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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Tetra-n-butylammonium tribromide | HCID 23500184 | — |
| Reactant | 3-methyl-1-(toluene-4-sulfonyl)-1H-indazol-6-ylamine | HCID 59377782 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 5-bromo-3-methyl-1-(toluene-4-sulfonyl)-1H-indazol-6-ylamine | HCID 59377801 | 147.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08153809B2 |
|---|
| Source dataset | uspto-grants-2012_04 |
|---|
| ORD ID | ord-913038bc785744b7840714c7b888a72d |
|---|
| Source note | uspto-grants-2012_04 |
|---|