Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980291Generated: October 30, 2026

Ethanol → HCID 12822508, compound

https://huagongshe.com/reaction/980291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHCID 12822471HCID 12822471—
SolventEthyl formateHCID 8025—
ProductHCID 12822508HCID 12822508—

Reaction Steps

A solution of N-[[3-(2-aminoethyl)-1H-indol-5-yl]methyl]methanesulphonamide (2.1 g) in ethanol (20 ml) and ethyl formate (25 ml) was refluxed for 17 h. The solvent was evaporated in vacuo and the residue was partitioned between sulphuric acid (1N; 100 ml) and ethyl acetate (150 ml). The aqueous layer was extracted with ethyl acetate (150 ml) and the combined organic extracts were washed with brine (50 ml) and potassium carbonate solution (15%; 50 ml) and dried (Na2SO4). Evaporation of the solvent in vacuo gave the crude product as a very viscous oil (2.2 g). The oil was dissolved in THF (8 ml), scratched and left overnight at room temperature. Filtration gave the title compound (1.3 g) as a white solid m.p. 121°-5°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04636521
Source datasetuspto-grants-1987_01
ORD IDord-0ac6db0a320a4967ba188ab6e8030e40
Source noteuspto-grants-1987_01