2-Amino-4-bromobenzoic acid → 6-Bromo-1,2-dihydro-3H-indazol-3-one
Reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:9]([OH:11])=O)=[C:6]([CH:8]=1)[NH2:7].BrC1C=CC=C2C=1C(O)=[N:16]N2>>[Br:1][C:2]1[CH:8]=[C:6]2[C:5]([C:9]([OH:11])=[N:16][NH:7]2)=[CH:4][CH:3]=1Participants
3
Procedure
6-Bromo-1H-indazol-3-ol CCVII was prepared from 5-bromo-2-carboxyaniline (JOC, 1997, 62, 1240) using the procedure described for preparation of 4-Bromo-1H-indazol-3-ol CLXXXIII (Example 37).
Sources & evidence
- ORD record
- ord-d7711fe1ee20416eb370bd5cb82417e8
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07803830B2
Reaction notes
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