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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272244Generated: October 30, 2026

Ethyl Acetate → 5-(2-Fluoro-6-methylbenzo[b]furan-5-yl)-pyrazine-2-ylamine

https://huagongshe.com/reaction/2272244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazin-2-amineHCID 17998987—
Reactant5-Bromo-2-fluoro-6-methyl-benzofuranHCID 58487394—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Solvent1,4-DioxaneHCID 31275—
Product5-(2-Fluoro-6-methylbenzo[b]furan-5-yl)-pyrazine-2-ylamineHCID 5848684525.4%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 5-bromo-2-fluoro-6-methyl-benzofuran (230) (0.3 mmol), 2-aminopyrazine-5-boronic acid pinacol ester (133 mg, 2 eq), bis(ditertbutyl(4-dimethylaminophenyl)phosphine)dichloropalladium (II) (42 mg, 10% mol) and K3PO4 (127 mg, 0.6 mmol) in 1 ml ACN, 1 ml dioxane, 0.5 ml H2O was bubbled with argon before heated at 85° C. for 2 h. After cooling down to r.t., the reaction mixture was taken up in EA, washed with aq. NaHCO3 and brine. Org. phase was dried over Na2SO4, concentrated and then subjected to silica gel flash column chromatography (0-100% B, A: hexane; B: EA) to give 5-(2-fluoro-6-methylbenzo[b]furan-5-yl)-pyrazine-2-ylamine (234) (18.5 mg, purity>95%, yield: 25.4%) as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120751B2
Source datasetuspto-grants-2015_09
ORD IDord-a0158aba58c44ad38075260ca672590c
Source noteuspto-grants-2015_09