HCID 18719787, compound → (2S)-3H-4-Azaspiro[bicyclo[2.2.2]octane-2,2-furo[2,3-B]pyridin]-5-amine
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]2[CH2:12][C@@:11]3([CH:17]4[CH2:18][CH2:19][N:14]([CH2:15][CH2:16]4)[CH2:13]3)[O:10][C:7]2=[N:8][CH:9]=1)([O-])=O>CO>[NH2:1][C:4]1[CH:5]=[C:6]2[CH2:12][C@@:11]3([CH:17]4[CH2:16][CH2:15][N:14]([CH2:19][CH2:18]4)[CH2:13]3)[O:10][C:7]2=[N:8][CH:9]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The enantiomer (S)-(+)-5'nitrospiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[2,3-b]pyridine] (6.85 g, 26.2 mmol) treated in the same way as described in example 8A in ammoniated methanol provided the title compound (5.55 g, 24 mmol, 92%): electrospray MS (m/z, relative intensity) 232 ([MH]+, 100).
Sources & evidence
- ORD record
- ord-809af71e5cee481e842cd4e0ac96d3c2
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06110914
Reaction notes
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