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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272056Generated: October 26, 2026

Citric Acid → (3-Amino-6-iodo-pyrazin-2-yl)-phenyl-methanone

https://huagongshe.com/reaction/272056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
Reactant3-Amino-6-iodo-pyrazine-2-carboxylic acid methoxy-methyl-amideHCID 59836115—
ReactantHCID 178418255HCID 178418255—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product(3-Amino-6-iodo-pyrazin-2-yl)-phenyl-methanoneHCID 5983611468%

Reaction Conditions

Temperature55 °C

Reaction Steps

8.00 g (25.97 mmol) of 3-amino-6-iodo-pyrazine-2-carboxylic acid methoxy-methyl-amide was dissolved in 100 ml of anhydrous THF under nitrogen. The solution was cooled to 55° C. and 27 ml of a 3 M solution of phenylmagnesium bromide in ether was added. The mixture was allowed to warm to 10° C. and a solution of 10% citric acid in water was added. The mixture was diluted with dichloromethane and the phases were separated. The aqueous phase was extracted three times with dichloromethane and the combined organic phases were dried over sodium sulfate and evaporated. The resulting solid was crystallized from ethanol to afford 5.74 g (17.66 mmol; 68%) of (3-amino-6-iodo-pyrazin-2-yl)-phenyl-methanone as yellow-orange crystals. 1H-NMR (d6-DMSO) δ: 8.52 [1H] s, 7.94 [2H] s,br, 7.85 [2H] d, 7.62 [1H] t, 7.52 [2H] t. MS: m/z 326 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452993B2
Source datasetuspto-grants-2008_11
ORD IDord-156e8396442d4655808ff938c142d10f
Source noteuspto-grants-2008_11