HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092957Generated: October 26, 2026
Water → N-[5-(4-Fluoro-3-methanesulfonyl-phenyl)-4-methyl-thiazol-2-yl]-acetamide
https://huagongshe.com/reaction/1092957
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Acetylthiourea | HCID 2723593 | — |
| Reactant | 1-Bromo-1-(4-fluoro-3-methanesulfonyl-phenyl)-propan-2-one | HCID 85861733 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[5-(4-Fluoro-3-methanesulfonyl-phenyl)-4-methyl-thiazol-2-yl]-acetamide | HCID 86598409 | — |
Reaction Steps
A mixture of 1-bromo-1-(4-fluoro-3-methanesulfonyl-phenyl)-propan-2-one (Example 47c) (0.17 g, 0.55 mmol) and N-acetylthiourea (0.065 g, 0.55 mmol) in ethanol is heated at 70° C. for 3 hours then at room temperature over two days. The reaction mixture is poured into water (200 ml) and extracted with ethyl acetate (3×50 ml). The combined organic layers are dried over MgSO4, filtered and concentrated to afford a viscous solid. This solid in a minimum amount of ethyl acetate is sonicated to give a suspension which is then heated until all solid has dissolved then left to cool to room temperature overnight. The white crystalline solid is filtered off to afford the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08129541B2 |
|---|
| Source dataset | uspto-grants-2012_03 |
|---|
| ORD ID | ord-d17b137964724b859eba21680c2997fc |
|---|
| Source note | uspto-grants-2012_03 |
|---|