Dichloromethane → 6-Bromo-4-nitro-2-(tetrahydro-2H-pyran-2-yl)-2H-indazole
Reaction equation
[Br:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[N:7][NH:8]2)=[C:4]([N+:11]([O-:13])=[O:12])[CH:3]=1.C(O)(C(F)(F)F)=O.C(Cl)Cl.C(=O)(O)[O-].[Na+].[O:29]1[CH:34]=[CH:33][CH2:32][CH2:31][CH2:30]1>>[Br:1][C:2]1[CH:3]=[C:4]([N+:11]([O-:13])=[O:12])[C:5]2[C:9]([CH:10]=1)=[N:8][N:7]([CH:30]1[CH2:31][CH2:32][CH2:33][CH2:34][O:29]1)[CH:6]=2Participants
6
Procedure
To 6-bromo-4-nitro-1H-indazole (10 g) in dihydropyran (100 ml) was added TFA (0.068 ml) and the reaction was heated for 1.5 h at reflux. After cooling, DCM (180 ml) and saturated sodium bicarbonate solution (50 ml) was added and stirred for 10 min. The DCM was separated from the aq which was re-washed with DCM (70 ml). The combined organic layers were passed through a hydrophobic frit and evaporated to dryness. The residual solid was triturated with ether then filtered. The solid material was dissolved in DCM and purified by chromatography on silica on the ISCO Companion, using an isocratic gradient of DCM. Purified fractions were combined and evaporated to dryness to afford the title compound, 7.78 g.
Workup
- temperaturethe reaction was heated for 1.5 h
- temperatureat reflux
- temperatureAfter cooling
- customThe DCM was separated from the aq which
- washwas re-washed with DCM (70 ml)
- customevaporated to dryness
- customThe residual solid was triturated with ether
- filtrationthen filtered
- dissolutionThe solid material was dissolved in DCM
- custompurified by chromatography on silica on the ISCO Companion
- customevaporated to dryness
Sources & evidence
- ORD record
- ord-30df097a7307494eb8d09f158633fb60
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09326987B2
Reaction notes
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