HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540764Generated: October 30, 2026
(Diethylamino)sulfur trifluoride → HCID 52914041, compound
https://huagongshe.com/reaction/540764
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 52914040 | HCID 52914040 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 52914041 | HCID 52914041 | 35% |
Reaction Steps
N-ethyl-N-(trifluoro-λ4-sulfanyl)ethanamine (DAST, 0,021 mL, 0.16 mmol, 1.3 equiv) was added to a solution of N-[1-(3-{1-ethyl-5-[4-(hydroxymethyl)phenoxy]-1H-pyrazol-3-yl}phenyl)-1-methylethyl]-2,2,2-trifluoroethanesulfonamide (62 mg, 0.13 mmol, 1 equiv) in dichloromethane (1.2 mL) at −78° C. The reaction mixture was stirred at −78° C. for 5 minutes, then saturated sodium hydrogencarbonate was added. The crude mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride solution, and the washed solution was dried over sodium sulfate. The dried solution was filtered, and the filtrate was concentrated. The residue was purified by flash-column chromatography (hexanes, grading to 50% ethyl acetate-hexanes) to afford N-[1-(3-{1-ethyl-5-[4-(fluoromethyl)phenoxy]-1H-pyrazol-3-yl}phenyl)-1-methylethyl]-2,2,2-trifluoroethanesulfonamide (22 mg, 35%). Calcd (M+1)+: 500.2. Found: 500.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08871796B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-77c5b35e91264b52ab4d7e562f30624f |
|---|
| Source note | uspto-grants-2014_10 |
|---|