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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68612Generated: October 29, 2026

Triethylamine → HCID 66868579, compound

https://huagongshe.com/reaction/68612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
Reactantt-Butyl 2-(2-(4-fluoro-3-(methylsulfonyl)phenyl)-4-((methylamino)methyl)phenoxy)acetateHCID 67528897—
SolventDichloromethaneHCID 6344—
ProductHCID 66868579HCID 6686857973.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To secondary amine 30 (150 mg, 0.35 mmol, 1 eq.) in dry DCM (15 mL) at 0° C. was added Et3N (3 mL) followed by dropwise addition of a DCM solution of 4-fluorobenzenesulfonyl chloride (90 mg, 0.42 mmol, 1.2 eq). After stirring at 0° C. for 20 min, the mixture was stirred at room temperature for 2 h. The reaction was extracted between DCM and water and the organic layer was washed with 1N HCl, saturated NaHCO3 solution, and brine, dried (Na2SO4), and concentrated in vacuo to give 150 mg (72%) of t-butyl 2-((4-fluoro-3-(methylsulfonyl)phenyl)-4-((4-fluoro-N-methylphenylsulfonamido)methyl)phenoxy)acetate (31) as oil which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822467B2
Source datasetuspto-grants-2014_09
ORD IDord-6217006d55254ab6952b54688f3fabdd
Source noteuspto-grants-2014_09