HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171513Generated: October 29, 2026
Methanol → Methyl 4-amino-2-(methylsulfonyl)thiazole-5-carboxylate
https://huagongshe.com/reaction/2171513
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 | — |
| Product | Methyl 4-amino-2-(methylsulfonyl)thiazole-5-carboxylate | HCID 59511825 | — |
Reaction Steps
5.12 g (8.32 mmol) of Oxone® are dissolved in 170 ml of water and cooled to 5° C. A solution of 1 g (4.90 mmol) of methyl 4-amino-2-(methylsulphanyl)-1,3-thiazole-5-carboxylate in 18 ml of methanol is then added dropwise, and the solution is stirred at RT for 3 h. The major amount of methanol is removed and extracted three times with dichloromethane. The combined organic phases are dried with sodium sulphate. After removal of the solvent and drying of the residue under high vacuum, the resulting solid (824 mg (43% of theory)) is employed without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051323B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-abe1c416d5d84f9bac9122c336f5bad7 |
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| Source note | uspto-grants-2015_06 |
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