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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401969Generated: October 30, 2026

2,4-Dimethoxybenzylamine → Ethyl 4-cyano-5-[(2,4-dimethoxybenzyl)amino]-3-iodothiophene-2-carboxylate

https://huagongshe.com/reaction/2401969

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DimethoxybenzylamineHCID 597250—
ReactantEthyl 4-cyano-3-iodo-5-(methylsulfonyl)thiophene-2-carboxylateHCID 40152062—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-cyano-5-[(2,4-dimethoxybenzyl)amino]-3-iodothiophene-2-carboxylateHCID 5925003181%

Reaction Conditions

Temperature60 °C

Reaction Steps

Ethyl 4-cyano-3-iodo-5-(methylsulfonyl)thiophene-2-carboxylate (5.60 g, 0.0145 mol) and 2,4-dimethoxybenzylamine (3.51 mL, 0.0234 mol) were combined in tetrahydrofuran (100 mL) and stirred at 60° C. for 3 days. The reaction was concentrated in vacuo, diluted with dichloromethane and hexanes and the resultant precipitate was filtered to yield the title compound (5.56, 81%) as a yellow solid. LCMS: (FA) ES+, 473. 1H NMR (400 MHz, d6-DMSO) δ: 9.05 (s, 1H) 7.10 (d, 1H, J=8.57 Hz), 6.60-6.50 (m, 2H), 4.30 (s, 2H), 4.22-4.14 (m, 2H), 3.80 (s, 3H), 3.75 (s, 3H), 1.26-1.21 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796271B2
Source datasetuspto-grants-2014_08
ORD IDord-4a1009fab00d4e5dbbbcbeae6d2abd7a
Source noteuspto-grants-2014_08