Sodium Carbonate → HCID 25004350, compound

HRID 2401682Notes

Reaction equation

HRID 2401682 reaction equation
[O:1]1[CH2:6][CH2:5][CH:4]([NH:7][C:8]2[CH:13]=[CH:12][C:11](B3OC(C)(C)C(C)(C)O3)=[CH:10][C:9]=2[C:23]([F:26])([F:25])[F:24])[CH2:3][CH2:2]1.C([O-])([O-])=O.[Na+].[Na+].Br[C:34]1[CH:39]=[CH:38][N:37]([CH2:40][CH:41]2[CH2:43][CH2:42]2)[C:36](=[O:44])[C:35]=1[C:45]#[N:46]>O1CCOCC1.CCOC(C)=O.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:41]1([CH2:40][N:37]2[CH:38]=[CH:39][C:34]([C:11]3[CH:12]=[CH:13][C:8]([NH:7][CH:4]4[CH2:3][CH2:2][O:1][CH2:6][CH2:5]4)=[C:9]([C:23]([F:24])([F:25])[F:26])[CH:10]=3)=[C:35]([C:45]#[N:46])[C:36]2=[O:44])[CH2:42][CH2:43]1

Participants

7

Reactant 3

HCID 10340Sodium CarbonateHCID 59234229HCID 59234229, compoundHCID 59272913HCID 59272913, compound

Product 1

HCID 25004350HCID 25004350, compoundYield 83.6%

Reagents, catalysts & solvents 3

HCID 178418397HCID 178418397, compoundCatalystHCID 8857Ethyl AcetateSolventHCID 312751,4-DioxaneSolvent

Procedure

To a solution of intermediate 17 (0.63 g, 1.69 mmol) in 1,4-dioxane (3 ml) and a saturated solution of Na2CO3 (3 ml) was added intermediate 8 (0.42 g, 1.69 mmol). The resulting solution was degassed using a stream of nitrogen and to this was added Pd(PPh3)4 (0.19 mg, 0.17 mmol). The reaction was then microwaved in a sealed tube at 150° C. for 10 minutes. The resulting cooled reaction mixture was then diluted with EtOAc and filtered through a pad of diatomaceous earth. The filtrate was washed with brine, dried over Na2SO4 and concentrated in vacuo. The crude reaction mixture was then purified by column chromatography (silica gel; DCM to DCM/EtOAc up to 30% as eluent). The desired fractions were collected and evaporated in vacuo to yield compound 3 (0.59 g, 9%).

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. filtrationfiltered through a pad of diatomaceous earth
  6. washThe filtrate was washed with brine
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated in vacuo
  9. customThe crude reaction mixture
  10. customwas then purified by column chromatography (silica gel; DCM to DCM/EtOAc up to 30% as eluent)
  11. customThe desired fractions were collected
  12. customevaporated in vacuo

Sources & evidence

ORD record
ord-8e9643319623494182cb92994a08f22f
Source dataset
uspto-grants-2014_08
Patent number
US08796311B2

Reaction notes

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