Methylamine → HCID 10044051, compound
Reaction equation
[F:1][C:2]1[CH:24]=[CH:23][CH:22]=[C:21]([F:25])[C:3]=1[CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([N:12]2[C:16](=[O:17])[CH2:15][C@@H:14]([C:18](O)=[O:19])[CH2:13]2)=[CH:8][CH:7]=1.CN.[CH3:28][N:29](C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F>>[CH3:28][NH:29][C:18]([C@@H:14]1[CH2:15][C:16](=[O:17])[N:12]([C:9]2[CH:10]=[CH:11][C:6]([O:5][CH2:4][C:3]3[C:2]([F:1])=[CH:24][CH:23]=[CH:22][C:21]=3[F:25])=[CH:7][CH:8]=2)[CH2:13]1)=[O:19]Participants
4
Procedure
In an analogous manner to that described in Example 24f), the condensation of the (R)-1-[4-(2,6-difluoro-benzyloxy)-phenyl]-5-oxo-pyrrolidine-3-carboxylic acid with methylamine using HBTU as the condensation agent yields the (R)-1-[4-(2,6-difluoro-benzyloxy)-phenyl]-5-oxo-pyrrolidine-3-carboxylic acid methylamide as a white solid. MS: m/e=361 (M+H)+.
Sources & evidence
- ORD record
- ord-527fb8d6519b4ee98bca94bb2e6507af
- Source dataset
- uspto-grants-2006_05
- Patent number
- US07037935B2
Reaction notes
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