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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601850Generated: November 2, 2026

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

https://huagongshe.com/reaction/1601850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1,5-Diazabicyclo(4.3.0)non-5-eneHCID 76349—
ReactantEthyl 3-t-butyldimethylsilyloxy-3-(2-chloropyridin-3-yl)-2-methylaminopropionateHCID 23298295—
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-butyldimethylsilyloxy-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 ammonium 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 numberUS05977365
Source datasetuspto-grants-1999_11
ORD IDord-e4476e059b9547588ab1fe876efc42db
Source noteuspto-grants-1999_11