1,3,5-Trimethyl-3,7-diazabicyclo[3.3.1]nonan-9-ol → HCID 69226257, compound
Reaction equation
[C:1]([C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6](F)=[CH:5][CH:4]=1)#[N:2].[OH:14][CH:15]1[C:20]2([CH3:25])[CH2:21][N:22]([CH3:24])[CH2:23][C:16]1([CH3:26])[CH2:17][NH:18][CH2:19]2>>[OH:14][CH:15]1[C:16]2([CH3:26])[CH2:23][N:22]([CH3:24])[CH2:21][C:20]1([CH3:25])[CH2:19][N:18]([C:6]1[C:7]3[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=3)[C:3]([C:1]#[N:2])=[CH:4][CH:5]=1)[CH2:17]2Participants
3
Procedure
The title compound (3 mg, 8% yield) was prepared as described for 196MBT2-4 from 1-cyano-4-fluoronaphthalene (20 mg, 0.117 mmol) and 9-hydroxy-1,5,7-trimethyl-3,7-diazabicyclo[3.3.1]nonane (86 mg, 0.468 mmol).
Sources & evidence
- ORD record
- ord-6573876a409c449daf82c3284856dce9
- Source dataset
- uspto-grants-2007_09
- Patent number
- US07268232B2
Reaction notes
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