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Benzyl Alcohol → tert-Butyl [3-(6-amino-1-oxo-3,4-dihydroisoquinolin-2(1H)-yl)propyl]methylcarbamate

HRID 446553
Notes
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Reaction equation

HRID 446553 reaction equation
[C:1]([O:5][C:6]([N:8]([CH3:27])[CH2:9][CH2:10][CH2:11][N:12]1[CH2:21][CH2:20][C:19]2[C:14](=[CH:15][CH:16]=[C:17](C(OC)=O)[CH:18]=2)[C:13]1=[O:26])=[O:7])([CH3:4])([CH3:3])[CH3:2].[OH-].[Na+].Cl.[N-:31]=[N+]=[N-].P([O-])(OC1C=CC=CC=1)(OC1C=CC=CC=1)=O.C(N(CC)CC)C.C(O)C1C=CC=CC=1>O1CCCC1.CO.C(OCC)(=O)C>[NH2:31][C:17]1[CH:18]=[C:19]2[C:14](=[CH:15][CH:16]=1)[C:13](=[O:26])[N:12]([CH2:11][CH2:10][CH2:9][N:8]([CH3:27])[C:6](=[O:7])[O:5][C:1]([CH3:4])([CH3:3])[CH3:2])[CH2:21][CH2:20]2
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

10

Reactant 6

HCID 244Benzyl AlcoholHCID 313Hydrochloric AcidHCID 8471TriethylamineHCID 14798Sodium HydroxideHCID 21964642Diphenylphosphate azideHCID 66671432Methyl 2-{3-([tert-butoxycarbonyl)(methyl)amino]propyl}-1-oxo-1,2,3,4-tetrahydroisoquinoline-6-carboxylate

Product 1

HCID 86663453tert-Butyl [3-(6-amino-1-oxo-3,4-dihydroisoquinolin-2(1H)-yl)propyl]methylcarbamateYield 81%

Reagents, catalysts & solvents 3

HCID 887MethanolSolventHCID 8028TetrahydrofuranSolventHCID 8857Ethyl AcetateSolvent

Conditions

Temperature
60 °C

Procedure

The compound (535 mg, 1.41 mmol) obtained in Example 61c was dissolved in a mixed solvent (6 mL) of tetrahydrofuran and methanol (1:1), a 1 N aqueous sodium hydroxide solution (1 mL) was added, and the mixture was stirred at 60° C. for 5 hours. After the reaction was completed, a 1 N aqueous hydrochloric acid solution (10 mL) was added to the reaction mixture under ice cooling, and ethyl acetate was further added to separate the layers. The resulting organic layer was separated, washed with saturated sodium chloride solution, and then dried with anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was dissolved in 1,4-dioxane (6 mL), diphenyl phosphate azide (0.238 mL, 1.10 mmol), triethylamine (0.154 mL, 1.10 mmol) and benzyl alcohol (0.228 mL, 2.21 mmol) were added under ice cooling, and the mixture was stirred at 100° C. under a nitrogen atmosphere for 16 hours. After the reaction was completed, the solvent was evaporated under reduced pressure. The resulting residue was dissolved in a mixed solvent (12 mL) of ethyl acetate and methanol (1:2), 10% palladium-carbon (53 mg) was added, and the mixture was stirred at room temperature under a hydrogen atmosphere for 1 hour. After the reaction was completed, the reaction mixture was filtered through celite, the filtrate was washed with ethanol, and the solvent was evaporated under reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate:methanol, 10:1, v/v) to give the title compound (149 mg; yield, 81%) as a colorless oily substance.

Workup

  1. customto separate the layers
  2. customThe resulting organic layer was separated
  3. washwashed with saturated sodium chloride solution
  4. dry with materialdried with anhydrous sodium sulfate
  5. customthe solvent was evaporated under reduced pressure
  6. dissolutionThe resulting residue was dissolved in 1,4-dioxane (6 mL)
  7. stirringthe mixture was stirred at 100° C. under a nitrogen atmosphere for 16 hours
  8. customthe solvent was evaporated under reduced pressure
  9. dissolutionThe resulting residue was dissolved in a mixed solvent (12 mL) of ethyl acetate and methanol (1:2), 10% palladium-carbon (53 mg)
  10. additionwas added
  11. stirringthe mixture was stirred at room temperature under a hydrogen atmosphere for 1 hour
  12. filtrationthe reaction mixture was filtered through celite
  13. washthe filtrate was washed with ethanol
  14. customthe solvent was evaporated under reduced pressure
  15. customThe residue was purified by NH silica gel column chromatography (ethyl acetate

Sources & evidence

ORD record
ord-b86280dcbf0649fba3ac6b91d348aa58
Source dataset
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08476253B2

Reaction notes

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