HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257384Generated: November 1, 2026
2-Oxobutanoic Acid → Methyl 2-amino-5-methyl-1,3-thiazole-4-carboxylate
https://huagongshe.com/reaction/1257384
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Oxobutanoic Acid | HCID 58 | — |
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl 2-amino-5-methyl-1,3-thiazole-4-carboxylate | HCID 1132801 | 23% |
Reaction Steps
Under a nitrogen atmosphere at 0° C., to a solution of 2-oxobutyric acid (12 g, 120 mmol) in methanol was added thionyl chloride (40 mL, 330 mmol), and the mixture was stirred at the same temperature for 3 hr. The solvent was evaporated under reduced pressure. Under a nitrogen atmosphere at 0° C., to a solution (50 mL) of the residue in diethyl ether was slowly added dropwise a solution (50 mL) of bromine (10 g, 130 mmol) in diethyl ether, and the mixture was stirred overnight while allowing the mixture to spontaneously warm. The solvent was evaporated under reduced pressure. An aqueous solution (120 mL) of the residue and thiourea (6.3 g, 83 mmol) was heated under reflux for 3 hr, and cooled to room temperature. The reaction mixture was neutralized with 20% aqueous ammonia solution. The resulting crude title compound was collected by filtration, washed with water to give the title compound (3.3 g, 23%) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461348B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-105b28fe59eb47fcab998e5043e04d93 |
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| Source note | uspto-grants-2013_06 |
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