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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171136Generated: October 25, 2026

Citric Acid → 3-Amino-6-iodopyrazine-2-carboxylic acid

https://huagongshe.com/reaction/1171136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantLithium HydroxideHCID 3939—
ReactantMethyl 3-amino-6-iodopyrazine-2-carboxylateHCID 11087124—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product3-Amino-6-iodopyrazine-2-carboxylic acidHCID 4683560287%

Reaction Steps

3-amino-6-iodo-pyrazine-2-carboxylic acid methyl ester (45 g, 161 mmol) was dissolved in 750 ml of THF. 90 ml of water and 40 ml of a 4 M solution of lithium hydroxide in water was added. The mixture was stirred at room temperature for 2 hours or until TLC analysis showed only baseline material. A solution of 10% citric acid in water was added to adjust the pH to about 3-4. The mixture was diluted with dichloromethane and the organic phase was separated. The aqueous layer was extracted three times with dichloromethane and the combined organic phases were dried over sodium sulfate and evaporated. The residue was dried in vacuo to afford 37.0 g (140 mmol; 87% yield) of 3-amino-6-iodo-pyrazine-2-carboxylic acid as a yellow powder. 1H-NMR (d6-DMSO) δ: 11.70 s, weak, 8.44 [1H] s, 7.50 [2H] s, br. MS: m/z 266 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829558B2
Source datasetuspto-grants-2010_11
ORD IDord-c394f2eeb88e4ed5a40c3b74c1b31452
Source noteuspto-grants-2010_11