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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754646Generated: October 27, 2026

Methanol → (6-chloro-2-methoxypyridin-3-yl)(1H-pyrrolo[2,3-b]pyridin-3-yl)methanol

https://huagongshe.com/reaction/1754646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1H-Pyrrolo(2,3-b)pyridineHCID 9222—
ReactantPotassium HydroxideHCID 14797—
Reactant6-Chloro-2-methoxypyridine-3-carbaldehydeHCID 10855945—
SolventDichloromethaneHCID 6344—
Product(6-chloro-2-methoxypyridin-3-yl)(1H-pyrrolo[2,3-b]pyridin-3-yl)methanolHCID 5959334255.1%

Reaction Steps

To 1H-Pyrrolo[2,3-b]pyridine (1, 0.455 g, 3.85 mmol) and 6-chloro-2-methoxypyridine-3-carbaldehyde (26, 0.661 g, 3.85 mmol) was added methanol (10 mL) followed by potassium hydroxide (0.310 g, 5.52 mmol). The reaction was allowed to stir at room temperature overnight. The reaction was extracted with diethyl ether/ethyl acetate and water. The organic layer was separated, dried over anhydrous magnesium sulfate, filtered and volatiles were removed by rotary evaporation to provide a solid that was treated with dichloromethane and stored in a freezer overnight. The white solid was collected by vacuum filtration and dried in vacuo to give 613 mg of compound 27 (2.12 mmol, 55%). MS (ESI) [M+H+]+=290.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169250B2
Source datasetuspto-grants-2015_10
ORD IDord-1df9312c356a4914a7dd908185732d94
Source noteuspto-grants-2015_10