6-Methoxy-2-naphthol → 9-(6-Methoxy-Naphthalen-2-yloxy)-3-aza-spiro[5.5]undecane
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([OH:13])[CH:7]=[CH:6]2.C(OC([N:21]1[CH2:26][CH2:25][C:24]2([CH2:31][CH2:30][CH:29](O)[CH2:28][CH2:27]2)[CH2:23][CH2:22]1)=O)(C)(C)C>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([O:13][CH:29]1[CH2:30][CH2:31][C:24]3([CH2:25][CH2:26][NH:21][CH2:22][CH2:23]3)[CH2:27][CH2:28]1)[CH:7]=[CH:6]2Participants
3
Procedure
Was prepared according to method A from 6-methoxy-2-naphthol and 9-hydroxy-3-aza-spiro[5.5]undecane-3-carboxylic acid tert-butyl ester.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-e30f0440750043aeacb89d5ea4662e26
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08049012B2
Reaction notes
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