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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416199Generated: November 2, 2026

Ammonium Chloride → HCID 22638594, compound

https://huagongshe.com/reaction/2416199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(Bromomethyl)-4-fluoro-1-nitrobenzeneHCID 10561643—
ReactantHCID 22638557HCID 22638557—
SolventTolueneHCID 1140—
ProductHCID 22638594HCID 22638594—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Methyl 2-[2-(2-ethyl-4-pyridyl)-1,3-thiazole-4-yl]acetate (520 mg, 2.0 mmol) (Example 12(a)) was dissolved in toluene and the solution was concentrated by rotary evaporation. This procedure was repeated, and the dry residue was dissolved in 18 mL anhydrous THF (18 mL). The solution was cooled to −78° C., and LHMDS (2.1 mL, 1.0 M in THF, Aldrich) was added slowly via a syringe. To the resulting red solution, 5-fluoro-2-nitrobenzyl bromide (400 mg, 1.7 mmol) was added as a solid in one portion. The reaction was warmed slowly to RT over 4 h. Saturated aqueous NH4Cl (50 mL) was added, and the mixture was extracted with 100 mL of EtOAc. The organic layer was separated, washed with H2O (100 mL), dried (Na2SO4), and concentrated. Flash chromatography (gradient elution: 10-40% EtOAc in hexanes) of the crude material afforded the title compound as a clear oil. MS m/z: 416 (M+1). Calc'd for C20H18FN3O4S: 415.10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06822097B1
Source datasetuspto-grants-2004_11
ORD IDord-10339fde41cc4c6f83a37241ddc84bae
Source noteuspto-grants-2004_11