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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785593Generated: October 30, 2026

Dichloromethane → HCID 67005759, compound

https://huagongshe.com/reaction/1785593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant3,5-Dimethoxybenzyl BromideHCID 1274490—
Reactant5-bromo-1H-pyrrolo[2,3-b]pyridineHCID 10307932—
ReactantHCID 178418573HCID 178418573—
CatalystZincchlorideHCID 3007855—
ProductHCID 67005759HCID 670057594.4%

Reaction Steps

Into a round bottom flask, under an atmosphere of nitrogen, methylmagnesium bromide (0.16 mL, 1.4 mmol) was added to a solution of 7-azaindole (1) (0.150 g, 1.27 mmol) in anhydrous methylene chloride (12 mL, 0.19 mol), at room temperature. The resulting mixture was stirred at room temperature for one hour before zinc dichloride (0.21 g, 1.5 mmol) was added. After stirring for an additional hour, 3,5-dimethoxybenzyl bromide (4) (0.35 g, 1.5 mmol) was added into the reaction mixture. The reaction was stirred overnight at room temperature before it was quenched with methanol. The mixture was evaporated to dryness, dissolved into ethyl acetate and washed with water. The aqueous portion was neutralized with sodium bicarbonate (s.s.) and extracted with ethyl acetate (3×). Organic portions were combined and washed with 0.1N HCl, dried over anhydrous sodium sulfate and evaporated under reduced pressure. Purification by preparative TLC with 50% ethyl acetate/hexane gave Compound 29 as a yellow powder (15 mg; M+H=269.2, M−H=267.2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504509B2
Source datasetuspto-grants-2009_03
ORD IDord-8988b9ac601a49c4bc8d816c13dd86ed
Source noteuspto-grants-2009_03