Dichloromethane → HCID 57482543, compound

HRID 1916204Notes

Reaction equation

HRID 1916204 reaction equation
[S:1]1[CH:5]=[CH:4][C:3]2[C:6]([N:10]3[CH2:15][CH2:14][N:13](C(OC(C)(C)C)=O)[CH2:12][CH:11]3[CH3:23])=[CH:7][CH:8]=[CH:9][C:2]1=2.FC(F)(F)C(O)=O.C(Cl)[Cl:32]>>[ClH:32].[ClH:32].[S:1]1[CH:5]=[CH:4][C:3]2[C:6]([N:10]3[CH2:15][CH2:14][NH:13][CH2:12][CH:11]3[CH3:23])=[CH:7][CH:8]=[CH:9][C:2]1=2

Participants

4

Procedure

A solution of 1.22 g (3.7 mmol) of tert-butyl 4-benzo[b]thiophen-4-yl-3-methylpiperazin-1-carboxylate in methylene chloride (12 ml) was added to trifluoroacetic acid (6 ml), and the mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure, then an aqueous solution of 5% potassium carbonate was added to the residue and the resulting mixture was extracted with methylene chloride. The organic phase was dried over magnesium sulfate and concentrated under reduced pressure. Concentrated hydrochloric acid (6 ml) and methanol (10 ml) were added to the residue and the resulting mixture was concentrated under reduced pressure. The residue was recrystallized from acetonitrile to obtain 1-benzo[b]thiophen-4-yl-2-methylpiperazine dihydrochloride (0.98 g) as light brown powder.

Workup

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. additionan aqueous solution of 5% potassium carbonate was added to the residue
  3. extractionthe resulting mixture was extracted with methylene chloride
  4. dry with materialThe organic phase was dried over magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. additionConcentrated hydrochloric acid (6 ml) and methanol (10 ml) were added to the residue
  7. concentrationthe resulting mixture was concentrated under reduced pressure
  8. customThe residue was recrystallized from acetonitrile

Sources & evidence

ORD record
ord-80db4919369042a8a7d9d117921013a3
Source dataset
uspto-grants-2013_12
Patent number
US08618109B2

Reaction notes

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