Water → HCID 10665616, compound

HRID 1585667Notes

Reaction equation

HRID 1585667 reaction equation
C([O:8][CH2:9][CH2:10][S:11][C:12]([F:30])([F:29])[C:13]([C:21]1[CH:26]=[CH:25][C:24]([F:27])=[CH:23][C:22]=1[F:28])([OH:20])[CH2:14][N:15]1[CH:19]=[N:18][CH:17]=[N:16]1)C1C=CC=CC=1.[H][H].O>C(O)C.[Pd]>[F:28][C:22]1[CH:23]=[C:24]([F:27])[CH:25]=[CH:26][C:21]=1[C:13]([OH:20])([CH2:14][N:15]1[CH:19]=[N:18][CH:17]=[N:16]1)[C:12]([F:30])([F:29])[S:11][CH2:10][CH2:9][OH:8]

Participants

6

Procedure

To a solution of 1-(2-benzyloxyethyl)thio-2-(2,4-difluorophenyl)-1,1-difluoro-3-(1H-1,2,4-triazol-1-yl)propan-2-ol (1.0 g, 2.2 mmol) in ethanol (20 ml), palladium black (20 mg, catalytic) was added, followed by stirring at room temperature and 1 atmospheric pressure in a hydrogen gas for 12 hours. After the completion of the reaction, an insoluble matter was filtered off. The solvent was then distilled off under reduced pressure. To the residue so obtained, water was added, followed by extraction with chloroform. The chloroform solution was washed with water, dried over magnesium sulfate and then distilled off under reduced pressure. To the residue, isopropyl ether was added for crystallization, whereby 2-(2,4-difluorphenyl)-1,1-difluoro-1-(2-hydroxyethyl)thio-3-(1H-1,2,4-triazol-1-yl)propan-2-ol (0.46 g, yield: 55.0%) was obtained as colorless crystals.

Workup

  1. customAfter the completion of the reaction
  2. filtrationan insoluble matter was filtered off
  3. distillationThe solvent was then distilled off under reduced pressure
  4. customTo the residue so obtained
  5. extractionfollowed by extraction with chloroform
  6. washThe chloroform solution was washed with water
  7. dry with materialdried over magnesium sulfate
  8. distillationdistilled off under reduced pressure
  9. additionTo the residue, isopropyl ether was added for crystallization

Sources & evidence

ORD record
ord-bd0a3419d05b41418739deafa1a149dc
Source dataset
uspto-grants-1999_08
Patent number
US05939448

Reaction notes

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