HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914396Generated: October 30, 2026
Trifluoroacetic acid → HCID 178460790, compound
https://huagongshe.com/reaction/914396
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | {2-[(2-Tert-butoxy-1,1-dimethyl-2-oxoethyl)thio]-1,3-thiazol-4-yl}acetic acid | HCID 59759443 | — |
| Reactant | HCID 178507284 | HCID 178507284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178460790 | HCID 178460790 | — |
Reaction Steps
The compound obtained using {2-[(2-tert-butoxy-1,1-dimethyl-2-oxoethyl)thio]-1,3-thiazol-4-yl}acetic acid synthesized in Example 3 and 3-(4-chlorophenyl)-1H-pyrazole-5-amine as starting materials and by operations similar to those of Example 242-1 and Example 242-2 was treated with dichloromethane and trifluoroacetic acid, and the mixture was stirred at room temperature for 12 hr. The reaction mixture was concentrated under reduced pressure, ethyl acetate was added, and the mixture was washed with saturated aqueous sodium hydrogen carbonate solution (The objective compound was extracted in the saturated aqueous sodium hydrogen carbonate solution layer). Aqueous 10% citric acid solution was added to the aqueous layer, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08026370B2 |
|---|
| Source dataset | uspto-grants-2011_09 |
|---|
| ORD ID | ord-0a11d4c4ab5745bfb7e811b5b1fd0ca7 |
|---|
| Source note | uspto-grants-2011_09 |
|---|