HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfide → 3-(4-Trifluoromethoxy-phenyl)-3,9-diaza-bicyclo[3.3.1]nonane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Pyridine, 1,2,3,6-tetrahydro-4-[4-(trifluoromethyl)phenyl]- | HCID 12440708 | — |
| Reactant | 3-(4-Trifluoromethoxyphenyl)-3,9-diaza-bicyclo[3.3.1]nonane-2,4-dione | HCID 67045999 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Trifluoromethoxy-phenyl)-3,9-diaza-bicyclo[3.3.1]nonane | HCID 67046014 | — |
Reaction Steps
A solution of 3-(4-trifluoromethoxy-phenyl)-3,9-diaza-bicyclo[3.3.1]nonane-2,4-dione (80 mg, 0.25 mmol) and THF (4 mL) was heated at 70° C. under N2. A solution of BH3.SMe2 (2M in THF, 0.4 mL, 0.8 mmol) was added dropwise. After 40 min, 6N HCl (1.0 mL) was added dropwise (Caution: H2 evolution). After an additional 30 min, the reaction was poured into 1N NaOH (8 mL) and extracted with dichloromethane (30 mL×2). The combined organic extracts were dried, filtered and concentrated to give 3-(4-trifluoromethoxy-phenyl)-3,9-diaza-bicyclo[3.3.1]nonane: MS (ESI): 287.5 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915253B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-4f467add4c6e492aa220af051098d209 |
| Source note | uspto-grants-2011_03 |