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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172786Generated: November 2, 2026

Sodium Bicarbonate → N-(2,4-dimethoxybenzyl)-N-prop-2-yn-1-yl-1H-pyrrole-2-carboxamide

https://huagongshe.com/reaction/1172786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant1-[(1H-Pyrrol-2-ylcarbonyl)oxy]-2,5-pyrrolidinedioneHCID 6421660—
ReactantN-(2,4-dimethoxybenzyl)prop-2-yn-1-amineHCID 28419238—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductN-(2,4-dimethoxybenzyl)-N-prop-2-yn-1-yl-1H-pyrrole-2-carboxamideHCID 86633422—

Reaction Steps

A solution of 1-[(1H-pyrrol-2-ylcarbonyl)oxy]pyrrolidine-2,5-dione (1 eq), N-(2,4-dimethoxybenzyl)prop-2-yn-1-amine (1.05 eq) and NaHCO3 (1 eq) in a mixture of CH3CN and H2O (20:1) was heated at reflux for 12 hrs and then the MeCN was removed under reduced pressure. The resulting residue was partitioned between DCM and sat. aq. NaHCO3 solution. The organic phase was dried (Na2SO4), filtered, concentrated under reduced pressure and the resulting brown oil was purified by Biotage system eluting with EtOAc/petrol ether to obtain the desired amide. MS (ES) C17H18N2O3 requires: 298, found: 299 (M+H)+. 1H NMR (300 MHz, DMSO-d6) δ: 11.56 (1H, br. S), 7.40 (1H, d, J=8.3 Hz), 6.91 (1H, s), 6.60 (1H, d, J=2.1 Hz), 6.52 (1H, dd, J=8.3, 2.1 Hz), 6.48-6.35 (1H, m), 6.09 (1H, s), 4.68 (2H, s), 4.22 (2H, s), 3.80 (3H, s), 3.76 (3H, s), 3.24 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834015B2
Source datasetuspto-grants-2010_11
ORD IDord-097b6373631244b790c3d744c4039a1f
Source noteuspto-grants-2010_11