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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416470Generated: October 30, 2026

Isoamyl Nitrite → 5-Bromo-6-(4-chloro-phenyl)-3-trifluoromethyl-pyrazine-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/416470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl NitriteHCID 8053—
ReactantBromotrimethylsilaneHCID 76113—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Amino-6-(4-chloro-phenyl)-3-trifluoromethyl-pyrazine-2-carboxylic acid methyl esterHCID 66622595—
SolventDibromomethaneHCID 3024—
Product5-Bromo-6-(4-chloro-phenyl)-3-trifluoromethyl-pyrazine-2-carboxylic acid methyl esterHCID 8663470291%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 2.11 g 5-amino-6-(4-chloro-phenyl)-3-trifluoromethyl-pyrazine-2-carboxylic acid methyl ester in 20 ml dibromomethane was added 1.59 g isoamylnitrite and the mixture was cooled to 0° C. To the resulting suspension was added 2.922 g trimethylbromosilane and the mixture was stirred at 0° C. for 10 min (no conversion by HPLC) and at room temperature for 3 h. To the dark reaction mixture was added another 1.59 g isoamylnitrite and the mixture was stirred at room temperature for 6 h. The dark reaction mixture was pored onto ice and ca 20 ml 10% sodium bicarbonate and the product was extracted with dichloromethane (2.64 g raw material which crystallized) and purified by chromatography on silica gel (20 g hep:EE=9:1 to 1:1) to yield 2.290 g of the title compound as white crystals. MS (M+H at 396.8 and 394.9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088920B2
Source datasetuspto-grants-2012_01
ORD IDord-0a8c97580b204972bd1e313ca2a6edab
Source noteuspto-grants-2012_01