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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356316Generated: October 30, 2026

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

https://huagongshe.com/reaction/356316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
Reactant1,5-Diazabicyclo(4.3.0)non-5-eneHCID 76349—
ReactantHCID 137331292HCID 137331292—
SolventDimethylformamideHCID 6228—
Productethyl 1-methyl-1H-pyrrolo[2,3-b]pyridine-2-carboxylateHCID 2329833527.6%

Reaction Steps

A solution of 994 mg of ethyl 3-t-butyldimethyl-silyloxy-3-(2-chloropyridin-3-yl)-2-methylaminopropionate (prepared as described in Preparation 79) and 393 mg of 1,5-diazabicyclo[4.3.0]non-5-ene in 5 ml of dimethylformamide was stirred at 150° C. for 5 hours. At the end of this time, the reaction mixture was poured into a saturated aqueous solution of amnmonium chloride, after which it was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous sodium sulfate, after which the solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography through silica gel, using a gradient elution method, with mixtures of hexane and ethyl acetate in ratios ranging from 9:1 to 5:1 by volume as the eluent, to give 150 mg of the title compound having Rf=0.40 (on silica gel thin layer chromatography using a 3:1 by volume mixture of hexane and ethyl acetate as the developing solvent).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834501
Source datasetuspto-grants-1998_11
ORD IDord-d2df987e9fb84ce6ac8be271ed55d60f
Source noteuspto-grants-1998_11