HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908193Generated: October 31, 2026
Bromine → [5-(4-Methanesulfonyl-3-trifluoromethyl-phenyl)-4-methyl-thiazol-2-yl]-pyrazin-2-yl-amine
https://huagongshe.com/reaction/908193
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | N-Pyrazinylthiourea | HCID 2771013 | — |
| Reactant | 1-(4-Methanesulfonyl-3-trifluoromethyl-phenyl)-propan-2-one | HCID 67391018 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | [5-(4-Methanesulfonyl-3-trifluoromethyl-phenyl)-4-methyl-thiazol-2-yl]-pyrazin-2-yl-amine | HCID 86606223 | — |
Reaction Steps
1-(4-Methanesulfonyl-3-trifluoromethyl-phenyl)-propan-2-one (Example 59c) (0.60 g, 2.14 mmol) is dissolved in dioxan (50 ml) and the solution is cooled to 10° C. at which point the mixture is semi frozen. Bromine (0.088 ml, 1.7 mmol) is added slowly and the mixture is stirred for an additional 30 min in a semi frozen state. The mixture is then allowed to warm to room temperature and the solvent is removed to give a brown oil. This material is dissolved in ethanol and pyrazin-2-yl-thiourea (1a) is added in one portion. The mixture is stirred at 60° C. for 30 minutes then allowed to cool whereupon the titled product precipitates and is removed by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017608B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-ddff63fc334c420fb96dcb2389279267 |
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| Source note | uspto-grants-2011_09 |
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