Pyridine → HCID 89705558, compound
Reaction equation
[C:1]([C@@H:4]1[CH2:8][C:7]([F:10])([F:9])[CH2:6][N:5]1[C:11](=[O:21])[CH2:12][NH:13][C:14](=[O:20])[O:15][C:16]([CH3:19])([CH3:18])[CH3:17])(=O)[NH2:2].N1C=CC=CC=1.FC(F)(F)C(OC(=O)C(F)(F)F)=O>C1COCC1.C(Cl)Cl>[C:1]([C@@H:4]1[CH2:8][C:7]([F:9])([F:10])[CH2:6][N:5]1[C:11](=[O:21])[CH2:12][NH:13][C:14](=[O:20])[O:15][C:16]([CH3:17])([CH3:18])[CH3:19])#[N:2]Participants
Procedure
In a 50 mL round-bottomed flask (S)-tert-butyl 2-(2-carbamoyl-4,4-difluoropyrrolidin-1-yl)-2-oxoethylcarbamate (41) (0.720 g, 2.343 mmol) was dissolved in dry THF at −15° C. Then pyridine was added, followed by the dropwise addition of the solution of 2,2,2-trifluoroacetic anhydride (0.094 ml, 0.664 mmol) in 5 mL of DCM after the complete addition, the mixture was allowed to reach RT. The reaction mixture was stirred for 90 minutes. The reaction mixture was washed with 1M solution of aqueous solution of hydrochloric acid. Then the organic layer was washed three times with saturated sodium bicarbonate, brine, dried over sodium sulfate and evaporated. The crude mixture was purified using column chromatography (hexane-ethyl acetate 2-3) yielding a yellowish oil Yield: 0.678 g, 70%
Workup
- additionafter the complete addition
- customto reach RT
- washThe reaction mixture was washed with 1M solution of aqueous solution of hydrochloric acid
- washThen the organic layer was washed three times with saturated sodium bicarbonate, brine
- dry with materialdried over sodium sulfate
- customevaporated
- customThe crude mixture was purified
Sources & evidence
- ORD record
- ord-98c54cf1ec564ab4b611ee8cc41a23ea
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09346814B2
Reaction notes
Loading…