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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261139Generated: October 30, 2026

Water → (5-Bromo-1H-pyrrolo[2,3-b]pyridin-3-yl)(4-methoxyphenyl)methanone

https://huagongshe.com/reaction/1261139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Anisoyl chlorideHCID 7477—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant5-bromo-1H-pyrrolo[2,3-b]pyridineHCID 10307932—
SolventDichloromethaneHCID 6344—
Product(5-Bromo-1H-pyrrolo[2,3-b]pyridin-3-yl)(4-methoxyphenyl)methanoneHCID 58086686—

Reaction Steps

Aluminum trichloride (2.7 g, 20.0 mmol) and methylene chloride (30 mL) were combined under an atmosphere of nitrogen and 5-bromo-7-azaindole (67, 400.0 mg, 2.30 mmol) in methylene dichloride (20 mL) was added. The reaction was stirred at room temperature for 70 minutes. 4-Methoxybenzoic acid chloride (0.38 g, 2.2 mmol) (prepared from the corresponding carboxylic acid using the protocol described in Example 1, Scheme 13, Step 4) in methylene dichloride (7.0 mL) was added. The reaction was stirred at room temperature for 2 hours, then poured into water and extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, and concentrated to give the compound (116, 250 mg, 34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470818B2
Source datasetuspto-grants-2013_06
ORD IDord-dc2dac8c701f4c9889f0ccafdced92f2
Source noteuspto-grants-2013_06