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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696202Generated: November 1, 2026

Methanesulfonyl chloride → 4-Chloro-3-nitro-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1696202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 178526747HCID 178526747—
ReactantHCID 178526852HCID 178526852—
SolventDimethylformamideHCID 6228—
Product4-Chloro-3-nitro-1H-pyrrolo[2,3-b]pyridineHCID 24729569—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of a 2:1 mixture (589.8 mg) of 4-nitro-1H-pyrrolo-[2,3-b]pyridine 7-oxide and 3-nitro-1H-pyrrolo[2,3-b]pyridine-7-oxide in N,N-dimethylformamide (6 ml) was added dropwise methanesulfonyl chloride (0.68 ml) at 65° C. The reaction mixture was stirred at 65° C. for 2 hours. The reaction mixture was quenched with water (30 ml) under ice cooling, and neutralized (pH ˜6.5) with 20% NaOH solution. The resulting precipitates were collected by filtration, dried in vacuo at 40° C., and washed with EtOAc to give 4-chloro-3-nitro-1H-pyrrolo[2,3-b]pyridine (172.8 mg) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163767B2
Source datasetuspto-grants-2012_04
ORD IDord-3323f3aa8e9c4f79a838f55180926f97
Source noteuspto-grants-2012_04