HCID 68595080, compound → HCID 68595970, compound
Reaction equation
[F:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[O:10][C:9]([CH2:13][F:14])([CH3:12])[CH2:8][C@H:7]2[NH2:15].[Li]CCCC>C1COCC1>[F:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[O:10][C@@:9]([CH2:13][F:14])([CH3:12])[CH2:8][C@H:7]2[NH2:15]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of Example 128A (1.99 g, 9.34 mmol) in THF (100 mL) was cooled to 0° C. and n-BuLi (3.74 mL of a 2.5M solution in hexanes, 9.34 mmol) was added while maintaining the internal temperature <0° C. The reaction was warmed to ambient temperature and n-BuLi was added twice more (2 mL for each addition). After 30 minutes, the reaction was quenched by addition of water (25 mL) and extracted with MTBE (50 mL). The organic portion was washed with brine (25 mL), dried (Na2SO4), filtered, and concentrated. The residue was purified by silica gel chromatography (gradient elution: 0-10% MeOH/EtOAc) to give the title compound (490 mg, 2.30 mmol, 25% yield). MS (LCMS) m/z 197 (M−NH2)+.
Workup
- temperaturewhile maintaining the internal temperature <0° C
- additionfor each addition)
- customthe reaction was quenched by addition of water (25 mL)
- extractionextracted with MTBE (50 mL)
- washThe organic portion was washed with brine (25 mL)
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated
- customThe residue was purified by silica gel chromatography (gradient elution: 0-10% MeOH/EtOAc)
Sources & evidence
- ORD record
- ord-fe095e41f37c4b1383f899d9fdf3e8f3
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08609692B2
Reaction notes
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