5-Methylpyrazin-2-amine → HCID 57504591, compound
Reaction equation
[Si:1]([O:8][C@@H:9]([CH2:13][O:14][CH3:15])[C:10]([OH:12])=O)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[CH3:16][C:17]1[N:18]=[CH:19][C:20]([NH2:23])=[N:21][CH:22]=1>>[Si:1]([O:8][C@@H:9]([CH2:13][O:14][CH3:15])[C:10]([NH:23][C:20]1[CH:19]=[N:18][C:17]([CH3:16])=[CH:22][N:21]=1)=[O:12])([C:4]([CH3:5])([CH3:6])[CH3:7])([CH3:2])[CH3:3]Participants
3
Procedure
C6a was prepared in an analogous fashion to C4d from (S)-2-(tert-butyldimethylsilyloxy)-3-methoxypropanoic acid C4c and 5-methylpyrazine-2-amine (CAS 5521-58-4).
Sources & evidence
- ORD record
- ord-aa4c9dd43bac445888c73db798c2a002
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08143263B2
Reaction notes
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