4-(Methylamino)tricyclo[3.3.1.13,7]decan-1-ol → HCID 25242342, compound
Reaction equation
[O:1]1[CH2:6][CH2:5][CH:4]([O:7][C:8]2[CH:9]=[C:10]([CH:14]=[CH:15][CH:16]=2)[C:11]([OH:13])=O)[CH2:3][CH2:2]1.[OH:17][C:18]12[CH2:27][CH:22]3[CH2:23][CH:24]([CH2:26][CH:20]([CH:21]3[NH:28][CH3:29])[CH2:19]1)[CH2:25]2>>[OH:17][C:18]12[CH2:27][CH:22]3[CH2:23][CH:24]([CH2:26][CH:20]([CH:21]3[N:28]([CH3:29])[C:11](=[O:13])[C:10]3[CH:14]=[CH:15][CH:16]=[C:8]([O:7][CH:4]4[CH2:3][CH2:2][O:1][CH2:6][CH2:5]4)[CH:9]=3)[CH2:19]1)[CH2:25]2Participants
3
Procedure
Prepared from 3-(tetrahydro-pyran-4-yloxy)-benzoic acid and 1-hydroxy-4-methylaminoadamantane. LC-MS (m/z): 387 (M+2).
Sources & evidence
- ORD record
- ord-3e1d091cff5a4406a77c3d4287798262
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08809540B2
Reaction notes
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