Methyl 6-[bis-(tert-butoxycarbonyl)amino]-2-hydroxy-3-(2-hydroxymethylfuran-3-yl)benzoate → Methyl 2-[bis-(tert-butyoxycarbonyl)amino]-6-hydroxybenzoate
Reaction equation
[C:1]([O:5][C:6]([N:8]([C:27]([O:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:28])[C:9]1[C:14]([C:15]([O:17][CH3:18])=[O:16])=[C:13]([OH:19])[C:12](C2C=COC=2CO)=[CH:11][CH:10]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].C(OC(N(C(OC(C)(C)C)=O)C1C=CC=C(OS(C2C=CC(C)=CC=2)(=O)=O)C=1C(OC)=O)=O)(C)(C)C>>[C:1]([O:5][C:6]([N:8]([C:27]([O:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:28])[C:9]1[CH:10]=[CH:11][CH:12]=[C:13]([OH:19])[C:14]=1[C:15]([O:17][CH3:18])=[O:16])=[O:7])([CH3:3])([CH3:4])[CH3:2]Participants
3
Procedure
Prepared by proceeding in a similar manner to Intermediate 4, starting from methyl 2-[bis-(tert-butoxycarbonyl)amino]-6-(4-methylbenzenesulfonyloxy)benzoate (Intermediate 56)
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-880f9489ba05458ab5836c2f49912551
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09290472B2
Reaction notes
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