Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250683Generated: November 1, 2026

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

https://huagongshe.com/reaction/250683

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 numberUS07863288B2
Source datasetuspto-grants-2011_01
ORD IDord-f2f89346cbce4fc0be87113eb75b25ab
Source noteuspto-grants-2011_01