Potassium Carbonate → HCID 22346208, compound

HRID 1293046Notes

Reaction equation

HRID 1293046 reaction equation
I[CH:2]1[CH2:6][CH2:5][CH2:4][CH2:3]1.C(=O)([O-])[O-].[K+].[K+].[CH:13]1([NH:18][CH2:19][CH2:20][NH:21][C:22](=[O:28])[O:23][C:24]([CH3:27])([CH3:26])[CH3:25])[CH2:17][CH2:16][CH2:15][CH2:14]1>>[NH3:18].[CH:2]1([N:18]([CH:13]2[CH2:14][CH2:15][CH2:16][CH2:17]2)[CH2:19][CH2:20][NH:21][C:22](=[O:28])[O:23][C:24]([CH3:27])([CH3:26])[CH3:25])[CH2:6][CH2:5][CH2:4][CH2:3]1

Participants

5

Conditions

Temperature
60 °C

Procedure

Iodocyclopentane (1.68 g, 8.6 mmol) was added to a suspension of potassium carbonate (1.8 g, 13.2 mmol) and tert-butyl 2-[cyclopentylamino]ethylcarbamate (1.5 g, 6.6 mmol) (Preparation 53) in N′,N′-dimethylformamide (10 ml). The reaction mixture was stirred at 60° C. for 72 hours. The reaction mixture was allowed to cool and was then partitioned between ethyl acetate (50 ml) and water (50 ml). The ethyl acetate layer was washed with brine (30 ml) and dried over anhydrous magnesium sulphate. The solvent was removed to give a residue that was purified by chromatography on silica gel eluting with dichloromethane:methanol (98:2 by volume) increasing in polarity to dichloromethane:methanol:0.88 concentrated aqueous ammonia (90:10:1 by volume) to give the title compound (64 mg) as a brown oil.

Workup

  1. temperatureto cool
  2. customwas then partitioned between ethyl acetate (50 ml) and water (50 ml)
  3. washThe ethyl acetate layer was washed with brine (30 ml)
  4. dry with materialdried over anhydrous magnesium sulphate
  5. customThe solvent was removed
  6. customto give a residue that
  7. customwas purified by chromatography on silica gel eluting with dichloromethane:methanol (98:2 by volume)
  8. temperatureincreasing in polarity to dichloromethane

Sources & evidence

ORD record
ord-abee277319aa44b9be62b3b5349ff983
Source dataset
uspto-grants-2007_07
Patent number
US07238676B2

Reaction notes

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