Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172787Generated: November 2, 2026

2-Fluoro-5-iodobenzonitrile → N-[3-(3-Cyano-4-fluorophenyl)prop-2-yn-1-yl]-N-(2,4-dimethoxybenzyl)-1H-pyrrole-2-carboxamide

https://huagongshe.com/reaction/1172787

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-5-iodobenzonitrileHCID 2778928—
ReactantN-(2,4-dimethoxybenzyl)-N-prop-2-yn-1-yl-1H-pyrrole-2-carboxamideHCID 86633422—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductN-[3-(3-Cyano-4-fluorophenyl)prop-2-yn-1-yl]-N-(2,4-dimethoxybenzyl)-1H-pyrrole-2-carboxamideHCID 68688798—

Reaction Steps

To a solution of A1 (1 eq) in a mixture of DMF and Et3N (1:1) was added 2-fluoro-5-iodobenzonitrile (2 eq), CuI (0.2 eq) and Pd(PPh3)4 (0.05 eq). The resulting mixture was stirred at RT overnight. The reaction mixture was diluted with EtOAc, washed with 0.1N HCl (2×) and then with brine; dried (Na2SO4) and concentrated. The resulting crude was purified by on silica gel eluting with EtOAc/petrol ether to obtain the desired compound. MS (ES) C24H20FN3O3 requires: 417, found: 418 (M+H)+. 1H NMR (400 MHz, DMSO-d6) δ: 11.59 (1H, bs), 7.93 (1H, dd, J=6.3, 2.0 Hz), 7.78-7.73 (1H, m), 7.53 (1H, t, J=9.1 Hz), 7.13 (1H, d, J=8.3 Hz), 6.93 (1H, s), 6.60 (1H, d, J=2.3 Hz), 6.53 (1H, dd, J=8.3, 2.3 Hz), 6.50-6.38 (1H, m), 6.10 (1H, s), 4.77 (2H, s), 4.50 (2H, s), 3.78 (3H, s), 3.76 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834015B2
Source datasetuspto-grants-2010_11
ORD IDord-bafd89f6352b450d86ae6d56c0bc2fbd
Source noteuspto-grants-2010_11