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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264937Generated: October 31, 2026

Iodine chloride → 7-Fluoro-3-(2-fluoro-4-iodo-phenylamino)-1H-pyrrolo[3,2-c]pyridine-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2264937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodine chlorideHCID 24640—
Reactant7-Fluoro-3-(2-fluoro-4-trimethylsilanyl-phenylamino)-1H-pyrrolo[3,2-c]pyridine-2-carboxylic acid ethyl esterHCID 59596472—
SolventDichloromethaneHCID 6344—
Product7-Fluoro-3-(2-fluoro-4-iodo-phenylamino)-1H-pyrrolo[3,2-c]pyridine-2-carboxylic acid ethyl esterHCID 5959659338%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

A solution of 7-fluoro-3-(2-fluoro-4-trimethylsilanyl-phenylamino)-1H-pyrrolo[3,2-c]pyridine-2-carboxylic acid ethyl ester (500 mg, 1.28 mmol) in CH2Cl2 (15 mL) was cooled to 0-5° C. and treated dropwise with iodine monochloride solution (2.6 mL, 1M in CH2Cl2). The mixture was stirred at 0-5° C. for one hour and then quenched by addition of a saturated aqueous sodium thiosulfate solution (10 mL). The mixture was diluted with water and dichloromethane. The precipitate formed was filtered off, washed with diethyl ether and dried under vacuum at 50° C. to give the title compound as a yellow solid (218 mg, 38%). LCMS (method B): RT=2.87 min, M+H+= 444.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855216B2
Source datasetuspto-grants-2010_12
ORD IDord-ebe984b0cdaa4b0aa12744c3ae55bb48
Source noteuspto-grants-2010_12