Cesium carbonate → (E)-4-(2-(2,4-Dichlorophenyl)-1-(1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl)but-1-en-1-yl)benzaldehyde

HRID 2069591Notes

Reaction equation

HRID 2069591 reaction equation
[C:1]([C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[N:10]([CH:14]1[CH2:19][CH2:18][CH2:17][CH2:16][O:15]1)[N:9]=[CH:8]2)#[C:2][CH2:3][CH3:4].B1(B2OC(C)(C)C(C)(C)O2)OC(C)(C)C(C)(C)O1.I[C:39]1[CH:46]=[CH:45][C:42]([CH:43]=[O:44])=[CH:41][CH:40]=1.C(=O)([O-])[O-].[Cs+].[Cs+].[Cl:53][C:54]1[CH:59]=[C:58]([Cl:60])[CH:57]=[CH:56][C:55]=1I.[OH-].[K+]>C1C=CC([P]([Pt]([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.O1CCOCC1>[Cl:53][C:54]1[CH:59]=[C:58]([Cl:60])[CH:57]=[CH:56][C:55]=1/[C:2](/[CH2:3][CH3:4])=[C:1](\[C:39]1[CH:46]=[CH:45][C:42]([CH:43]=[O:44])=[CH:41][CH:40]=1)/[C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[N:10]([CH:14]1[CH2:19][CH2:18][CH2:17][CH2:16][O:15]1)[N:9]=[CH:8]2

Participants

9

Reactant 6

HCID 10796Cesium carbonateHCID 14797Potassium HydroxideHCID 966574-IodobenzaldehydeHCID 968642,4-Dichloro-1-iodobenzeneHCID 2733548Bis(pinacolato)diboraneHCID 667932705-(But-1-yn-1-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole2×

Product 1

HCID 86663371(E)-4-(2-(2,4-Dichlorophenyl)-1-(1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl)but-1-en-1-yl)benzaldehydeYield 68.5%

Reagents, catalysts & solvents 2

HCID 178420539HCID 178420539, compoundCatalystHCID 312751,4-DioxaneSolvent2×

Procedure

A round-bottom flask equipped with a magnetic stir bar, a reflux condenser, and a N2 inlet was charged with 5-(but-1-yn-1-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (20.0 g, 78.6 mmol; Intermediate 3), bis(pinacolato)diboron (20.17 g, 79.4 mmol), tetrakis(triphenylphosphine)platinum (0) (0.98 g, 0.8 mmol), and anhydrous 1,4-dioxane (160 mL). This mixture was degassed with three vacuum/N2 cycles and refluxed for 4 h. The solution was then allowed to cool to room temperature, and 4-iodobenzaldehyde (18.25 g, 78.6 mmol), trans-dichloro(triphenylphosphine)palladium (II) (5.52 g, 7.9 mmol), cesium carbonate (51.24 g, 157.3 mmol), and 1,4-dioxane (160 mL) were added. This mixture was degassed with three vacuum/N2 cycles, and then water (4.7 mL) was added. This mixture was stirred at room temperature for 6 h. 2,4-Dichloroiodobenzene (12.8 mL, 94.4 mmol) and 6M aqueous KOH (62.9 mL) were added, and the mixture was degassed with three vacuum/N2 cycles and refluxed for 4 h. Upon completion, the reaction mixture was filtered through a Celite/silica pad and washed with EtOAc. The filtrate was washed with water (600 mL), washed with brine (300 mL), dried over sodium sulfate, filtered, and concentrated. The crude product was purified by silica gel chromatography (0-20% ethyl acetate in hexanes) to give the title compound (27.2 g, 7:1 mixture of regioisomers) as a yellow foam. Data for major regioisomer: 1H NMR (400 MHz, DMSO-d6): δ 9.83 (s, 1H), 8.16 (s, 1H), 7.77 (d, 1H), 7.73 (s, 1H), 7.65 (d, 2H), 7.53 (d, 1H), 7.41-7.36 (m, 2H), 7.31-7.28 (m, 1H), 7.17 (d, 2H), 5.86 (dd, 1H), 3.92-3.86 (m, 1H), 3.78-3.71 (m, 1H), 2.47-2.38 (m, 3H), 2.10-1.96 (m, 2H), 1.81-1.71 (m, 1H), 1.64-1.58 (m, 2H), 0.94 (t, 3H); LCMS: 421 [(M-THP+H)+H]+.

Workup

  1. customA round-bottom flask equipped with a magnetic stir bar, a reflux condenser, and a N2 inlet
  2. customThis mixture was degassed with three vacuum/N2 cycles
  3. temperaturerefluxed for 4 h
  4. customThis mixture was degassed with three vacuum/N2 cycles
  5. additionwater (4.7 mL) was added
  6. customthe mixture was degassed with three vacuum/N2 cycles
  7. temperaturerefluxed for 4 h
  8. filtrationUpon completion, the reaction mixture was filtered through a Celite/silica pad
  9. washwashed with EtOAc
  10. washThe filtrate was washed with water (600 mL)
  11. washwashed with brine (300 mL)
  12. dry with materialdried over sodium sulfate
  13. filtrationfiltered
  14. concentrationconcentrated
  15. customThe crude product was purified by silica gel chromatography (0-20% ethyl acetate in hexanes)

Sources & evidence

ORD record
ord-fc1575a1e4d3469caf3a13fb9bdbd4cd
Source dataset
uspto-grants-2012_10
Patent number
US08299112B2

Reaction notes

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