HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916666Generated: November 2, 2026
Hydrogen Bromide → 5-Bromo-1-(2-(pyrrolidin-1-yl)ethyl)-1H-indazole
https://huagongshe.com/reaction/1916666
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 1-(2-Pyrrolidin-1-YL-ethyl)-1H-indazol-5-ylamine | HCID 11310777 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Bromo-1-(2-(pyrrolidin-1-yl)ethyl)-1H-indazole | HCID 57625541 | — |
Reaction Steps
1.00 g (4.34 mmol) 1-(2-pyrrolidin-1-yl-ethyl)-1H-indazol-5-ylamine is dissolved in 9.76 mL 48% hydrobromic acid and 9.76 mL water and the solution is cooled to 0° C. 2.5 M sodium nitrite solution (300 mg in 1.74 mL water) is slowly added dropwise. The reaction is stirred for 10 min at 0° C. and then a solution of 935 mg (6.51 mmol) CuBr in 3.42 mL 48% hydrobromic acid is added dropwise. The reaction is heated to 60° C. and stirred for one hour at this temperature. The mixture is diluted with water and the aqueous phase is extracted with EtOAc. The organic phase is discarded and the aqueous phase is made alkaline with saturated NaHCO3 solution. The aqueous phase is extracted with EtOAc and the organic phase is washed with water. The organic phase is dried over MgSO4 and the solvent is eliminated i.vac.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08618132B2 |
|---|
| Source dataset | uspto-grants-2013_12 |
|---|
| ORD ID | ord-ef632ad3988e451b9e13730e5e70c898 |
|---|
| Source note | uspto-grants-2013_12 |
|---|