2-Butanamine, 1-methoxy- → HCID 10018721, 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].[CH3:20][O:21][CH2:22][CH:23]([NH2:26])[CH2:24][CH3:25]>>[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1[NH:26][CH:23]([CH2:22][O:21][CH3:20])[CH2:24][CH3:25])=[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 1-methoxy-2-aminobutane 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-f9e8147c576d46bca8011188fee01547
- Source dataset
- uspto-grants-2006_03
- Patent number
- US07009053B2
Reaction notes
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