HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830771Generated: November 1, 2026
Cesium carbonate → 3-Bromo-5-phenylpyrazin-2-amine
https://huagongshe.com/reaction/1830771
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 2-Amino-3,5-dibromopyrazine | HCID 620004 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Bromo-5-phenylpyrazin-2-amine | HCID 12453552 | 88% |
Reaction Steps
To a stirred solution of 3,5-dibromo-2-aminopyrazine (200 mg; 0.79 mmol) and phenyl boronic acid (106 mg; 0.87 mmol) in dioxane (4 mL) and ethanol (2 mL) was added cesium carbonate (571 mg; 1.75 mmol in 2 mL of water) followed by Pd(PPh3)4 (46 mg; 0.04 mmol). The reaction was heated to 75° C. and stirred for 12 hours. The reaction was cooled to room temperature, diluted with 50 mL of ethyl acetate and washed with aqueous 10% sodium carbonate (1×50 mL), brine (50 mL), then dried (MgSO4), and filtered. The material was purified using a biotage 12L cartridge eluting with hexanes and ethyl acetate (3:1) to yield an off white solid (88% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07067506B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-20b9c31469d645ce8e326d11f026082a |
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| Source note | uspto-grants-2006_06 |
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