Isopropyl isocyanate → HCID 68633079, compound
Reaction equation
[CH:1]([N:4]=[C:5]=[O:6])([CH3:3])[CH3:2].[Cl:7][C:8]1[CH:16]=[C:15]([Cl:17])[C:14]([O:18][CH3:19])=[C:13]2[C:9]=1[CH2:10][CH2:11][CH:12]2[NH:20][C:21]1[CH:30]=[CH:29][C:28]2[C:23](=[CH:24][CH:25]=[C:26]([NH2:31])[CH:27]=2)[N:22]=1>>[Cl:7][C:8]1[CH:16]=[C:15]([Cl:17])[C:14]([O:18][CH3:19])=[C:13]2[C:9]=1[CH2:10][CH2:11][CH:12]2[NH:20][C:21]1[CH:30]=[CH:29][C:28]2[C:23](=[CH:24][CH:25]=[C:26]([NH:31][C:5]([NH:4][CH:1]([CH3:3])[CH3:2])=[O:6])[CH:27]=2)[N:22]=1Participants
3
Procedure
The title compound was prepared in accordance with the general method described in example 3 from isopropyl isocyanate and rac-N2-(4,6-dichloro-7-methoxy-indan-1-yl)-quinoline-2,6-diamine; MS: m/e=460.6 (M+H+).
Sources & evidence
- ORD record
- ord-0ac2067c245b46d39dce85165becaa8f
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08183380B2
Reaction notes
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