Acetic Acid → HCID 68138826, compound

HRID 1578692Notes

Reaction equation

HRID 1578692 reaction equation
[CH3:1][N:2]1[CH2:7][CH2:6][C:5](=O)[CH2:4][CH2:3]1.C(O)(=O)C.[NH2:13][C:14]1[CH:19]=[C:18]([Cl:20])[CH:17]=[CH:16][C:15]=1[N:21]1[CH:25]=[CH:24][CH:23]=[CH:22]1>C(O)C>[ClH:20].[Cl:20][C:18]1[CH:19]=[C:14]2[C:15](=[CH:16][CH:17]=1)[N:21]1[CH:22]=[CH:23][CH:24]=[C:25]1[C:5]1([CH2:6][CH2:7][N:2]([CH3:1])[CH2:3][CH2:4]1)[NH:13]2

Participants

5

Procedure

1.7 g (0.016 mole) of 1-methyl-4-piperidone and 3 ml. of glacial acetic acid are added to a solution of 2.7 g (0.014 mole) of 1-(2-amino-4-chloro-phenyl) pyrrole, Example 13(b), in 50 ml. of absolute ethanol. The solution is refluxed for 36 hours and concentrated, and the residue dissolved in water. The aqueous solution is filtered, and the filtrate is basified. A solid precipitates, is filtered, and dried. The solid is dissolved in ether and ethereal-hydrogen chloride is added. The resulting precipitate is filtered, dried, and recrystallized from methanol to give 7-chloro-4,5-dihydro-1'-methylspiro-[pyrrolo (1,2-a)quinoxaline-4,4'-piperidine] hydrochloride, m.p. 297°-298° C.

Workup

  1. temperatureThe solution is refluxed for 36 hours
  2. concentrationconcentrated
  3. dissolutionthe residue dissolved in water
  4. filtrationThe aqueous solution is filtered
  5. customA solid precipitates
  6. filtrationis filtered
  7. customdried
  8. dissolutionThe solid is dissolved in ether
  9. additionethereal-hydrogen chloride is added
  10. filtrationThe resulting precipitate is filtered
  11. customdried
  12. customrecrystallized from methanol

Sources & evidence

ORD record
ord-7028a80601274b37b4bdf27c413e94b1
Source dataset
uspto-grants-1976_02
Patent number
US03939159

Reaction notes

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