Reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]2[CH:8]3[CH2:13][CH2:12][N:11]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:10][CH:9]3[O:21][C:4]=2[CH:3]=1.[CH3:22]OC1C=CC2C3(C)CCN=CC3OC=2C=1>>[OH:1][C:2]1[CH:7]=[CH:6][C:5]2[C:8]3([CH3:22])[CH2:13][CH2:12][N:11]([C:14]([O:16][C:17]([CH3:18])([CH3:20])[CH3:19])=[O:15])[CH2:10][CH:9]3[O:21][C:4]=2[CH:3]=1Participants
3
Reactant 2
Product 1
Procedure
Synthesized as described for tert-butyl 7-hydroxy-3,4,4a,9a-tetrahydro[1]benzofuro[2,3-c]pyridine-2(1H)-carboxylate starting from 7-Methoxy-4a-methyl-3,4,4a,9a-tetrahydro[1]benzofuro[2,3-c]pyridine.
Workup
- customSynthesized
Sources & evidence
- ORD record
- ord-2f94afe45db34c8f8632448499cb9131
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765779B2
Linked notes
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