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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331010Generated: October 30, 2026

N-Iodosuccinimide → 4-bromo-3-iodo-2-methyl-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/331010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant4-Bromo-2-methyl-1H-pyrrolo(2,3-b)pyridineHCID 52987786—
SolventDichloromethaneHCID 6344—
Product4-bromo-3-iodo-2-methyl-1H-pyrrolo[2,3-b]pyridineHCID 7109019393%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 4-bromo-2-methyl-1H-pyrrolo[2,3-b]pyridine (D24) (1.65 g, 7.82 mmol) in DCM (70 mL) was added NIS (1.935 g, 8.60 mmol) at 0° C. and the mixture was stirred for 1.5 hour at 0° C. The mixture was evaporated in vacuo. DCM (ca. 20 mL) was added to the residue. The formed precipitate was filtered, rinsed with DCM to give the title compound (2.45 g). LCMS (A): m/z (M+H)+ 337/339, C8H6BrIN2 requires 336/338 (acidic).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877742B2
Source datasetuspto-grants-2014_11
ORD IDord-864ac5436dfa4d54a94e5208c668edf3
Source noteuspto-grants-2014_11