HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-Amino-5-(3-pyridylsulfonyl)thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2-Amino-5-(3-pyridylsulfinyl)thiazole | HCID 15729197 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Amino-5-(3-pyridylsulfonyl)thiazole | HCID 15729198 | 17.5% |
Reaction Steps
A mixture of 2-amino-5-(3-pyridylsulfinyl)thiazole (1.6 g) and 3-chloroperbenzoic acid (1.8 g) in a mixture of chloroform (150 ml), dichloromethane (50 ml) and N,N-dimethylformamide (5 ml) was stirred at room temperature for 3 hours. The reaction mixture was extracted with diluted hydrochloric acid and washed with ethyl acetate. The aqueous layer was adjusted to pH 8.5 using sodium bicarbonate and the mixture was extracted with a mixture of tetrahydrofuran and ethyl acetate (1:1). The organic layer was washed with water and dried over magnesium sulfate. The solvent was concentrated under reduced pressure and the residue was triturated with ethanol to give 2-amino-5-(3-pyridylsulfonyl)thiazole (0.30 g, yield: 17.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05369107 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-fa4cb532e22a421a9bcf75231a8990b8 |
| Source note | uspto-grants-1994_11 |