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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097256Generated: October 26, 2026

Water → ethyl 1-(phenylmethyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylate

https://huagongshe.com/reaction/1097256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 1H-pyrrolo(2,3-b)pyridine-2-carboxylateHCID 21868741—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Productethyl 1-(phenylmethyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylateHCID 4460825782%

Reaction Conditions

Temperature20 °C

Reaction Steps

2 g (10 mmol) of ethyl pyrrolo[2,3-b]pyridine-2-carboxylate (WO2004101563) are added, portionwise, to a suspension of 0.44 g (11 mmol) of sodium hydride in 50 ml of DMF, stirred at 20° C. After stirring at ambient temperature for 1 h, 2.1 g (12 mmol) of benzyl bromide are added, dropwise, and the reaction mixture is stirred at ambient temperature for 20 h. 150 ml of water and 150 ml of ethyl ether are subsequently added with stirring. The aqueous phase is separated and extracted twice with 50 ml of ethyl ether. The organic phases are combined, washed with 100 ml of water, dried over sodium sulphate and then concentrated under reduced pressure. The resulting product is purified by silica column chromatography, elution being carried out with a mixture of heptane and dichloromethane. 2.3 g of the expected product are thus isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143248B2
Source datasetuspto-grants-2012_03
ORD IDord-93b54ec49f9b4c8bafb37fe70ad6cbdf
Source noteuspto-grants-2012_03