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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512591Generated: October 29, 2026

Lithium Hexamethyldisilazide → 1-(4-(4-Bromo-3,5-dimethoxyphenyl)thiazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)ethanone

https://huagongshe.com/reaction/512591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantN,2-dimethoxy-N-methyl-2-(4-morpholinophenyl)acetamideHCID 58431993—
Reactant4-(4-Bromo-3,5-dimethoxyphenyl)thiazoleHCID 58432046—
SolventTetrahydrofuranHCID 8028—
Product1-(4-(4-Bromo-3,5-dimethoxyphenyl)thiazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)ethanoneHCID 5843208129.3%

Reaction Steps

To a −78° C. solution of 4-(4-bromo-3,5-dimethoxyphenyl)thiazole (0.096 g, 0.32 mmol) in anhydrous THF (2 mL) under argon was added a solution of LiHMDS (1.0 M in THF, 0.35 mmol) dropwise. After stirring for 30 min, a solution of N, 2-dimethoxy-N-methyl-2-(4-morpholinophenyl)acetamide (0.121 g, 0.41 mmol) in anhydrous THF (1.5 mL, 1.0 mL) was added dropwise. After stirring for 35 min, the cold bath was removed and the reaction was allowed to warm to room temp. The mixture was quenched with brine and diluted with EtOAc. The layers were separated and the organic layer was washed with brine, dried over Na2SO4 and concentrated. Purification by chromatography (25-45% EtOAc-hexanes) gave 1-(4-(4-bromo-3,5-dimethoxyphenyl)thiazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)ethanone as a yellow solid (0.050 g, 29% yield). MS: m/z 533.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102643B2
Source datasetuspto-grants-2015_08
ORD IDord-48ef0b679e704b00bf44d5bf533757cb
Source noteuspto-grants-2015_08