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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862141Generated: November 2, 2026

Boron tribromide → HCID 136164946, compound

https://huagongshe.com/reaction/1862141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 136164947HCID 136164947—
SolventEthyl AcetateHCID 8857—
ProductHCID 136164946HCID 13616494659%

Reaction Conditions

Temperature-78 °C

Reaction Steps

3-1H-Benzoimidazol-2-yl-6-(2-(2-methoxyethyl)-4-hydroxyphenyl)-1H-indazole, from Example 24(i), (99 mg, 0.26 mmol) was dissolved in EtOAc (20 mL) and cooled to −78° C. under argon. Boron tribromide was added dropwise, and the reaction was allowed to stir while warming to r.t over 3 h. The solution was diluted with EtOAc (60 mL) and washed with sat NaHCO3 and brine (20 mL each). Organics were dried (Na2SO4) and concentrated in vacuo. Purification by silica gel chromatography (THF) gave 56 mg (59%) of the title compound as a white solid. 1H NMR (300 MHz, DMSO-d6) δ 13.60 (s, 1H), 13.01 (s, 1H), 9.41 (s, 1H), 8.49 (d, 1H, J=8.4 Hz), 7.71 (br s, 1H), 7.51 (br s, 1H), 7.46 (s, 1H), 7.21 (app d, 3H, J=8.1 Hz), 7.08 (d, 1H, J=8.4 Hz), 6.77 (d, 1H, J=2.1 Hz), 6.69 (dd, 1H, J=8.1, 2.1 Hz), 4.57 (br s, 1H), 3.46 (t, 2H, J=7.2 Hz), 2.68 (t, 2H, J=7.2 Hz). MS (ES) [m+H]/z calc'd 371, found 371; [m−H]/z calc'd 369, found 369.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06534524B1
Source datasetuspto-grants-2003_03
ORD IDord-4edd30076abe472198cee7ed860740d2
Source noteuspto-grants-2003_03