HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596087Generated: October 29, 2026
Sodium Carbonate → Methyl 4-(3-aminopyrazin-2-yl)-2-fluorobenzoate
https://huagongshe.com/reaction/596087
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Amino-3-chloropyrazine | HCID 276224 | — |
| Reactant | 3-Fluoro-4-methoxycarbonylphenylboronic acid, pinacol ester | HCID 22171528 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Methyl 4-(3-aminopyrazin-2-yl)-2-fluorobenzoate | HCID 118045820 | 111.1% |
Reaction Steps
To a mixture of 3-chloropyrazin-2-amine (5 g, 38.6 mmol) in DME (160 mL) and aq. 2 M sodium carbonate (40 mL, 80 mmol) was added methyl 2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (12.97 g, 46.3 mmol) followed by PdCl2(dppf)-CH2Cl2 adduct (3.15 g, 3.86 mmol). The reaction mixture was purged with N2 and heated in an oil bath at 100° C. for 3-4 h. The reaction mixture was partitioned between ethylacetate and water. The organic layer was separated, washed with brine, dried over sodium sulfate, filtered and evaporated. The crude was triturated with DCM. Solid observed was filtered, washed with ether and dried under reduced pressure to provide product as an off white solid. Filtrate was purified by flash chromatography eluting with 0-50-80% EtOAc/heptane to provide 10.6 g of product in 93% yield. LCMS (m/z): 248.1 (MH+), 0.563 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242996B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-80f8d6ffad4f497d9efd08d49c5d3705 |
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| Source note | uspto-grants-2016_01 |
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