Sodium Bicarbonate → HCID 25003297, compound

HRID 2176862Notes

Reaction equation

HRID 2176862 reaction equation
[F:1][C:2]1[CH:16]=[C:15](B2OC(C)(C)C(C)(C)O2)[CH:14]=[CH:13][C:3]=1[O:4][C:5]1[CH:10]=[CH:9][N:8]=[C:7]([CH3:11])[C:6]=1[CH3:12].C([O-])(O)=O.[Na+].Br[C:32]1[CH:37]=[CH:36][N:35]([CH2:38][CH:39]2[CH2:41][CH2:40]2)[C:34](=[O:42])[C:33]=1[C:43]#[N:44]>O1CCOCC1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH:39]1([CH2:38][N:35]2[CH:36]=[CH:37][C:32]([C:15]3[CH:14]=[CH:13][C:3]([O:4][C:5]4[CH:10]=[CH:9][N:8]=[C:7]([CH3:11])[C:6]=4[CH3:12])=[C:2]([F:1])[CH:16]=3)=[C:33]([C:43]#[N:44])[C:34]2=[O:42])[CH2:40][CH2:41]1

Participants

6

Procedure

To a solution of intermediate 24 (1.769 mmol) in 1,4-dioxane (7 ml) and a saturated solution of NaHCO3 (7 ml) was added intermediate 5 (0.38 g, 1.504 mmol). The resulting solution was degassed using a stream of nitrogen and to this was added Pd(PPh3)4 (0.2 mg, 0.176 mmol). The reaction was then microwaved in a sealed tube at 150° C. for 10 minutes. The resulting cooled reaction mixture was filtered through a pad of diatomaceous earth. The filtrate was diluted with EtOAc, and then it was washed with water, dried (Na2SO4) and concentrated in vacuo. The crude reaction mixture was then purified by column chromatography (silica gel; DCM to DCM/MeOH up to 5% as eluent). The desired fractions were collected and evaporated in vacuo to yield compound 11 precipitated from diisopropylether (0.190 g, 32%).

Workup

  1. customThe resulting solution was degassed
  2. customThe reaction was then microwaved in a sealed tube at 150° C. for 10 minutes
  3. temperatureThe resulting cooled
  4. customreaction mixture
  5. filtrationwas filtered through a pad of diatomaceous earth
  6. additionThe filtrate was diluted with EtOAc
  7. washit was washed with water
  8. dry with materialdried (Na2SO4)
  9. concentrationconcentrated in vacuo
  10. customThe crude reaction mixture
  11. customwas then purified by column chromatography (silica gel; DCM to DCM/MeOH up to 5% as eluent)
  12. customThe desired fractions were collected
  13. customevaporated in vacuo

Sources & evidence

ORD record
ord-26d394bc9e154377b2b8cd5868368629
Source dataset
uspto-grants-2015_06
Patent number
US09067891B2

Reaction notes

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