Potassium Hydroxide → HCID 69419669, compound

HRID 1271576Notes

Reaction equation

HRID 1271576 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:12]([NH:14][CH2:15][CH:16]2[CH2:21][CH2:20][N:19](C(OCC)=O)[CH2:18][CH:17]2[O:27][CH3:28])=[O:13])[C:5]2[O:10][CH2:9][CH2:8][O:7][C:6]=2[CH:11]=1.[OH-].[K+]>C(O)C>[Cl:1][C:2]1[CH:3]=[C:4]([C:12]([NH:14][CH2:15][C@H:16]2[CH2:21][CH2:20][NH:19][CH2:18][C@H:17]2[O:27][CH3:28])=[O:13])[C:5]2[O:10][CH2:9][CH2:8][O:7][C:6]=2[CH:11]=1

Participants

4

Reactant 2

HCID 14797Potassium HydroxideHCID 18613663Ethyl 4-[[[(7-chloro-2,3-dihydro-1,4-benzodioxin-5-yl)carbonyl]-amino]methyl]-3-methoxy-1-piperidinecarboxylate

Product 1

HCID 69419669HCID 69419669, compoundYield 51.8%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A mixture of ethyl 4-[[[(7-chloro-2,3-dihydro-1,4-benzodioxin-5-yl)carbonyl]-amino]methyl]-3-methoxy-1-piperidinecarboxylate (0.051 mol) and potassium hydroxide (0.5 mol) in ethanol (200 ml) was stirred and refluxed for 30 hours and then cooled. The solvent was evaporated. The residue was dissolved in water and the solvent was evaporated again. The residue was partitioned between DCM and water. The organic layer was separated, dried, filtered, and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/(CH3OH/NH3)93/7). The pure fractions were collected and the solvent was evaporated, yielding 9 g of (cis)-7-chloro-2,3-dihydro-N-[(3-methoxy-4-piperidinyl)methyl]-1,4-benzodioxin-5-carboxamide (interm. 3-i). Part of interm. (3-i) was dissolved in 2-propanol and converted into the ethanedioic acid salt (1:1). The precipitate was filtered off and dried, yielding 1.2 g of (cis)-7-chloro-2,3-dihydro-N-[(3-methoxy-4-piperidinyl)methyl]-1,4-benzodioxin-5-carboxamide ethanedioate (1:1) (interm. 3-j, mp. 208° C.).

Workup

  1. temperaturerefluxed for 30 hours
  2. temperaturecooled
  3. customThe solvent was evaporated
  4. dissolutionThe residue was dissolved in water
  5. customthe solvent was evaporated again
  6. customThe residue was partitioned between DCM and water
  7. customThe organic layer was separated
  8. customdried
  9. filtrationfiltered
  10. customthe solvent was evaporated
  11. customThe residue was purified by column chromatography over silica gel (eluent: CH2Cl2/(CH3OH/NH3)93/7)
  12. customThe pure fractions were collected
  13. customthe solvent was evaporated

Sources & evidence

ORD record
ord-08748ad46e024297b67031fca5e0e036
Source dataset
uspto-grants-2007_04
Patent number
US07205410B2

Reaction notes

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