HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-(3,5-Bis-trifluoromethyl-phenyl)-N-(6'-chloro-2-methyl-[3,4]bipyridinyl-3'-yl)-N-methyl-isobutyramide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(3,5-Bis(trifluoromethyl)phenyl)-2-methylpropanoyl chloride | HCID 11267141 | — |
| Reactant | 6'-Chloro-N,2-dimethyl-[3,4'-bipyridin]-3'-amine | HCID 58694606 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3,5-Bis-trifluoromethyl-phenyl)-N-(6'-chloro-2-methyl-[3,4]bipyridinyl-3'-yl)-N-methyl-isobutyramide | HCID 21083635 | — |
Reaction Steps
To a solution of (6′-chloro-2-methyl-[3,4′]bipyridinyl-3′-yl)-methyl-amine in THF is added a solution of n-butyllithium in hexanes at about −78° C. After 15 min 2-(3,5-bis-trifluoromethyl-phenyl)-2-methyl-propionyl chloride is added. The reaction mixture is allowed to warm to room temperature during 30 min. After addition of an aqueous sodium hydroxide solution, the mixture is extracted with dichloromethane, dried and concentrated to give the compound 2-(3,5-Bis-trifluoromethyl-phenyl)-N-(6′-chloro-2-methyl-[3,4′]bipyridinyl-3′-yl)-N-methyl-isobutyramide of formula II-2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07176205B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-ea8fb2a6a11d4830890dea7a9e4484f6 |
| Source note | uspto-grants-2007_02 |