Diethyl iminodiacetate → HCID 86595477, compound
Reaction equation
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([OH:12])=[C:4]([C:13]([OH:15])=O)[N:3]=1.C([O:18][C:19](=[O:28])[CH2:20][NH:21][CH2:22][C:23]([O:25]CC)=[O:24])C>>[C:19]([CH2:20][N:21]([CH2:22][C:23]([OH:25])=[O:24])[C:13]([C:4]1[N:3]=[C:2]([Cl:1])[C:11]2[C:6]([C:5]=1[OH:12])=[CH:7][CH:8]=[CH:9][CH:10]=2)=[O:15])([OH:28])=[O:18]Participants
3
Procedure
Prepared from 1-chloro-4-hydroxy-isoquinoline-3-carboxylic acid and (ethoxycarbonylmethyl-amino)-acetic acid ethyl ester analogously to Example D-49: MS-(+)-ion: 339.0 amu.
Sources & evidence
- ORD record
- ord-c2359daf864c4169aae4e41440a9be94
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07323475B2
Reaction notes
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