Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868422Generated: October 25, 2026

Aziridine → HCID 11504035, compound

https://huagongshe.com/reaction/1868422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAziridineHCID 9033—
ReactantSodium hydrideHCID 24758—
Reactant3-PhenylindoleHCID 96502—
Reactant2-Trifluoromethyl-1-(2,4,6-trimethylbenzenesulfonyl)aziridineHCID 57474036—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
ProductHCID 11504035HCID 1150403572.3%

Reaction Steps

To a solution of 48 mg (0.25 mmol) of 3-phenyl-1H-indole in 3 mL of DMF was added 28 mg (0.7 mmol) of 60% sodium hydride in mineral oil. The mixture stirred until hydrogen evolution ceased and then 73 mg (0.25 mmol) of 2-trifluoromethyl-1-(2,4,6-trimethylbenzenesulfonyl)aziridine was added. The reaction was monitored by TLC (20% EtOAc-hexanes and 50% hexanes-CH2Cl2) indicating starting aziridine was consumed. After 30 minutes, the mixture was quenched with 7 mL of saturated aqueous ammonium chloride solution and extracted with three 7 mL portions of ethyl acetate. The combined organic layers were washed with three 7 mL portions of saturated aqueous ammonium chloride solution and three 7 mL portions of brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was triturated with ether to afford 88 mg (72%) of the title compound. MS: m/z 487.59 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635711B2
Source datasetuspto-grants-2009_12
ORD IDord-aa2b08c421de4568a875b676811756a6
Source noteuspto-grants-2009_12