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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769211Generated: October 30, 2026

Formaldehyde → HCID 18946789, compound

https://huagongshe.com/reaction/1769211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant1H-Pyrrolo(2,3-b)pyridineHCID 9222—
ReactantDimethylamine, hydrochlorideHCID 10473—
Solvent1-ButanolHCID 263—
ProductHCID 18946789HCID 1894678988.2%

Reaction Steps

To 40 ml of n-butyl alcohol was added 1.18 g of 7-azaindole, 0.88 g of dimethylamine hydrochloride and 0.33 g of paraformaldehyde, and the mixture refluxed for 30 minutes. The clear solution was then evaporated to dryness in vacuo, and 10 ml of 10% aqueous hydrochloric acid was added to the residue. The water layer was extracted with ether, and then made strongly basic with potassium carbonate. The resulting precipitate was filtered off, washed with ether and dried, yielding 1.42 g (81.1%) of 3-dimethylamino-7-azaindole, m.p. 144°-152° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05380739
Source datasetuspto-grants-1995_01
ORD IDord-682775b56be642198c6b2debcc89c777
Source noteuspto-grants-1995_01