Hydrochloric Acid → HCID 19086843, compound

HRID 1464620Notes

Reaction equation

HRID 1464620 reaction equation
C1CO[C:3]2([CH2:8][CH2:7][N:6]([C:9]([C:11]3[CH:12]=[C:13]4[C:18](=[CH:19][CH:20]=3)[NH:17][C:16](=[O:21])[CH2:15][CH2:14]4)=[O:10])[CH2:5][CH2:4]2)[O:2]1.Cl.C(=O)([O-])[O-].[Na+].[Na+].ClCCl>O1CCOCC1.O.CO>[O:2]=[C:3]1[CH2:8][CH2:7][N:6]([C:9]([C:11]2[CH:12]=[C:13]3[C:18](=[CH:19][CH:20]=2)[NH:17][C:16](=[O:21])[CH2:15][CH2:14]3)=[O:10])[CH2:5][CH2:4]1

Participants

8

Conditions

Temperature
100 °C

Procedure

46 Grams of 6-(4,4-ethylenedioxy-1-piperidylcarbonyl)3,4-dihydrocarbostyril was dispersed in 400 ml of dioxane and 150 ml of water, then 15 ml of concentrated hydrochloric acid was added thereto and the whole mixture was heated at 100° C. for 7 hours with stirring. After the reaction mixture was allowed to stand for cooling, then was made alkaline by adding sodium carbonate, and the solvent was removed by evaporation. The residue thus obtained was extracted with chloroform, and the extract was dried with anhydrous sodium carbonate, and the solvent was removed by evaporation. The residue thus obtained was purlfied by means of a silica gel column chromatography (eluent:dichloromethane:methanol=10:1) to yield 37.6 g of 6-(4-oxo-1-piperidylcarbonyl)-3,4-dihydrocarbostyril.

Workup

  1. temperaturefor cooling
  2. customthe solvent was removed by evaporation
  3. customThe residue thus obtained
  4. extractionwas extracted with chloroform
  5. dry with materialthe extract was dried with anhydrous sodium carbonate
  6. customthe solvent was removed by evaporation
  7. customThe residue thus obtained

Sources & evidence

ORD record
ord-f57ba2fa5f184ca495d086d93d901ca5
Source dataset
uspto-grants-1994_04
Patent number
US05306719

Reaction notes

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