HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-methoxy-N-methyl-6-(trifluoromethyl)nicotinamide → HCID 86716070, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-methoxy-N-methyl-6-(trifluoromethyl)nicotinamide | HCID 23116945 | — |
| Reactant | HCID 178478127 | HCID 178478127 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86716070 | HCID 86716070 | — |
Reaction Steps
To a solution of N-methoxy-N-methyl-6-(trifluoromethyl)nicotinamide (1.23 g, 5.25 mmol, Intermediate 15, step b) in THF (12 mL) at 4° C. was added 0.5 M (3-chlorophenyl)magnesium bromide in THF (12.7 mL, 6.35 mmol). The mixture was stirred at 4° C. to room temperature overnight, and quenched with NH4Cl (aqueous). The organic layer was separated, and the aqueous layer was extracted with CH2Cl2. The combined organic phases were dried (Na2SO4), filtered, concentrated, and purified by flash column chromatography (40 g silica gel column, 0-70% EtOAc in heptanes) to give the title compound as an oil, which solidified upon standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09309222B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-15c642f432974fbc94f6c25f9409480d |
| Source note | uspto-grants-2016_04 |