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Ethyl Acetate → 4-[2-chloro-4-({5-[2-(2-hydroxyethoxy)ethyl]-5H-pyrrolo[3,2-d]pyrimidin-4-yl}amino)phenoxy]-N-(2,6-difluorophenyl)piperidine-1-carboxamide hydrochloride

HRID 1787075
Notes
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Reaction equation

HRID 1787075 reaction equation
Cl.Cl.C([O:11][CH2:12][CH2:13][O:14][CH2:15][CH2:16][N:17]1[C:25]2[C:24]([NH:26][C:27]3[CH:32]=[CH:31][C:30]([O:33][CH:34]4[CH2:39][CH2:38][NH:37][CH2:36][CH2:35]4)=[C:29]([Cl:40])[CH:28]=3)=[N:23][CH:22]=[N:21][C:20]=2[CH:19]=[CH:18]1)(=O)C1C=CC=CC=1.C(=O)([O-])[O-].[Na+].[Na+].C(OCC)(=O)C.[F:53][C:54]1[CH:59]=[CH:58][CH:57]=[C:56]([F:60])[C:55]=1[N:61]=[C:62]=[O:63]>O.O1CCCC1>[ClH:40].[Cl:40][C:29]1[CH:28]=[C:27]([NH:26][C:24]2[C:25]3[N:17]([CH2:16][CH2:15][O:14][CH2:13][CH2:12][OH:11])[CH:18]=[CH:19][C:20]=3[N:21]=[CH:22][N:23]=2)[CH:32]=[CH:31][C:30]=1[O:33][CH:34]1[CH2:35][CH2:36][N:37]([C:62]([NH:61][C:55]2[C:56]([F:60])=[CH:57][CH:58]=[CH:59][C:54]=2[F:53])=[O:63])[CH2:38][CH2:39]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 8857Ethyl AcetateHCID 10340Sodium CarbonateHCID 5221622,6-Difluorophenyl isocyanateHCID 675206272-[2-(4-{[3-chloro-4-(piperidin-4-yloxy)phenyl]amino}-5H-pyrrolo[3,2-d]pyrimidin-5-yl)ethoxy]ethyl benzoate dihydrochloride

Product 1

HCID 67521221
4-[2-chloro-4-({5-[2-(2-hydroxyethoxy)ethyl]-5H-pyrrolo[3,2-d]pyrimidin-4-yl}amino)phenoxy]-N-(2,6-difluorophenyl)piperidine-1-carboxamide hydrochloride
Yield 129.4%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8028TetrahydrofuranSolvent

Procedure

To a mixture of 2-[2-(4-{[3-chloro-4-(piperidin-4-yloxy)phenyl]amino}-5H-pyrrolo[3,2-d]pyrimidin-5-yl)ethoxy]ethyl benzoate dihydrochloride (305 mg), 10% aqueous sodium carbonate solution (10 mL), ethyl acetate (15 mL) and tetrahydrofuran (5 mL) was added 2,6-difluorophenyl isocyanate (93 mg) with vigorous stirring. The mixture was stirred at room temperature for 2 hrs, water was added and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was dissolved in methanol (8 mL) and tetrahydrofuran (2 mL). 1N Aqueous sodium hydroxide solution (1 mL) was added, and the mixture was stirred at room temperature for 3 hrs. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The ethyl acetate layer washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was subjected to basic silica gel column chromatography (eluent, methanol:ethyl acetate=0:100→15:85). The object fraction was concentrated under reduced pressure. The residue was dissolved in ethyl acetate-ethanol, and 1N hydrochloric acid/ethyl acetate solution (0.5 mL) was added. The solvent was evaporated under reduced pressure and the obtained residue was crystallized from ethanol-ethyl acetate to give the title compound (202 mg) as a white powder.

Workup

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe ethyl acetate layer was washed with saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customThe solvent was evaporated under reduced pressure
  5. dissolutionthe obtained residue was dissolved in methanol (8 mL)
  6. addition1N Aqueous sodium hydroxide solution (1 mL) was added
  7. stirringthe mixture was stirred at room temperature for 3 hrs
  8. additionWater was added to the reaction mixture
  9. extractionthe mixture was extracted with ethyl acetate
  10. washThe ethyl acetate layer washed with saturated brine
  11. dry with materialdried over anhydrous magnesium sulfate
  12. customThe solvent was evaporated under reduced pressure
  13. concentrationThe object fraction was concentrated under reduced pressure
  14. dissolutionThe residue was dissolved in ethyl acetate-ethanol
  15. addition1N hydrochloric acid/ethyl acetate solution (0.5 mL) was added
  16. customThe solvent was evaporated under reduced pressure
  17. customthe obtained residue was crystallized from ethanol-ethyl acetate

Sources & evidence

ORD record
ord-b5f1f56301ff4b608fed21fa38c80fa3
Source dataset
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07507740B2

Reaction notes

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