Imidazole-1-acetic acid → HCID 68914894, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:11]=1[CH:10]([NH:12][C:13]1[CH:22]=[CH:21][C:20]3[C:15](=[CH:16][CH:17]=[C:18]([NH2:23])[CH:19]=3)[N:14]=1)[CH2:9][CH2:8]2.[N:24]1([CH2:29][C:30](O)=[O:31])[CH:28]=[CH:27][N:26]=[CH:25]1>>[N:24]1([CH2:29][C:30]([NH:23][C:18]2[CH:19]=[C:20]3[C:15](=[CH:16][CH:17]=2)[N:14]=[C:13]([NH:12][CH:10]2[C:11]4[C:7](=[CH:6][CH:5]=[CH:4][C:3]=4[O:2][CH3:1])[CH2:8][CH2:9]2)[CH:22]=[CH:21]3)=[O:31])[CH:28]=[CH:27][N:26]=[CH:25]1Participants
3
Procedure
The title compound was prepared in accordance with the general method described in example 6 from rac-N2-(7-methoxy-indan-1-yl)-quinoline-2,6-diamine and imidazol-1-yl-acetic acid; MS: m/e=414.3 (M+H+).
Sources & evidence
- ORD record
- ord-d0c9362166314f6e8ef03006e3ff3864
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08188284B2
Reaction notes
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