Acetonitrile → HCID 86754613, compound

HRID 611845Notes

Reaction equation

HRID 611845 reaction equation
[F:1][C:2]1[CH:16]=[CH:15][C:5]2[C:6]([CH:9]3[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]3)=[N:7][O:8][C:4]=2[CH:3]=1.C1(S(O[CH2:27][CH2:28][CH2:29][O:30][C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=2NC(=O)C)(=O)=O)C=CC=CC=1.C([O-])([O-])=[O:42].[K+].[K+].[C:47](#[N:49])[CH3:48]>O>[F:1][C:2]1[CH:16]=[CH:15][C:5]2[C:6]([CH:9]3[CH2:10][CH2:11][N:12]([CH2:27][CH2:28][CH2:29][O:30][C:31]4[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=4[CH2:48][C:47]([NH2:49])=[O:42])[CH2:13][CH2:14]3)=[N:7][O:8][C:4]=2[CH:3]=1

Participants

6

Reactant 4

HCID 6342AcetonitrileHCID 11430Potassium CarbonateHCID 8494213-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 21960096N-[2-(3-phenylsulfonyloxypropoxy)phenyl]acetamide

Product 1

HCID 86754613HCID 86754613, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (3.4 g, 16 mmol), N-[2-(3-phenylsulfonyloxypropoxy)phenyl]acetamide (5.3 g, 16 mmol), K2CO3 (2.2 g), and acetonitrile (50 ml) was stirred and refluxed for 5 hours. The reaction was poured into water, and the aqueous suspension was extracted with ethyl acetate. The ethyl acetate was washed (water and brine), dried (MgSO4) and the solvent was concentrated to afford 6.0 g of a thick, brown oil. The oil was chromatographed on a Waters Prep 500 LC on silica gel. Concentration of the appropriate fractions afforded 3.0 g of a beige solid. This was recrystallized from ethyl acetate to yield (with concentration of the mother liquors) 2.2 g (33%) of N-[2-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]phenyl]acetamide as a beige solid, m.p.=118-120° C.

Workup

  1. temperaturerefluxed for 5 hours
  2. extractionthe aqueous suspension was extracted with ethyl acetate
  3. washThe ethyl acetate was washed (water and brine)
  4. dry with materialdried (MgSO4)
  5. concentrationthe solvent was concentrated
  6. customto afford 6.0 g of a thick, brown oil
  7. customThe oil was chromatographed on a Waters Prep 500 LC on silica gel

Sources & evidence

ORD record
ord-c187f334c9194fecbfc24c47f436feda
Source dataset
uspto-grants-1999_12
Patent number
US06001834

Reaction notes

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