HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227236Generated: October 30, 2026
Ethyl bromopyruvate → 4-Methyl-2-nitro-phenyl-thiazole-4-carboxylic acid ethyl ester
https://huagongshe.com/reaction/227236
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | 4-Methyl-2-nitro-thiobenzamide | HCID 54168808 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Methyl-2-nitro-phenyl-thiazole-4-carboxylic acid ethyl ester | HCID 86622912 | — |
Reaction Steps
4-Methyl-2-nitro-thio benzamide (60 mgs, 0.30 mmol, prepared as described in compound 5, Step 2, was stirred in 1 mL absolute EtOH at room temperature under N2. Ethyl bromo pyruvate (65 mgs, 0.33 mmol) was added, and the resulting solution was heated to 70° C. for 3 h. The reaction was diluted to 30 mL with EtOAc and washed with saturated NaHCO3, and saturated NaCl. The organic layer was dried over MgSO4, filtered and concentrated to a yellow oil, which was used as is in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560462B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-0071cf80c814424a9604bf2d5f427a1a |
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| Source note | uspto-grants-2009_07 |
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