Glycine → HCID 24780550, compound
Reaction equation
C(O[C:6]([C:8]1[N:9]=[C:10]([C:29]#[N:30])[C:11]2[C:16]([C:17]=1[OH:18])=[CH:15][CH:14]=[C:13]([O:19][C:20]1[CH:28]=[CH:27][C:23]3[O:24][CH2:25][O:26][C:22]=3[CH:21]=1)[CH:12]=2)=[O:7])CCC.[NH2:31][CH2:32][C:33]([OH:35])=[O:34]>>[O:24]1[C:23]2[CH:27]=[CH:28][C:20]([O:19][C:13]3[CH:12]=[C:11]4[C:16]([C:17]([OH:18])=[C:8]([C:6]([NH:31][CH2:32][C:33]([OH:35])=[O:34])=[O:7])[N:9]=[C:10]4[C:29]#[N:30])=[CH:15][CH:14]=3)=[CH:21][C:22]=2[O:26][CH2:25]1Participants
3
Procedure
Prepared in analogy to example 31h from 7-(benzo[1,3]dioxol-5-yloxy)-1-cyano-4-hydroxy-isoquinoline-3-carboxylic acid butyl ester and glycine. ESI MS (m/z): 406 (M−H)−.
Sources & evidence
- ORD record
- ord-4c2798d284ee44ca9e10eddc8eb5ebb5
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08759373B2
Reaction notes
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