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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992406Generated: October 31, 2026

Indole → HCID 131723561, compound

https://huagongshe.com/reaction/992406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantDimethyl SulfideHCID 1068—
ReactantL-TryptophanHCID 6305—
ReactantTrifluoroacetic acidHCID 6422—
Reactant1,2-EthanedithiolHCID 10902—
ReactantHCID 131723562HCID 131723562—
SolventDichloromethaneHCID 6344—
ProductHCID 131723561HCID 13172356178.5%

Reaction Steps

Under N2 atmosphere, the Boc-DTrp-DPro-diisobutylamide was dissolved in 25 ml of CH2Cl2, 1 ml of methylsulfide and 0.5 ml of 1,2-ethanedithiol was added as scavenger in suppressing the indole alkylation of tryptophane. 10 ml of trifluoracetic acid was added dropwise while being stirred. The reaction mixture was stirred for 30 min. Volatiles were removed under vacuum and the residue was dissolved in 30 ml of CH2Cl2 and washed with 10 ml saturated NaHCO3 aqueous solution. The organic layer was dried over anhydrous sodium sulfate and filtered and the solvents were removed in vacuum. The residue was further purified by column chromatography (SiO2, CHCl2/MeOH, 85:15) to afford 0.55 mmol (78.5%) of compound (2) which was characterized by TLC and mass spectra, M+=411.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06468974B1
Source datasetuspto-grants-2002_10
ORD IDord-2f0dc489546240478d0541929f0723d2
Source noteuspto-grants-2002_10