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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56492Generated: 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/56492

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 numberUS09434707B2
Source datasetuspto-grants-2016_09
ORD IDord-b5597a786de747bda48989824f1bba6b
Source noteuspto-grants-2016_09