HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-[Methyl(methylsulfonyl)amino]-1,3-oxazole-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl 2-[methyl(methylsulfonyl)amino]-1,3-oxazole-4-carboxylate | HCID 21086092 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[Methyl(methylsulfonyl)amino]-1,3-oxazole-4-carboxylic acid | HCID 21085471 | 82.4% |
Reaction Steps
To a 50 ml round bottom flask was added (61 mg, 0.2457 mmoles) ethyl 2-[methyl(methylsulfonyl)amino]-1,3-oxazole-4-carboxylate, (51.5 mg, 1.2274 mmoles, 5.0 eq.) lithium hydroxide, (2.5 ml) tetrahydrofuran and (1.5 ml) water. The reaction was agitated at ambient temperature for ˜2 hours. The reaction was complete by electrospray mass spec. The reaction was worked up by adding (5 ml) 1N HCl and then extracting with ethyl acetate. The organic layer was washed with water and brine and then dried with magnesium sulfate. The solution was then evaporated to dryness, leaving (44.6 mg) of 2-[methyl(methylsulfonyl)amino]-1,3-oxazole-4-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07727997B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-eb200b5b9a7246ccbd53a3d7b0c0fb9a |
| Source note | uspto-grants-2010_06 |