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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367281Generated: October 27, 2026

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

https://huagongshe.com/reaction/1367281

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 numberUS07893075B2
Source datasetuspto-grants-2011_02
ORD IDord-5b1f866dad394a2e958b5b70750a17aa
Source noteuspto-grants-2011_02