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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901357Generated: October 30, 2026

N-Iodosuccinimide → 5-Bromo-3-iodo-1H-pyrrolo(2,3-b)pyridine

https://huagongshe.com/reaction/901357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant5-bromo-1H-pyrrolo[2,3-b]pyridineHCID 10307932—
SolventAcetoneHCID 180—
Product5-Bromo-3-iodo-1H-pyrrolo(2,3-b)pyridineHCID 2422921274%

Reaction Steps

Into a 500 mL round bottomed flask were added 5-bromo-1H-pyrrolo[2,3-b]pyridine (10.11 g, 51.3 mmol) and 250 ml acetone. N-iodosuccinimide (NIS, 12.7 g, 56.4 mmol) was added, and the reaction mixture was stirred at room temperature for 1 hour. The precipitate was collected and washed with cold acetone to afford 12.2 g (74%) of the title compound as a tan powder. 1H-NMR (500 MHz, d6-DMSO) δ=12.35 (br.s, 1H), 8.29 (d, J=2.0 Hz, 1H), 7.84 (d, J=2.0 Hz 1H), 7.79 (s, 1H); MS: m/z 322.8/324.8 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361763B2
Source datasetuspto-grants-2008_04
ORD IDord-91694d5ddeb44220a311f325f49a298a
Source noteuspto-grants-2008_04