Methylamine → HCID 67990211, compound
Reaction equation
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([CH:14]2[O:32][C:17]3=[CH:18][N:19]=[C:20]([C:22]4[CH:27]=[CH:26][C:25]([C:28]([OH:30])=O)=[CH:24][C:23]=4[F:31])[CH:21]=[C:16]3[CH2:15]2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH3:33][NH2:34]>>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([CH:14]2[O:32][C:17]3=[CH:18][N:19]=[C:20]([C:22]4[CH:27]=[CH:26][C:25]([C:28](=[O:30])[NH:34][CH3:33])=[CH:24][C:23]=4[F:31])[CH:21]=[C:16]3[CH2:15]2)[CH2:10][CH2:9]1)=[O:7])([CH3:3])([CH3:2])[CH3:4]Participants
3
Procedure
The title compound is prepared from 4-[5-(4-carboxy-2-fluoro-phenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl ester and methylamine following a procedure analogous to that described in Example 26. LC (method 7): tR=1.25 min; Mass spectrum (ESI+): m/z=456 [M+H]+.
Sources & evidence
- ORD record
- ord-18006d595b004355b04073ea71aed2b6
- Source dataset
- uspto-grants-2014_03
- Patent number
- US08669271B2
Reaction notes
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