HCID 68595080, compound → HCID 68595970, compound

HRID 1913312Notes

Reaction equation

HRID 1913312 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

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

  1. temperaturewhile maintaining the internal temperature <0° C
  2. additionfor each addition)
  3. customthe reaction was quenched by addition of water (25 mL)
  4. extractionextracted with MTBE (50 mL)
  5. washThe organic portion was washed with brine (25 mL)
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated
  9. 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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