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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530922Generated: October 30, 2026

Hydrochloric Acid → 3-(Dimethylaminomethyl)-7-azaindole

https://huagongshe.com/reaction/530922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
Reactant1H-Pyrrolo(2,3-b)pyridineHCID 9222—
ReactantDimethylamine, hydrochlorideHCID 10473—
Solvent1-ButanolHCID 263—
SolventWaterHCID 962—
Solventtert-Butyl methyl etherHCID 15413—
Product3-(Dimethylaminomethyl)-7-azaindoleHCID 538354980.5%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a mixture of 7-azaindole (150 g), dimethylamine hydrochloride (114 g) and 1-butanol (1.275 L) was added a 37% aqueous formaldehyde solution (103 g), and the mixture was stirred on a 120° C. oil bath for 2.5 hours. The reaction solution was cooled to around 40° C., and placed into water (1.35 L), concentrated hydrochloric acid (54 mL) and methyl tert-butyl ether (MTBE) (630 mL) were added, the mixture was stirred, the layers were separated, and the aqueous layer was taken. This aqueous layer was further washed with MTBE, and a 48% aqueous sodium hydroxide solution was added. This was extracted with chloroform, and a small amount of methanol was added to the extraction solution, followed by drying with anhydrous sodium sulfate. A desiccant was distilled off, followed by concentration under reduced pressure, to obtain the title compound (179 g) having the following physical property values.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353113B2
Source datasetuspto-grants-2016_05
ORD IDord-8fccccd32555449db4d502ba771a4b2c
Source noteuspto-grants-2016_05