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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40870Generated: October 29, 2026

Bromine → 3-Bromo-5-methyl-1-tosyl-1h-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/40870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant1H-Pyrrolo[2,3-B]pyridine, 5-methyl-1-[(4-methylphenyl)sulfonyl]-HCID 49758924—
SolventDichloromethaneHCID 6344—
Product3-Bromo-5-methyl-1-tosyl-1h-pyrrolo[2,3-b]pyridineHCID 4975897999%

Reaction Steps

5-methyl-1-tosyl-1H-pyrrolo[2,3-b]pyridine (1.9 g, 6.62 mmol) in dichloromethane (40 mL) was treated dropwise with a solution of bromine (0.678 mL, 13.24 mmol) in dichloromethane (3 mL). The resulting solution was stirred at room temperature for 3 hours. The reaction mixture was partitioned between dichloromethane (150 mL) and a 1:1 mixture of a saturated aqueous solution of NaHCO3 and a saturated aqueous solution of Na2S2O3 (250 mL). The organic phase was separated and the aqueous phase was re-extracted twice with DCM (50 mL). The combined organic phases were dried over magnesium sulfate and concentrated in vacuo to give the desired compound as an off-white solid (2.381 g, 99% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530489B2
Source datasetuspto-grants-2013_09
ORD IDord-0d04107c40074aedadb2a7cc25d12507
Source noteuspto-grants-2013_09