D-Alanine → HCID 135879605, compound
Reaction equation
C(O[C:4]([C:6]1[C:7]([OH:21])=[C:8]2[C:14]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)=[N:13][O:12][C:9]2=[CH:10][N:11]=1)=[O:5])C.[NH2:22][C@@H:23]([C:25]([OH:27])=[O:26])[CH3:24]>>[OH:21][C:7]1[C:6]([C:4]([NH:22][C@H:23]([CH3:24])[C:25]([OH:27])=[O:26])=[O:5])=[N:11][CH:10]=[C:9]2[O:12][N:13]=[C:14]([C:15]3[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=3)[C:8]=12Participants
3
Procedure
Prepared in analogy to Example 11 from 4-hydroxy-3-phenyl-isoxazolo[5,4-c]pyridine-5-carboxylic acid ethyl ester and D-alanine; ESI MS (m/z): 328.20 (M+H+); 326.16 (M−H+).
Sources & evidence
- ORD record
- ord-df3ad9b4dcff4f7fa26261e572b8fccb
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08269008B2
Reaction notes
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