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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646778Generated: November 1, 2026

1,3-Benzenedicarboxylic acid, 5-bromo-, 1,3-dimethyl ester → HCID 86607854, compound

https://huagongshe.com/reaction/646778

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Benzenedicarboxylic acid, 5-bromo-, 1,3-dimethyl esterHCID 103954—
ReactantMethyl 3-Amino-6-bromopyrazine-2-carboxylateHCID 227251—
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium AcetateHCID 517044—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86607854HCID 8660785412%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture containing 5-bromoisophthalic acid dimethyl ester (0.20 g, 0.73 mmol), bispinacolatodiboron (0.21 g, 0.80 mmol), 1,1′-bis(diphenylphosphine)ferrocene palladium dichloride (0.029 g, 0.035 mmol), and potassium acetate (0.26 g, 2.3 mmol) in dioxane (5 mL) was heated at 80° C. for 1 h. The reaction mixture was cooled to room temperature and methyl 3-amino-6-bromo-pyrazine-2-carboxylate (0.17 mg, 0.70 mmol), 1,1′-bis(diphenylphosphine)ferrocene palladium dichloride (0.035 g, 0.042 mmol), sodium bicarbonate (320 mg, 3.8 mmol), and water (1 mL) were added. The mixture was heated at 80° C. for 12 h, after which time, the mixture was diluted with water and ethyl acetate. The layers were separated and the organic layer was extracted with 1 N hydrochloric acid (2×) and dried over sodium sulfate. Filtration, concentration, and silica gel chromatography gave the product as a yellow solid (23 mg, 12% yield). 1H NMR (400 MHz, d6-DMSO): δ 9.04 (s, 1H), 8.74 (d, 2H), 8.44 (t, 1H), 7.62 (s, 2H), 3.32 (s, 3H), 2.49 (s, 3H), 2.48 (s, 3H). MS (EI) for C16H15N3O6: 346 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07704995B2
Source datasetuspto-grants-2010_04
ORD IDord-7685ce800bad4510b29c681755c3da5b
Source noteuspto-grants-2010_04