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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252518Generated: October 30, 2026

Iodoethane → HCID 11521901, compound

https://huagongshe.com/reaction/252518

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 numberUS07868037B2
Source datasetuspto-grants-2011_01
ORD IDord-ebc88bd6b25140569a396d90a9612bdc
Source noteuspto-grants-2011_01