HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657002Generated: October 31, 2026
m-Chloroperbenzoic acid → 2-Amino-5-(5-trifluoromethylpyridin-2-ylsulfinyl)thiazole
https://huagongshe.com/reaction/1657002
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2-Amino-5-(5-trifluoromethylpyridin-2-ylthio)thiazole | HCID 15729200 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Amino-5-(5-trifluoromethylpyridin-2-ylsulfinyl)thiazole | HCID 15729205 | 81.9% |
Reaction Steps
To a solution of 2-amino-5-(5-trifluoromethylpyridin-2-ylthio)thiazole (0.6 g) in dichloromethane (20 ml) was added portionwise 3-chloroperbenzoic acid (0.6 g) at 5° C. with stirring. The mixture was stirred at 5° C. for 3 hours. The reaction mixture was washed with aqueous sodium bicarbonate and dried over magnesium sulfate. The solvent was concentrated under reduced pressure to give solid. The solid was subjected to column chromatography on silica gel (silica gel 60, 70-230 mesh; Merck: 30 g) and eluted with a mixture of chloroform and methanol (10:1). The fractions containing the objective compound were combined and concentrated under reduced pressure to give 2-amino-5-(5-trifluoromethylpyridin-2-ylsulfinyl)thiazole (0.52 g, yield: 81.9%). mp: 144°-145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05256675 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-faaa2f8cb7da41e4a467e7ae572ff0cb |
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| Source note | uspto-grants-1993_10 |
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