Potassium Carbonate → HCID 178517846, compound

HRID 51308

Reaction equation

HRID 51308 reaction equation
[NH:1]1[CH2:6][CH2:5][O:4][CH2:3][C:2]1=[O:7].[N+]([O-])([O-])=O.[Ce+4].[NH4+:13].[N+]([O-])([O-])=O.[N+]([O-])([O-])=O.[N+]([O-])([O-])=O.[N+]([O-])([O-])=O.C(=O)([O-])[O-].[K+].[K+].C(O[CH2:40][CH3:41])(=O)C.CO.[CH2:44]([NH:46][CH2:47]C)C>O.C(#N)C>[NH:46]1[CH:47]=[C:40]([CH2:41][C@@H:3]2[O:4][CH2:5][CH2:6][NH:1][C:2]2=[O:7])[N:13]=[CH:44]1

Participants

7

Conditions

Temperature
40 °C

Procedure

A mixture of the protected morpholinone of Preparation 53 (500 mg, 1.66 mmol), and ammonium cerium (IV) nitrate (2.5 g, 4.5 mmol) in water (6 ml) and acetonitrile (6 ml) was stirred at 40° C. for 18 hours. Potassium carbonate (1.5 g) was added and the mixture was stirred for 10 minutes then adsorbed onto silica gel. The product was isolated by column chromatography on silica gel using ethyl acetate:methanol:diethylamine (96:2:2 to 80:10:10) and was further purified by column chromatography on silica gel using dichloromethane:methanol (90:10 to 85:15) to afford the title compound, 240 mg. 1H-NMR (CD3OD, 400 MHz) δ: □3.02-3.42 (m, 4H), 3.78 (m, 1H0, 4.00 (m, 1H), 4.38 (m, 1H), 6.75 (s, 1H), 7.78 (s, 1H). HRMS: m/z (ES+) 182.0924 [MH+]

Workup

  1. stirringthe mixture was stirred for 10 minutes
  2. customThe product was isolated by column chromatography on silica gel
  3. customwas further purified by column chromatography on silica gel

Sources & evidence

ORD record
ord-1162d8b81ce0495ab8ba0da37aef36a3
Source dataset
uspto-grants-2004_03
Patent number
US06713496B2

Linked notes

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