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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749507Generated: November 1, 2026

Tryptamine → HCID 118162234, compound

https://huagongshe.com/reaction/1749507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTryptamineHCID 1150—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,4-Dichloro-5-cyanopyrimidineHCID 14026907—
SolventTetrahydrofuranHCID 8028—
ProductHCID 118162234HCID 11816223438.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 2,4-dichloro-pyrimidine-5-carbonitrile (2.0 g, 11.5 mmol), 2-(1H-indol-3-yl)-ethylamine (1.83 g, 11.4 mmol), and DIEA (1.94 g, 15.0 mmol) in THF (50 mL) was stirred at 50° C. for 3 h. After cooling to room temperature, the reaction mixture was concentrated and the residue was diluted with ethyl acetate (150 mL). The organic layer was washed with saturated aqueous ammonium chloride, brine, dried over anhydrous sodium sulfate and filtered. The filtrate was evaporated in vacuum to give the crude product, which was purified by silica gel column chromatography (20% ethyl acetate in petroleum ether) to afford the title compound as a brown solid (1.3 g, 4.38 mmol, 38% yield). MS (ESI) m/z 298.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156798B2
Source datasetuspto-grants-2015_10
ORD IDord-b4fd60a5ad124363acf4dd5581a2ed73
Source noteuspto-grants-2015_10