Formaldehyde → 7-Bromo-2-methyl-2H-indazole-3-methanol
Reaction equation
[Br:1][C:2]1[C:10]2[C:6](=[CH:7][N:8]([CH3:11])[N:9]=2)[CH:5]=[CH:4][CH:3]=1.C([N-]C(C)C)(C)C.[Li+].[O:20]1CCC[CH2:21]1.CCCCCCC.C(C1C=CC=CC=1)C.C=O>C1COCC1>[Br:1][C:2]1[C:10]2[C:6](=[C:7]([CH2:21][OH:20])[N:8]([CH3:11])[N:9]=2)[CH:5]=[CH:4][CH:3]=1Participants
6
Conditions
- Temperature
- 2.5 °C
Procedure
To a solution of 7-bromo-2-methyl-2H-indazole (6: R=Me; 0.578 g, 2.93 mmol) in 15 mL of THF at −78° C. was added a 2.0 M solution of lithium diisopropylamide in tetrahydrofuran/heptane/ethylbenzene (1.8 mL, 3.6 mmol). The yellow-orange solution was stirred at 0-5° C. for 15 m, then rechilled to −78° C. for 15 m. Paraformaldehyde (0.92 g) was added, and the orange mixture was rapidly stirred at −78° C. for 75 m then at room temperature for 100 m. The mixture was loaded onto silica gel and concentrated. Column chromatography (0→66% EtOAc/hexanes) afforded 0.662 g of impure (7-bromo-2-methyl-2H-indazol-3-yl)-methanol (14a).
Workup
- customrechilled to −78° C. for 15 m
- stirringthe orange mixture was rapidly stirred at −78° C. for 75 m
- customat room temperature
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-e6a56ffb61384ef388792ce4970a8650
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07365211B2
Reaction notes
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