Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661975Generated: October 29, 2026

Dimethylformamide → 6-Bromo-5-(2-fluoro-4-nitrophenoxy)-1-methyl-1H-indazole

https://huagongshe.com/reaction/1661975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl methyl etherHCID 15413—
Reactant1-(2,4-Dibromo-5-(2-fluoro-4-nitrophenoxy)benzylidene)-2-methylhydrazineHCID 66767140—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product6-Bromo-5-(2-fluoro-4-nitrophenoxy)-1-methyl-1H-indazoleHCID 6676685380.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

1-(2,4-Dibromo-5-(2-fluoro-4-nitrophenoxy)benzylidene)-2-methylhydrazine (1.0 g, 2.2 mmol), cuprous chloride (22 mg, 0.2 mmol), potassium carbonate (0.638 g, 7.2 mmol), DMF (10 mL), and a stir bar are combined in a pressure tube under nitrogen. The cap is sealed and the tube is placed in an oil bath with stirring. The bath is heated to 100° C. over 30 min and held at 100° C. for 6 hours and then cooled to RT. The reaction mixture is poured into a separatory funnel containing MTBE (10 mL) and water (10 mL). The layers are separated and the aqueous layer is extracted with an additional portion of MTBE (10 mL). The organic layers are combined, and washed with water followed by saturated sodium chloride aqueous solution. The organic layer is dried over magnesium sulfate and concentrated to yield 0.70 g of crude product. The crude solid is dissolved in DCM and heptane, and then concentrated to remove DCM resulting in the formation of a slurry. The product is collected by filtration and dried under vacuum to give 6-bromo-5-(2-fluoro-4-nitrophenoxy)-1-methyl-1H-indazole as a solid (0.65 g, 79% yield). MS (m/z): 367.8 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030302B2
Source datasetuspto-grants-2011_10
ORD IDord-b68b829c946d4fda83d3f2a445dc9459
Source noteuspto-grants-2011_10