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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264899Generated: October 30, 2026

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

https://huagongshe.com/reaction/2264899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodine chlorideHCID 24640—
Reactant3-(2-Fluoro-4-trimethylsilanyl-phenylamino)-1-methyl-1H-pyrrolo[3,2-c]pyridine-2-carboxylic acid ethyl esterHCID 59596497—
SolventDichloromethaneHCID 6344—
Product3-(2-Fluoro-4-iodo-phenylamino)-1-methyl-1H-pyrrolo[3,2-c]pyridine-2-carboxylic acid ethyl esterHCID 5959658752%

Reaction Steps

A solution of 3-(2-fluoro-4-trimethylsilanyl-phenylamino)-1-methyl-1H-pyrrolo[3,2-c]pyridine-2-carboxylic acid ethyl ester (37.0 g, 96.0 mmol) in CH2Cl2 (500 mL) was cooled to 0-5° C. and treated dropwise with iodine monochloride solution (211 mL, 1M in CH2Cl2). The mixture was allowed to warm and stirring continued for 1 hour. The solution was washed with aqueous sodium thiosulfate solution, dried (MgSO4) and evaporated in vacuo. The resultant residue was triturated with ethyl acetate to give the title compound (21.8 g, 52%) as a yellow solid. LCMS (method B): RT=2.48 min, M+H+=440.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855216B2
Source datasetuspto-grants-2010_12
ORD IDord-4f9683a1d6f44084b94d4d6b6ecbc133
Source noteuspto-grants-2010_12