Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691806Generated: November 1, 2026

Methanol → 5-bromo-3-methyl-1-(toluene-4-sulfonyl)-1H-indazol-6-ylamine

https://huagongshe.com/reaction/1691806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTetra-n-butylammonium tribromideHCID 23500184—
Reactant3-methyl-1-(toluene-4-sulfonyl)-1H-indazol-6-ylamineHCID 59377782—
Solvent1,2-DichloroethaneHCID 11—
Product5-bromo-3-methyl-1-(toluene-4-sulfonyl)-1H-indazol-6-ylamineHCID 59377801147.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

3-Methyl-1-(toluene-4-sulfonyl)-1H-indazol-6-ylamine (301 mg, 1.0 mmol) was dissolved in 1,2-dichloroethane (80 ml) and methanol (40 ml) at room temperature. The mixture was heated to 80° C. and then the tetrabutylammonium tribromide (1.0 eq, 482 mg) was added. Stirring was continued for 10 minutes, and then the mixture was partitioned between diethyl ether and saturated aqueous sodium sulfite solution. The organic layer was separated, washed with water, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography (gradient 9:1 to 4:1 hexanes/ethyl acetate) to give 5-bromo-3-methyl-1-(toluene-4-sulfonyl)-1H-indazol-6-ylamine (280 mg, 73.7%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153809B2
Source datasetuspto-grants-2012_04
ORD IDord-913038bc785744b7840714c7b888a72d
Source noteuspto-grants-2012_04