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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582844Generated: October 30, 2026

Iodoethane → HCID 15435226, compound

https://huagongshe.com/reaction/582844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantCesium carbonateHCID 10796—
ReactantPotassium CarbonateHCID 11430—
Reactant1H-Indole-3-carboxamide, N-(4-ethoxyphenyl)-4,5,6,7-tetrahydro-4-oxo-HCID 9948191—
SolventDimethylformamideHCID 6228—
ProductHCID 15435226HCID 1543522632%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of N-(4-ethoxyphenyl)-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxamide (204 mg, 0.7 mmol), potassium carbonate (188 mg, 1.4 mmol), cesium carbonate (22 mg, 0.1 mmol), and iodoethane (0.08 mL, 1 mmol) in N,N-dimethylformamide was heated at 85° C. for 1 hour. The mixture was cooled and filtered using ethyl acetate. The solid was set aside; the organic layer was washed with water, dried over magnesium sulfate, filtered, concentrated in vacuo, and triturated with diethyl ether to give N-(4-ethoxyphenyl)-1-ethyl-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxamide (73 mg). The set-aside solid was slurried in aqueous hydrochloric acid, the precipitate collected, rinsed with water and dried to give additional amide (Compound 58) (94 mg). mp. 209-210° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05925770
Source datasetuspto-grants-1999_07
ORD IDord-b3b1741ba3884f17a771d02dbfb56411
Source noteuspto-grants-1999_07