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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947554Generated: October 31, 2026

Diethyl (ethoxymethylene)malonate → Diethyl 2-((thiophen-3-ylamino)methylene)malonate

https://huagongshe.com/reaction/1947554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant1-MethylpiperazineHCID 53167—
ReactantMethyl 3-amino-2-thiophenecarboxylateHCID 89652—
SolventAcetonitrileHCID 6342—
ProductDiethyl 2-((thiophen-3-ylamino)methylene)malonateHCID 2807580—

Reaction Steps

A mixture of methyl 3-aminothiophene-2-carboxylate 1 (5.0 g, 32 mmol, 1.0 eq), N-methyl piperazine (6.5 g, 64 mmol, 2.0 eq) and NMP (30 mL) was heated to reflux for 16 hours. After the decarboxylation was complete, the reaction mixture was allowed to cool to room temperature and diethyl 2-(ethoxymethylene)-malonate (7.0 g, 32 mmol, 2.0 eq) was added. The reaction mixture was heated to reflux for 4 h. The product was purified using SiO2 column chromatography (Hex/EtOAc; 100:0 to 80:20%) to obtain a light yellow powder, 5.0 g (31%). LC/MS (10-99% CH3CN/0.05% TFA gradient over 5 min): m/z 270.2, retention time 1.52 minutes. 1H NMR (DMSO-d6) δ: 10.80 (d, 1.0 H, J=13.87 Hz, NH), 8.30 (d, 1.0 H, J=13.94 Hz), 7.60 (dd, 1.0H, J=3.0 Hz, J′=2.0 Hz), 7.40 (dd, 1.0 H, J=1.5 Hz, J′=3.13 Hz), 7.28 (dd, 1.0 H, J=1.5 Hz, J′=5.2 Hz), 4.20 (q, 2H, J=7.0 Hz), 4.10 (q, 2H, J=7.0 Hz), 1.30 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399479B2
Source datasetuspto-grants-2013_03
ORD IDord-679022f7a63d49a2a10ae9b6c4961527
Source noteuspto-grants-2013_03