HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 59320816, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 2,4-Dibromo-1,5-dimethyl-1H-imidazole | HCID 7204873 | — |
| Reactant | 1036990-53-0 | HCID 30032997 | — |
| Reactant | HCID 59320805 | HCID 59320805 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | HCID 59320816 | HCID 59320816 | — |
Reaction Steps
4-Bromo-1,2,5-trimethyl-1H-imidazole may be prepared from 2,4-dibromo-1,5-dimethyl-1H-imidazole by treatment with n-butyl lithium and methyl iodide as described in J. Org. Chem., 1994, 59, 5524. This may be coupled with 1-[3-(7-boronic acid-imidazo[1,2-a]pyridin-3-yl)-phenyl]-3-(2,2,2-trifluoro-ethyl)-urea or 1-{3-[7-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-imidazo[1,2-a]pyridin-3-yl]-phenyl}-3-(2,2,2-trifluoro-ethyl)-urea according to procedure E3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895745B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-015b6e61ce1a45b6a3f2a9eb39f45ffd |
| Source note | uspto-grants-2014_11 |