HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715741Generated: October 30, 2026
4-Bromophenacyl bromide → HCID 1130426, compound
https://huagongshe.com/reaction/715741
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromophenacyl bromide | HCID 7454 | — |
| Reactant | Prothionamide | HCID 666418 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 1130426 | HCID 1130426 | 79.6% |
Reaction Steps
As shown in FIG. 27, in reaction (a) a mixture of prothionamide (9.01 g, 50.0 mmol) and 4-bromophenacyl bromide 6a (13.9 g, 50.0 mmol) in EtOH (400 mL) was stirred at 70° C. for 1 h. After cooled to room temperature, the precipitation was filtered off with EtOAc and washed with EtOAc and saturated aqueous NaHCO3. The organic layer was washed with brine, dried over Na2SO4, and concentrated to give 4-(4-bromophenyl)-2-(2-propylpyridin-4-yl)thiazole 2 (14.3 g, 79%) as a light-yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187485B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-25f6d0e6175d4f8fa4ab8b83f527d95f |
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| Source note | uspto-grants-2015_11 |
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