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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929933Generated: October 30, 2026

Isoamyl Nitrite → 5-Bromo-6-(4-fluoro-phenyl)-pyrazine-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1929933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl NitriteHCID 8053—
ReactantBromotrimethylsilaneHCID 76113—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Amino-6-(4-fluoro-phenyl)-pyrazine-2-carboxylic acid methyl esterHCID 67504641—
SolventDibromomethaneHCID 3024—
Product5-Bromo-6-(4-fluoro-phenyl)-pyrazine-2-carboxylic acid methyl esterHCID 86616957—

Reaction Steps

To a suspension of 5-amino-6-(4-fluoro-phenyl)-pyrazine-2-carboxylic acid methyl ester (1.26 g, 5.10 mmol, 1.0 eq) in dibromomethane (25 ml) was added isoamyl nitrite (0.85 ml, 6.29 mmol, 1.2 eq) at room temperature. The resulting suspension was added over 30 minutes at room temperature to a dibromomethane (5 ml) solution of trimethylbromosilane (0.82 ml, 5.90 mmol, 1.15 eq). The mixture was stirred for 2 hours at room temperature after which time the turbid solution was added to aqueous sodium bicarbonate (10%, 15 ml). The phases were mixed, separated and the organic layer dried over magnesium sulfate, concentrated in vacuo and purified by chromatography on silica gel using a gradient of heptane to 10% ethyl acetate in heptane to afford 5-Bromo-6-(4-fluoro-phenyl)-pyrazine-2-carboxylic acid methyl ester as white crystals. Yield=0.81 g (51%). 1H NMR (250 MHz, DMSO): δ 3.92 (3H, s), 7.38 (2H, t, J=8.98 Hz), 7.76-7.81 (2H, m), 8.98 (1H, s). HPLC-MS=100%; 2.13 min (MW=311; M+1=313.0).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188093B2
Source datasetuspto-grants-2012_05
ORD IDord-1a4ebfc6243a47288927a2a96e31a2ca
Source noteuspto-grants-2012_05