Potassium Carbonate → HCID 86749837, compound

HRID 743521Notes

Reaction equation

HRID 743521 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.[C:17]([O-:20])([O-])=O.[K+].[K+].BrCCCO[C:28]1[CH:33]=[CH:32][C:31]([C:34]2(C=O)[CH:39]=[CH:38][CH:37]=[CH:36][CH2:35]2)=[CH:30][C:29]=1[O:42][CH3:43]>C(#N)C>[F:1][C:2]1[CH:16]=[CH:15][C:5]2[C:6]([CH:9]3[CH2:10][CH2:11][N:12]([CH2:2][CH2:3][CH2:4][O:8][C:30]4[C:29]([O:42][CH3:43])=[CH:28][CH:33]=[CH:32][C:31]=4[C:34]4[CH:35]=[CH:36][C:37]([CH:17]=[O:20])=[CH:38][CH:39]=4)[CH2:13][CH2:14]3)=[N:7][O:8][C:4]=2[CH:3]=1

Participants

5

Reactant 3

HCID 11430Potassium CarbonateHCID 8494213-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 867482531-[4-(3-Bromopropoxy)-3-methoxyphenyl] phenylmethanone

Product 1

HCID 86749837HCID 86749837, compoundYield 173.6%

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (2.2 g, 10 mmol), K2CO3 (2.3 g) and 1-[4-(3-bromopropoxy)-3-methoxyphenyl]phenylmethanone (3.47 g, 10 mmol) in acetonitrile (100 ml) was heated at reflux for 3 hours. At the end of reaction, the acetonitrile was concentrated and the mixture was extracted into dichloromethane (200 ml). The insolubles were filtered off and the solvent was evaporated to an oil. Purification was carried out by flash chromatography over a silica gel column (SiO2, 50 g; eluted with dichloromethane, 600 ml; 1% methanol:dichloromethane, 600 ml; 2% methanol: 98% dichloromethane, 600 ml). The fractions containing the pure product were combined and concentrated to give 4.24 g (87%) of an off-white solid. Recrystallization from ethanol (75 ml) gave 3.9 g of 1-[4-[3-[4-(6-fluoro-1,2-benziosoxazol-3- yl)- 1-piperidinyl]-propoxy]-3-methoxyphenyl]phenylmethanone as off-white crystals, m.p.=128°-130° C.

Workup

  1. temperaturewas heated
  2. temperatureat reflux for 3 hours
  3. customAt the end of reaction
  4. concentrationthe acetonitrile was concentrated
  5. extractionthe mixture was extracted into dichloromethane (200 ml)
  6. filtrationThe insolubles were filtered off
  7. customthe solvent was evaporated to an oil
  8. customPurification
  9. washwas carried out by flash chromatography over a silica gel column (SiO2, 50 g; eluted with dichloromethane, 600 ml; 1% methanol:dichloromethane, 600 ml; 2% methanol: 98% dichloromethane, 600 ml)
  10. additionThe fractions containing the pure product
  11. concentrationconcentrated

Sources & evidence

ORD record
ord-0d4e2baf0b8040778a9f5549a155c0a6
Source dataset
uspto-grants-1996_09
Patent number
US05556858

Reaction notes

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