HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 11603028, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methanesulfonic acid 2-[2-(4-bromo-phenyl)-5-methyl-oxazol-4-yl]-ethyl ester | HCID 11451238 | — |
| Reactant | HCID 86614640 | HCID 86614640 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11603028 | HCID 11603028 | 62.2% |
Reaction Steps
Prepare using the method of Example 102 with 2-[2-(4-bromophenyl)-5-methyl-1,3-oxazol-4-yl]ethyl methanesulfonate (See Intermediate 13) (0.16 g, 0.44 mmole), anhydrous acetonitrile (2 mL), potassium carbonate (0.21 g, 1.54 mmol), potassium iodide (0.007 g, 0.04 mmol) and (3S)-3-methoxypyrrolidine 4-methylbenzenesulfonate (salt) (See Intermediate 61) (0.22 g, 0.79 mmol) to give the title compound as a pale orange oil (0.10 g): MS (m/e) (79Br/81Br): 371, 373(M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07666871B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-42a0f0631cf24b8da9aa5be73847d766 |
| Source note | uspto-grants-2010_02 |