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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129224Generated: October 31, 2026

Trifluoroacetic acid → HCID 19372789, compound

https://huagongshe.com/reaction/129224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
ReactantHCID 19372801HCID 19372801—
SolventDichloromethaneHCID 6344—
ProductHCID 19372789HCID 1937278973.5%

Reaction Steps

To a suspension of 4-amino-3,4-dihydro-6-methoxy-1-p-toluenesulfonylbenz[cd]indol-5(1H)-one hydrochloride (1.45 g, 3.50 mmol) in dichloromethane (30 ml) were added, while stirring under ice-cooling, anhydrous trifluoroacetic acid (0.61 ml, 4.27 mmol) and triethylamine (1.18 ml, 16.1 mmol). The mixture was stirred for 30 minutes as it was. After completion of the reaction, the reaction mixture was subjected to distillation under reduced pressure. The residue was shaken together with ethyl acetate (40 ml)-1N HCl (30 ml) to allow two layers to be formed. The organic layer was washed with an aqueous saline solution and dried (anhydrous Na2SO4). The solvent was distilled off under reduced pressure. The residue was recrystallized from ethyl acetate-n-hexane to afford the title compound (1.2 g, 73%, m.p.189°-190° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05466689
Source datasetuspto-grants-1995_11
ORD IDord-5db5b489605349bcb6b59c753c4a0d29
Source noteuspto-grants-1995_11