HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656990Generated: November 3, 2026
m-Chloroperbenzoic acid → 2-Amino-4-methyl-5-(2-pyridylsulfinyl)thiazole
https://huagongshe.com/reaction/1656990
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2-Amino-4-methyl-5-(2-pyridylthio)thiazole | HCID 18954735 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Amino-4-methyl-5-(2-pyridylsulfinyl)thiazole | HCID 15729189 | 52.2% |
Reaction Steps
A mixture of 2-amino-4-methyl-5-(2-pyridylthio)thiazole (1.7 g) and 3-chloroperbenzoic acid (1.8 g) in a mixture of chloroform (20 ml) and dichloromethane (50 ml) was stirred at 5° C. for 3.5 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: 100 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-4-methyl-5-(2-pyridylsulfinyl)thiazole (0.95 g, yield: 52.2 %). mp: 190°-193° C. (dec.)
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-3d40e69cefd048dc94fa9772c97cb315 |
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| Source note | uspto-grants-1993_10 |
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