Isopropyl isocyanate → HCID 68632943, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH3:24])[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.[CH:25]([N:28]=[C:29]=[O:30])([CH3:27])[CH3:26]>>[CH:25]([NH:28][C:29]([NH:23][C:18]1[CH:19]=[C:20]2[C:15](=[CH:16][CH:17]=1)[N:14]=[C:13]([NH:12][CH:10]1[C:11]3[C:7](=[CH:6][C:5]([CH3:24])=[CH:4][C:3]=3[O:2][CH3:1])[CH2:8][CH2:9]1)[CH:22]=[CH:21]2)=[O:30])([CH3:27])[CH3:26]Participants
3
Procedure
The title compound was prepared in accordance with the general method described in example 3 from rac-N2-(7-methoxy-5-methyl-indan-1-yl)-quinoline-2,6-diamine and isopropyl isocyanate; MS: m/e=405.6 (M+H+).
Sources & evidence
- ORD record
- ord-15ebfbf4a5614e1fa4804c7bde75516d
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08183380B2
Reaction notes
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