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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380575Generated: November 3, 2026

Hydrochloric Acid → HCID 12851454, compound

https://huagongshe.com/reaction/1380575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantDimethylamine, hydrochlorideHCID 10473—
Reactant1-[2-(3-Ethyl-5-methyl-1,2-oxazol-4-yl)-1H-indol-3-yl]ethan-1-oneHCID 12851453—
SolventEthanolHCID 702—
ProductHCID 12851454HCID 12851454—

Reaction Steps

A mixture of 12 g. (0.045 mole) of 2-(3-ethyl-5-methyl-4-isoxazolyl)-3-acetyl indole, 4 g. (0.049 mole) of dimethylamine hydrochloride, and 0.5 ml. concentrated hydrochloric acid in 70 ml. of ethanol is heated to reflux and treated by portionwise addition with 14 g. (0.470 mole) of paraformaldehyde over 5 hours. The resulting mixture is refluxed an additional 24 hours, cooled and evaporated in vacuo. The residue is then dissolved in 300 ml. methylene chloride and washed with 200 ml. 2N hydrochloric acid. The aqueous acid is cooled and made basic with 2N sodium hydroxide and extracted with methylene chloride. The organic layer is dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo. The residue is crystallized from ether to give 3-dimethylamino-1-[2-(3-ethyl-5-methyl-4-isoxazolyl)-1H-indole-3-yl]-1-propanone, m.p. 146°-148° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04582848
Source datasetuspto-grants-1986_04
ORD IDord-0277b409438e45d98a090a531d97ffca
Source noteuspto-grants-1986_04