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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588412Generated: October 30, 2026

N-Iodosuccinimide → 3-iodo-2-methyl-1H-pyrrolo[2,3-c]pyridine

https://huagongshe.com/reaction/588412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant2-Methyl-1H-pyrrolo(2,3-c)pyridineHCID 12407505—
SolventChloroformHCID 6212—
Product3-iodo-2-methyl-1H-pyrrolo[2,3-c]pyridineHCID 6741851292%

Reaction Steps

2-Methyl-1H-pyrrolo[2,3-c]pyridine (100 mg, 0.76 mmol) was dissolved in CHCl3 (5 mL), N-iodosuccinimide (179 mg, 0.79 mmol) was added and the reaction mixture was stirred for 2 h. The reaction mixture was quenched with 1 M aq sodium thiosulphate (5 mL) and the CHCl3 was removed in vacuo. The reaction mixture was partitioned between sat aq NaHCO3 (40 mL) and EtOAc (40 mL). The aqueous layer was extracted with EtOAc (40 mL) and the combined organic fractions were washed with sat aq NaHCO3 (50 mL) and brine (50 mL), dried (MgSO4) and concentrated in vacuo to give the title compound as a cream solid (179 mg, 92%). LCMS (ES+): 258.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227967B2
Source datasetuspto-grants-2016_01
ORD IDord-0bc03b6cdbca44099e42bb0342e9bb07
Source noteuspto-grants-2016_01