HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067976Generated: October 26, 2026
Dimethyl Sulfoxide → 1-(4-chloro-phenyl)-5-methyl-1H-pyrazole-4-carboxylic acid [1-(5-methanesulfonyl-pyridin-3-yl)-butyl]-amide
https://huagongshe.com/reaction/2067976
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | Sodium methanesulfinate | HCID 2733271 | — |
| Reactant | 1-(4-Chloro-phenyl)-5-methyl-1H-pyrazole-4-carboxylic acid [1-(5-bromo-pyridin-3-yl)-butyl]-amide | HCID 44480597 | — |
| Catalyst | copper(II) trifluoromethanesulfonate | HCID 2734996 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(4-chloro-phenyl)-5-methyl-1H-pyrazole-4-carboxylic acid [1-(5-methanesulfonyl-pyridin-3-yl)-butyl]-amide | HCID 44480600 | 30.5% |
Reaction Steps
1-(4-Chloro-phenyl)-5-methyl-1H-pyrazole-4-carboxylic acid [1-(5-bromo-pyridin-3-yl)-butyl]-amide (100 mg, 0.22 mmol), copper(II) triflate (81 mg, 0.22 mmol), sodium methylsulfinate (80 mg, 0.67 mmol) are added to a reaction vial with a septum top which is then evacuated and filled with nitrogen for 3 cycles. DMSO (1 mL) and N,N′-dimethylethylenediamine (71 μL, 0.67 mmol) are added and the reaction is heated at 100° C. for 30 hours. The resultant mixture is cooled to room temperature, diluted with EtOAc (50 mL), and washed with saturated aqueous ammonium chloride (2×25 mL), saturated aqueous sodium bicarbonate (25 mL) and brine (25 mL). The combined organic layers are dried over magnesium sulfate, filtered and concentrated in vacuo. The crude material is purified by preparative reverse phase HPLC (eluted with 10 to 95% CH3CN/H2O and 0.1% TFA as additive) to afford 1-(4-chloro-phenyl)-5-methyl-1H-pyrazole-4-carboxylic acid [1-(5-methanesulfonyl-pyridin-3-yl)-butyl]-amide as a colorless foam (30 mg, 30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08293917B2 |
|---|
| Source dataset | uspto-grants-2012_10 |
|---|
| ORD ID | ord-4f44820043514a64861dea8f65e46e79 |
|---|
| Source note | uspto-grants-2012_10 |
|---|