Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295022Generated: October 30, 2026

Cyclohexene → 4-(2-allyl-7-fluoro-2H-indazol-3-yl)benzene-1,3-diol

https://huagongshe.com/reaction/1295022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexeneHCID 8079—
ReactantBoron tribromideHCID 25134—
Reactant2-allyl-3-(2,4-dimethoxyphenyl)-7-fluoro-2H-indazoleHCID 68882446—
Product4-(2-allyl-7-fluoro-2H-indazol-3-yl)benzene-1,3-diolHCID 13635846940.5%

Reaction Steps

Prepared according to Method D step C from 2-allyl-3-(2,4-dimethoxyphenyl)-7-fluoro-2H-indazole (0.057 g, 0.2 mmol), boron tribromide (0.150 mL, 1.6 mmol) and 1.0 mL of cyclohexene to give the product (0.023 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241791B2
Source datasetuspto-grants-2007_07
ORD IDord-98098d1e788f4394b7e21af7a8320944
Source noteuspto-grants-2007_07