Ethanol → HCID 178478666, compound
Reaction equation
C(O)C.[N+:4]([C:7]1[N:8]=[C:9]([CH:12]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:13]([N:15]2[CH2:19][CH2:18][CH2:17][CH2:16]2)=[O:14])[NH:10][CH:11]=1)([O-])=O.C(OCC)C.C(Cl)[Cl:32]>[Pd]>[ClH:32].[ClH:32].[NH2:4][C:7]1[N:8]=[C:9]([CH:12]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:13]([N:15]2[CH2:16][CH2:17][CH2:18][CH2:19]2)=[O:14])[NH:10][CH:11]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
Ethanol (200 mL) was added to a mixture of 2-(4-nitroimidazolyl)-2-phenyl-1-pyrrolidinylethan-1-one (3) (0.752 g, 2.8 mm) and 10% Pd on carbon (75 mg) in a Bradley hydrogenation apparatus. The stirred reaction mixture was subjected to a 60 psi H2 atmosphere and warmed to 60° C. After 2 hours, the reaction mixture was cooled to room temperature and the catalyst was removed by filtration. Anhydrous HCl gas was added to the filtered solution until saturation. The volatiles were then removed under vacuum to give a light yellow foam. Diethyl ether and methylene chloride (25:1) were added to the foam and the resulting mixture was stirred overnight to achieve crystallization. The resulting slurry was filtered and the cake was washed with diethyl ether. The cake was dried under vacuum to give 0.659 g (93%) of a yellow solid. LGD 208.
Workup
- customThe stirred reaction mixture
- temperaturethe reaction mixture was cooled to room temperature
- customthe catalyst was removed by filtration
- additionAnhydrous HCl gas was added to the filtered solution until saturation
- customThe volatiles were then removed under vacuum
- customto give a light yellow foam
- customcrystallization
- filtrationThe resulting slurry was filtered
- washthe cake was washed with diethyl ether
- customThe cake was dried under vacuum
Sources & evidence
- ORD record
- ord-179c39d1d1a24d9eb563ed7f46840ed9
- Source dataset
- uspto-grants-2004_12
- Patent number
- US06828331B1
Reaction notes
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