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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766149Generated: October 31, 2026

Methanol → methyl 1H-pyrrolo[2,3-b]pyridine-3-carboxylate

https://huagongshe.com/reaction/1766149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant1H-Pyrrolo(2,3-b)pyridine-3-carboxylic acidHCID 10154191—
Productmethyl 1H-pyrrolo[2,3-b]pyridine-3-carboxylateHCID 21110084—

Reaction Steps

4.22 g (26 mmol) of 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid were added to 100 cm3 of methanol at a temperature in the region of 20° C. and then 2.5 cm3 of concentrated sulfuric acid were run in dropwise. After stirring at reflux of the solvent for 16 h, the reaction medium was concentrated to dryness under reduced pressure (2.7 kPa). The residue was rapidly added to 50 cm3 of water and the pH was adjusted to 8 by addition of 1N sodium hydroxide. After extracting with 300 cm3 of ethyl acetate, the organic phase was washed with 2 times 100 cm3 of water and then 100 cm3 of saturated aqueous sodium chloride solution. After drying over magnesium sulfate and then concentrating to dryness under reduced pressure (2.7 kPa), 3.7 g of methyl 1H-pyrrolo[2,3-b]pyridine-3-carboxylate were obtained in the form of a yellow powder. Mass spectrum: EI: m/z=176 M+; base pic: m/z=145 (M−CH3O)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230007B2
Source datasetuspto-grants-2007_06
ORD IDord-e7d5cf92bc6d4825949f65309d69a122
Source noteuspto-grants-2007_06