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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243074Generated: October 30, 2026

Tryptamine → HCID 21940715, compound

https://huagongshe.com/reaction/1243074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTryptamineHCID 1150—
ReactantIodobenzeneHCID 11575—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactanttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 21940715HCID 2194071587.2%

Reaction Steps

Using the general procedure, tryptamine (0.160 g, 1.00 mmol) was coupled with iodobenzene (134 μL, 1.20 mmol) using CuI (9.5 mg, 0.050 mmol, 5.0 mol %), K3PO4 (2.1 mmol), trans-N,N′-dimethyl-1,2-cyclohexanediamine (32 μL, 0.20 mmol, 20 mol %) and toluene (1.0 mL) to give the crude product. Column chromatography (2×15 cm, methylene chloride (saturated with ammonia):methanol 50:1) provided 0.206 g (87% yield) of the product as a yellow oil. 1H NMR (400 MHz, CDCl3): δ 7.65 (m, 1H), 7.55 (m, 1H), 7.47 (m, 4H), 7.31 (m, 1H), 7.18 (m, 3H), 3.06 (t, J=7 Hz, 2H), 2.94 (t, J=7 Hz, 2H), 1.40 (bs, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115784B2
Source datasetuspto-grants-2006_10
ORD IDord-9cfe64c2ec904940871ada1c20845697
Source noteuspto-grants-2006_10