Benzylamine → HCID 87644076, compound
Reaction equation
[C:1]([CH2:3][N:4]([C:16]1[CH:21]=[CH:20][N:19]=[C:18](F)[N:17]=1)[C:5](=[O:15])[C@H:6]([CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[NH2:7])#[N:2].[CH2:23]([NH2:30])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>>[CH2:23]([NH:30][C:18]1[N:17]=[C:16]([N:4]([CH2:3][C:1]#[N:2])[C:5](=[O:15])[C@H:6]([CH2:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[NH2:7])[CH:21]=[CH:20][N:19]=1)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1Participants
3
Procedure
The title compound was prepared from the product from step (ii) (0.2 g) and benzylamine (0.37 ml) by the method of example 1 step (iv). Yield 0.11 g.
Sources & evidence
- ORD record
- ord-40aedc3e684744e7b81d2e15e72d9d73
- Source dataset
- uspto-grants-2009_10
- Patent number
- US07605159B2
Reaction notes
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