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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404982Generated: October 31, 2026

Triethylamine → HCID 69080726, compound

https://huagongshe.com/reaction/2404982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIodobenzeneHCID 11575—
ReactantHCID 86626642HCID 86626642—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystPalladium, tris[mu-[(1,2-eta:4,5-eta)-(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one]]di-, compd. with trichloromethane (1:1)HCID 11029508—
SolventDimethylformamideHCID 6228—
ProductHCID 69080726HCID 690807266.6%

Reaction Steps

Tris(dibenzylideneacetone)dipalladium(0) chloroform adduct (62.1 mg, 0.03 eq.), 4-iodobenzene (0.45 g, 1.1 eq.), triethylamine (0.61 g, 3 eq.), and copper (1) iodide (23 mg, 0.06 eq.) were added sequentially to a solution of 2-ethyl-1-(2-propynyl)-1H-imidazo[4,5-c]quinolin-4-amine (0.5 g, 2.0 mmol, 1.0 eq) in DMF. The reaction mixture was stirred at ambient temperature overnight. The reaction mixture was concentrated under reduced pressure to provide crude product which was purified by column chromatography (silica gel eluting with 8/92 methanol/dichloromethane). The residue was purified by recrystallization from 1,2-dichloroethane to provide 60 mg of 2-ethyl-1-(3-phenyl-2-propynyl)-1H-imidazo[4,5-c]quinolin-4-amine hydroiodide as a brown powder, mp 200-212° C. (dec). 1H NMR (300 MHz, DMSO-d6) δ 13.25 (s, 1H), 8.79 (br, 2H), 8.53 (dd, J=0.9, 8.5 Hz, 1H), 7.86 (dd, J=0.9, 8.3 Hz, 1H), 7.74 (ddd, J=1.2, 7.2, 8.4 Hz, 1H), 7.66 (ddd, J=1.2, 7.2, 8.3 Hz, 1H), 7.36 (m, 5H), 5.82 (s, 2H), 3.15 (q, J=7.5 Hz, 2H), 1.43 (t, J=7.5 Hz, 3H); MS (APCI) m/z 327 (M+H)+; Anal. Calcd for C21H18N4.HI: C, 55.52; H, 4.22; N, 12.33. Found: C, 55.80; H, 3.94; N, 12.46.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802853B2
Source datasetuspto-grants-2014_08
ORD IDord-8d78b3baea0a42dfb206b6a49bb25148
Source noteuspto-grants-2014_08