Sodium borohydride → 2-(5-amino-3-phenyl-4-(phenylethynyl)-1H-pyrazol-1-yl)ethan-1-ol

HRID 588622Notes

Reaction equation

HRID 588622 reaction equation
C([NH:4][C:5]1[N:9]([CH2:10][C:11](OCC)=[O:12])[N:8]=[C:7]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[C:6]=1[C:22]#[C:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)(=O)C.[BH4-].[Na+]>C(O)C>[NH2:4][C:5]1[N:9]([CH2:10][CH2:11][OH:12])[N:8]=[C:7]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[C:6]=1[C:22]#[C:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1

Participants

4

Procedure

To a suspension of ethyl 2-[5-acetamido-3-phenyl-4-(2-phenylethynyl)pyrazol-1-yl]acetate (22.4 g, 58 mmol) in ethanol (290 mL) was added sodium borohydride (11 g, 289 mmol) and the reaction stirred at room temperature for 16 h. The reaction mixture was partially concentrated to a final volume of 250 mL. 25% NaOH (250 mL) was added and the reaction mixture was stirred at 80° C. for 4 h. The reaction mixture was cooled down to room temperature and the two phases were separated. The aqueous phase was extracted with ethyl acetate three times and the organic phases combined, dried over MgSO4, filtered and evaporated. The residue was triturated from diethyl ether (20 mL) and the product was filtered and dried in vacuo to provide the title compound as an off-white solid (9.96 g). The mother liquor was concentrated in vacuo and purified by column chromatography (silica gel, gradient 0 to 100% ethyl acetate/isohexane) yielding a further 1.79 g of the title compound.

Workup

  1. concentrationThe reaction mixture was partially concentrated to a final volume of 250 mL
  2. addition25% NaOH (250 mL) was added
  3. stirringthe reaction mixture was stirred at 80° C. for 4 h
  4. temperatureThe reaction mixture was cooled down to room temperature
  5. customthe two phases were separated
  6. extractionThe aqueous phase was extracted with ethyl acetate three times
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. customevaporated
  10. customThe residue was triturated from diethyl ether (20 mL)
  11. filtrationthe product was filtered
  12. customdried in vacuo

Sources & evidence

ORD record
ord-ff0b4af643514bd492c5cb2d21083bbe
Source dataset
uspto-grants-2016_01
Patent number
US09227976B2

Reaction notes

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