HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromo-2,6-dimethylphenol → HCID 69898859, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromo-2,6-dimethylphenol | HCID 16919 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 86584333 | HCID 86584333 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 69898859 | HCID 69898859 | — |
Reaction Conditions
| Temperature | 160 °C |
|---|
Reaction Steps
To a mixture of 2-chloro-4-(1-ethyl-propylamino)-6-methyl-nicotinamide and 2,6-dimethyl-4-bromo-phenol in NMP was added t-BuOK. The resulting mixture was heated in a 160° C. oil bath overnight. The mixture was quenched with water and extracted with ethyl acetate. The organic layer was separated, dried and concentrated, then purified through silica gel Biotage to give the title compound. 1H NMR(CDCl3) d 9.69(d,1H), 7.89(brs,1H), 7.20(s,2H), 6.13(s,1H), 5.5(brs,1H), 3.3(m,1H), 2.10(s,3H), 2.09(s,6H), 1.6(m,4H), 0.95(t,6H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06833378B2 |
| Source dataset | uspto-grants-2004_12 |
| ORD ID | ord-1ab5f1ab35694250aa39855b90cae1b0 |
| Source note | uspto-grants-2004_12 |