Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | HCID 82374291 | HCID 82374291 | — |
| Reactant | HCID 178419651 | HCID 178419651 | — |
| Catalyst | HCID 178419074 | HCID 178419074 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66777829 | HCID 66777829 | 85% |
Reaction Steps
To a solution (60 mL) of 3-methylthieno[2,3-b]pyridine-2-carbaldehyde (2.07 g) synthesized above in tetrahydrofuran was added a 1.0M solution (17.6 mL) of cyclohexylmagnesium bromide in tetrahydrofuran at 0° C., and the mixture was stirred for 1 hr. Saturated aqueous ammonium chloride solution was added to quench the reaction, and the reaction mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (10-50% ethyl acetate/hexane) to give a yellow solid. To a mixture of the obtained solid, 4-methylmorpholine N-oxide (1.81 g) and acetonitrile (40 mL) was added tetrapropylammonium perruthenate (238 mg), and the mixture was stirred at room temperature for 3 hr, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (0-30% ethyl acetate/hexane) to give the title object compound (1.50 g, 85%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08436043B2 |
|---|
| Source dataset | uspto-grants-2013_05 |
|---|
| ORD ID | ord-d28ca41f5eff4e97aeb2cecf3550d2f2 |
|---|
| Source note | uspto-grants-2013_05 |
|---|