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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994363Generated: October 26, 2026

Indole → [2-(1H-Indol-3-ylsulfanyl)benzyl]methylamine

https://huagongshe.com/reaction/1994363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantTrichloroacetic AcidHCID 6421—
ReactantSodium HydroxideHCID 14798—
Reactant2-Methyl-2,3-dihydro-benzo[d]isothiazoleHCID 12428808—
ReactantEthyl acetate methanol triethylamineHCID 21980445—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product[2-(1H-Indol-3-ylsulfanyl)benzyl]methylamineHCID 1597984867%

Reaction Steps

2-Methyl-2,3-dihydro-benzoisothiazole (VI) (Hoffmann, R. W.; Goldman, S. Chem. Ber. 111, 1978, 2716-2725) (75 mg, 0.50 mmol) was dissolved in THF (1 mL) and added to indole (V) (140 mg, 0.60 mmol) under Ar. Tricloroacetic acid (90 mg, 0.55 mmol) was added and the reaction mixture was stirred at room temperature for 16 hours. 2 mL 1N NaOH (aq) was added. Extraction with ethyl acetate (2×10 mL) and purification by flash chromatography on silica gel (eluent: ethyl acetate then ethyl acetate/methanol/triethylamine) gave 88 mg [2-(1H-Indol-3-ylsulfanyl)benzyl]methyl amine (67% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652150B2
Source datasetuspto-grants-2010_01
ORD IDord-fc32bc8f0bfa42c1a8aa4f517dea1c04
Source noteuspto-grants-2010_01