Sodium Iodide → HCID 67141748, compound
Reaction equation
[CH3:1][O:2][C:3]([CH:5]1[CH2:7][N:6]1[S:8]([CH:11]([CH3:13])[CH3:12])(=[O:10])=[O:9])=[O:4].[I-].[Na+].[Cl:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[N:23]=[C:24]=[O:25]>>[CH3:1][O:2][C:3]([CH:5]1[CH2:7][N:6]([S:8]([CH:11]([CH3:12])[CH3:13])(=[O:9])=[O:10])[C:24](=[O:25])[N:23]1[C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=1[Cl:16])=[O:4]Participants
4
Procedure
In analogy to example 1, the crude 1-(propane-2-sulfonyl)-aziridine-2-carboxylic acid methyl ester from example 82, step 1 was reacted with sodium iodide and 2-chlorophenyl isocyanate to give (RS)-3-(2-chloro-phenyl)-2-oxo-1-(propane-2-sulfonyl)-imidazolidine-4-carboxylic acid methyl ester as a light yellow oil. MS: 361.1 ([M+H]+)
Sources & evidence
- ORD record
- ord-6dfb11c9588544ef8cb2285298b89bce
- Source dataset
- uspto-grants-2009_12
- Patent number
- US07625902B2
Reaction notes
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