Isopropylamine → HCID 10468524, compound
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1Cl)=[CH:13][CH:12]=[CH:11][C:10]=2[N+:17]([O-])=O)=[O:5])[CH3:2].[CH:20]([NH2:23])([CH3:22])[CH3:21]>>[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1[NH:23][CH:20]([CH3:22])[CH3:21])=[CH:13][CH:12]=[CH:11][C:10]=2[NH2:17])=[O:5])[CH3:2]Participants
3
Procedure
The compound prepared in Example 3 was reacted with isopropylamine according to the method as described in Example 4 and the obtained compound was treated as described in Example 14 to prepare the title compound (yield 80%).
Workup
- additionthe obtained compound was treated
Sources & evidence
- ORD record
- ord-1fb38f6351184ac295c1cdb0fb5fe284
- Source dataset
- uspto-grants-2006_03
- Patent number
- US07009053B2
Reaction notes
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