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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572600Generated: October 31, 2026

Ethyl iodoacetate → Ethyl 4-cyano-3-(2,4-dichlorophenyl)-5-morpholin-4-ylthiophene-2-carboxylate

https://huagongshe.com/reaction/572600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl iodoacetateHCID 12183—
Reactant2,4-Dichlorobenzoyl chlorideHCID 66645—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Morpholin-4-yl-3-thioxopropanenitrileHCID 45158941—
SolventAcetonitrileHCID 6342—
ProductEthyl 4-cyano-3-(2,4-dichlorophenyl)-5-morpholin-4-ylthiophene-2-carboxylateHCID 4415589828%

Reaction Steps

A solution of 3-morpholin-4-yl-3-thioxopropanenitrile (0.150 g, 0.88 mmol) in anhydrous ACN (1.2 mL) was cooled to 0° C. To this cooled solution was added of 2,4-dichlorobenzoyl chloride (0.149 mL, 1.06 mmol) and DIPEA (0.161 mL, 0.93 mmol). The mixture was allowed to stir at rt under nitrogen for 15 min before ethyl iodoacetate (0.10 mL, 0.93 mmol) and DIPEA (0.161 mL, 0.93 mmol) were added. The reaction mixture was subjected to MWI at 140° C. for 10 min. The mixture was allowed to cool and was concentrated. The residue was purified by column chromatography to give ethyl 4-cyano-3-(2,4-dichlorophenyl)-5-morpholin-4-ylthiophene-2-carboxylate (78) (0.1 g, 28%). LCMS: (AA) ES+ 411.09. 1H NMR (400 MHz, CDCl3) δ: 7.49 d, 1H), 7.33 (dd, 1H), 7.20 (d, 1H), 4.08-4.16 (m, 2H), 3.85-3.89 (m, 4H), 3.63-3.66 (m, 4H) and 1.12 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029411B2
Source datasetuspto-grants-2015_05
ORD IDord-2a1af50d26f54388abc6e7224476bd10
Source noteuspto-grants-2015_05