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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076191Generated: October 30, 2026

Iodine chloride → 3-(2-Fluoro-4-iodo-phenylamino)-5-formylaminomethyl-pyrazine-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/2076191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodine chlorideHCID 24640—
ReactantHCID 59140179HCID 59140179—
SolventDichloromethaneHCID 6344—
Product3-(2-Fluoro-4-iodo-phenylamino)-5-formylaminomethyl-pyrazine-2-carboxylic acid methyl esterHCID 5914013999%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold (0° C.) solution of 3-(2-fluoro-4-trimethylsilanyl-phenylamino)-5-formylaminomethyl-pyrazine-2-carboxylic acid methyl ester (480 mg, 1.28 mmol) in dichloromethane (13 mL) under N2 was added dropwise a solution of 1M iodine monochloride in dichloromethane (3.0 mL, 3.0 mmol, 2.4 eq), and the mixture was stirred at 0° C. for 1.5 hour. The reaction was quenched by addition of a saturated aqueous solution of sodium thiosulfate (3 mL). After stirring for 10 minutes the reaction mixture was poured into ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium bicarbonate, water and brine, dried (Na2SO4), filtered and evaporated in vacuo to afford the desired product as a yellow solid (548 mg, 99%). LCMS (method C): RT=2.65 min, [M+H]+=431.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923456B2
Source datasetuspto-grants-2011_04
ORD IDord-4769eec31504481ab033884dc728e070
Source noteuspto-grants-2011_04