HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 4-amino-2-(methylsulfonyl)thiazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Methyl 4-amino-2-(methylsulfanyl)-1,3-thiazole-5-carboxylate | HCID 609212 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 4-amino-2-(methylsulfonyl)thiazole-5-carboxylate | HCID 59511825 | — |
Reaction Steps
After adding 45.2 g of 4-amino-2-methylsulfanylthiazole-5-carboxylic acid methyl ester [CAS No. 60093-05-2] to 2 liters of a water:methanol=1:1 mixed solvent at room temperature, 408 g of Oxone was added in small portions over a period of 30 minutes with stirring. The mixture was stirred at room temperature for 24 hours, and then poured into a mixture of 10 liters of ethyl acetate and 10 liters of water. After washing the organic layer with 5 liters of saturated brine, it was dried over anhydrous magnesium sulfate. The desiccating agent was filtered off, and the filtrate was concentrated under reduced pressure to give the title compound (37.6 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07816522B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-f8868a0534fa4200ad72ce3db3b9ac99 |
| Source note | uspto-grants-2010_10 |