Methylamine hydrochloride → HCID 71113180, compound
Reaction equation
[CH2:1]([C:3]([NH:9][C:10](=[O:29])[C:11]1[CH:16]=[CH:15][C:14]([C:17]([F:20])([F:19])[F:18])=[C:13]([O:21][CH2:22][CH:23]2[CH2:28][CH2:27][O:26][CH2:25][CH2:24]2)[N:12]=1)([CH2:7][CH3:8])[C:4]([OH:6])=O)[CH3:2].Cl.[CH3:31][NH2:32]>>[CH2:1]([C:3]([NH:9][C:10]([C:11]1[CH:16]=[CH:15][C:14]([C:17]([F:20])([F:18])[F:19])=[C:13]([O:21][CH2:22][CH:23]2[CH2:28][CH2:27][O:26][CH2:25][CH2:24]2)[N:12]=1)=[O:29])([C:4](=[O:6])[NH:32][CH3:31])[CH2:7][CH3:8])[CH3:2]Participants
3
Procedure
The title compound was synthesized in analogy to Example 1, using 2-ethyl-2-(6-((tetrahydro-2H-pyran-4-yl)methoxy)-5-(trifluoromethyl)picolinamido)butanoic acid and methanamine hydrochloride as starting materials. MS (EI): m/e=432.3 [M+H]+.
Sources & evidence
- ORD record
- ord-f71088f189ff41008baf4932f7303e33
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09321727B2
Reaction notes
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