HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799694Generated: October 30, 2026
Ammonia → 4-Bromo-1,3-thiazole-2-carboxamide
https://huagongshe.com/reaction/1799694
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4-Bromo-1,3-thiazole-2-carboxylic acid | HCID 15122065 | — |
| Reactant | Tetrahydrofurane dichloromethane | HCID 21919333 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 4-Bromo-1,3-thiazole-2-carboxamide | HCID 59238466 | — |
Reaction Steps
Oxalyl dichloride (1.61 ml) was added to 100 ml of a mixed solution composed of 4-bromo-2-carboxythiazole and THF-dichloromethane (2:1), and the mixture was stirred at 60° C. for 2 hr. Under ice cooling, 15 ml of 30% aqueous ammonia was added to the reaction solution, and the mixture was stirred at the same temperature for 30 min. Ethyl acetate (50 ml) and 50 ml of semi-saturated brine were added thereto, followed by separation. The organic layer was then dried over anhydrous magnesium sulfate, the solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography on silica gel (chloroform:methanol=40:1) to give 1.36 g of 4-bromo-2-carbamoylthiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344154B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-8a85dacda6084572bc555b00555691b5 |
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| Source note | uspto-grants-2013_01 |
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