HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359151Generated: October 30, 2026
Lithium Hexamethyldisilazide → 1-(4-(4-Bromo-3,5-dimethoxyphenyl)thiazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)ethanone
https://huagongshe.com/reaction/2359151
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | N,2-dimethoxy-N-methyl-2-(4-morpholinophenyl)acetamide | HCID 58431993 | — |
| Reactant | 4-(4-Bromo-3,5-dimethoxyphenyl)thiazole | HCID 58432046 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-(4-Bromo-3,5-dimethoxyphenyl)thiazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)ethanone | HCID 58432081 | 29.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08685975B2 |
|---|
| Source dataset | uspto-grants-2014_04 |
|---|
| ORD ID | ord-4bf46b917737489cba8ae84a4287ff98 |
|---|
| Source note | uspto-grants-2014_04 |
|---|