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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436404Generated: October 30, 2026

(Diethylamino)sulfur trifluoride → HCID 25029412, compound

https://huagongshe.com/reaction/1436404

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantHCID 25029411HCID 25029411—
SolventDichloromethaneHCID 6344—
ProductHCID 25029412HCID 2502941234%

Reaction Conditions

Temperature25 °C

Reaction Steps

(4R)-3-[4-(4-Bromophenyl)-1,3-thiazol-2-yl]-4-(hydroxymethyl)-1,3-oxazolidin-2-one (0.71 g, 2.0 mmol), prepared in Example 71, was dissolved in 20 mL methylene chloride and cooled to 0° C. (Diethylamino)sulfur trifluoride (0.295 mL, 2.20 mmol) was added dropwise. The mixture was warmed to 25° C. and stirred for 2.5 h. The reaction was quenched with water and saturated NaHCO3 and the mixture was extracted with methylene chloride. The organics were combined and washed with water, brine, dried over anhydrous MgSO4, filtered and concentrated under reduced pressure. Flash chromatography (8% acetone/hexane) afforded the title compound (243 mg, 34%) as a white solid. mp 148-150° C. HRMS: calcd for C13H10BrFN2O2S+H+, 356.97031; found (ESI, [M+H]+), 356.9705. Analytical HPLC: retention time 10.2 min, 210-370 nm the Xterra® RP18 column, 3.5μ, 150×4.6 mm 40° C. 85/15-5/95 (Ammon. Form. Buff. pH 3.5/ACN+MeOH) for 10 min, hold 4 min, 1.2 mL/min 5 μL injection.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618990B2
Source datasetuspto-grants-2009_11
ORD IDord-4ac6340d3e7d4be5b9a375ae2ce8729d
Source noteuspto-grants-2009_11