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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506025Generated: November 4, 2026

Iodoethane → HCID 11521901, compound

https://huagongshe.com/reaction/506025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
Reactant2-Amino-6-nitro-1H-indole-3-carbonitrileHCID 16361367—
ReactantHCID 59425037HCID 59425037—
SolventDimethyl SulfoxideHCID 679—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 11521901HCID 11521901—

Reaction Steps

Sodium hydride (42 mg, 1.05 mmol, 60% w/w suspension in mineral oil) is washed with hexane and taken up in dimethylsulfoxide (1 mL). A solution of 2-amino-6-nitro-1H-indole-3-carbonitrile (prepared in procedure 1T) in dimethylsulfoxide (1 mL) is added by syringe, and the resulting mixture is stirred for 20 min. Then, iodoethane (77 μL, 0.96 mmol) is added by syringe, and the mixture is stirred for 14 h. The reaction is then poured into EtOAc (50 mL), and this solution is washed with water (3×50 mL) and saturated brine (40 mL). The aqueous phases are back-extracted with EtOAc, and the organic extracts are combined, dried over Na2SO4, filtered and evaporated. The residual material is separated by column chromatography over silica gel (EtOAc/hexanes, 1/1) to afford first a small amount of a dialkylated analog, then the desired compound, 2-amino-1-ethyl-6-nitro-1H-indole-3-carbonitrile (114 mg, 52%), and finally unreacted starting material. The desired product is isolated as an orange powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781478B2
Source datasetuspto-grants-2010_08
ORD IDord-e6943f3a33274d7aa8e5754867934c53
Source noteuspto-grants-2010_08