Methoxyacetic Acid → HCID 68915825, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:12]=1[CH:11]([NH:13][C:14]1[CH:23]=[CH:22][C:21]3[C:16](=[CH:17][CH:18]=[C:19]([NH2:24])[CH:20]=3)[N:15]=1)[CH2:10][CH2:9][CH2:8]2.[CH3:25][O:26][CH2:27][C:28](O)=[O:29]>>[CH3:25][O:26][CH2:27][C:28]([NH:24][C:19]1[CH:20]=[C:21]2[C:16](=[CH:17][CH:18]=1)[N:15]=[C:14]([NH:13][CH:11]1[C:12]3[C:7](=[CH:6][CH:5]=[CH:4][C:3]=3[O:2][CH3:1])[CH2:8][CH2:9][CH2:10]1)[CH:23]=[CH:22]2)=[O:29]Participants
3
Procedure
The title compound was prepared in accordance with the general method 14 described in example 119 from rac-N2-(8-methoxy-1,2,3,4-tetrahydro-naphthalen-1-yl)-quinoline-2,6-diamine and methoxyacetic acid; MS: m/e=392.3 (M+H+).
Sources & evidence
- ORD record
- ord-cbda732e8ca243559da6a0a1dd8e3047
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08183380B2
Reaction notes
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