3) was added N-bromosuccinimide (NBS) (0.374 g) at room temperature. After 5 minutes the reaction mixture was evaporated to dryness and the residue chromatographed on silica (Merck "MK 60.9385" [Trade Mark]) eluting with ethyl acetate:methanol, 10:1. Combination and evaporation of the appropriate fractions afforded a solid which on recrystallisation from ethyl acetate/methanol gave 8-methyl-6-(5-bromo-2,4-dimethylimidazol-1-yl)-2-(1H)-quinolone, m.p. 273°, (0.277 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04728653 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-65c727e4d99b429aa4dadae1dbb44ef0 |
| Source note | uspto-grants-1988_03 |