Methylamine → HCID 178464136, compound
Reaction equation
Br.[Cl:2][C:3]1[CH:8]=[C:7]([Cl:9])[CH:6]=[CH:5][C:4]=1[C:10]1([OH:37])[C:18]2[C:13](=[CH:14][C:15]([C:23](O)=[O:24])=[CH:16][C:17]=2[C:19]([F:22])([F:21])[F:20])[N:12]([CH2:26][C@H:27]2[CH2:30][C@H:29]([N:31]([CH2:34][CH3:35])[CH2:32][CH3:33])[CH2:28]2)[C:11]1=[O:36].[CH3:38][NH2:39]>>[ClH:2].[CH3:38][NH:39][C:23]([C:15]1[CH:14]=[C:13]2[C:18]([C:10]([C:4]3[CH:5]=[CH:6][C:7]([Cl:9])=[CH:8][C:3]=3[Cl:2])([OH:37])[C:11](=[O:36])[N:12]2[CH2:26][C@H:27]2[CH2:30][C@H:29]([N:31]([CH2:34][CH3:35])[CH2:32][CH3:33])[CH2:28]2)=[C:17]([C:19]([F:20])([F:22])[F:21])[CH:16]=1)=[O:24]Participants
3
Procedure
The compound of Example 8 (200 mg, 0.32 mmol) and excess amount of methylamine were reacted in a similar manner to Example 9 to give the titled compound (75.0 mg, 40%).
Sources & evidence
- ORD record
- ord-a169e040e51840b5b2933031394c4c35
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07825155B2
Reaction notes
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