HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499190Generated: November 1, 2026
Cesium carbonate → (R)-4-(1-(2-bromo-4-chlorophenyl)-2,2,2-trifluoroethoxy)-6-chloropyrimidin-2-amine
https://huagongshe.com/reaction/1499190
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Amino-4,6-dichloropyrimidine | HCID 65522 | — |
| Reactant | (R)-1-(2-bromo-4-chlorophenyl)-2,2,2-trifluoroethanol | HCID 66742830 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (R)-4-(1-(2-bromo-4-chlorophenyl)-2,2,2-trifluoroethoxy)-6-chloropyrimidin-2-amine | HCID 117942233 | — |
Reaction Steps
To a solution of (R)-1-(2-bromo-4-chlorophenyl)-2,2,2-trifluoroethanol (Intermediate 43) (400 mg, 1.4 mmol) in dioxane (25 mL) was added 4,6-dichloropyrimidin-2-amine (1.1 g, 7 mmol) and Cs2CO3 (1.3 g, 4 mmol). The mixture was heated for 24 h at 80° C. The reaction was then cooled to RT and filtered. The solvent was removed in vacuo, then CH2Cl2 and heptane was added. The solvent volume was reduced until a solid precipitated out. The solid was filtered and the procedure repeated several times to provide (R)-4-(1-(2-bromo-4-chlorophenyl)-2,2,2-trifluoroethoxy)-6-chloropyrimidin-2-amine as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199994B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-0fa8eb0d6cee4610bbc788972df3ba1d |
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| Source note | uspto-grants-2015_12 |
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