Methyl 2-amino-6-hydroxybenzoate → Methyl 2-[bis-(tert-butoxycarbonyl)amino]-6-(4-methylbenzenesulfonyloxy)-benzoate
Reaction equation
[C:1]([O:5][C:6]([N:8]([C:37]([O:39][C:40]([CH3:43])([CH3:42])[CH3:41])=[O:38])[C:9]1[C:14]([C:15]([O:17][CH3:18])=[O:16])=[C:13]([O:19][S:20]([C:23]2[CH:28]=[CH:27][C:26]([CH3:29])=[CH:25][CH:24]=2)(=[O:22])=[O:21])[C:12](C2C=COC=2C=O)=[CH:11][CH:10]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].NC1C=CC=C(O)C=1C(OC)=O>>[C:40]([O:39][C:37]([N:8]([C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])[C:9]1[CH:10]=[CH:11][CH:12]=[C:13]([O:19][S:20]([C:23]2[CH:24]=[CH:25][C:26]([CH3:29])=[CH:27][CH:28]=2)(=[O:22])=[O:21])[C:14]=1[C:15]([O:17][CH3:18])=[O:16])=[O:38])([CH3:42])([CH3:43])[CH3:41]Participants
3
Procedure
Prepared by proceeding in a similar manner to Intermediate 6, starting from methyl 2-amino-6-hydroxybenzoate (prepared according to Comess et al, US2004 0167128)
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-ad7cd940fccd47ff98eedf6e31853eca
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09290472B2
Reaction notes
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