(2-Chloro-3,4-difluorophenyl)methanamine hydrochloride → N-[(2-chloro-3,4-difluorophenyl)methyl]-1-ethyl-4,4-dimethyl-5-oxoprolinamide
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH2:9][NH:10][C:11](=[O:22])[C@@H:12]1[CH2:16][C:15]([CH3:18])([CH3:17])[C:14](=[O:19])[N:13]1[CH2:20][CH3:21].Cl.ClC1C([F:31])=C(F)C=CC=1CN>>[Cl:1][C:2]1[C:7]([F:31])=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH2:9][NH:10][C:11](=[O:22])[C@@H:12]1[CH2:16][C:15]([CH3:17])([CH3:18])[C:14](=[O:19])[N:13]1[CH2:20][CH3:21]Participants
3
Procedure
N-[(2-chloro-3,4-difluorophenyl)methyl]-1-ethyl-4,4-dimethyl-5-oxoprolinamide was prepared in a manner analogous to that described above for the synthesis of N-[(2-chloro-4-fluorophenyl)methyl]-1-ethyl-4,4-dimethyl-5-oxoprolinamide (E130) but using [(2-chloro-3,4-difluorophenyl)methyl]amine hydrochloride (prepared as described above for Example 36) in the place of [(2-chloro-4-fluorophenyl)methyl]amine.
Sources & evidence
- ORD record
- ord-eabf514edfee4aa187bec4ee6b3c3097
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07718693B2
Reaction notes
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