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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172881Generated: October 26, 2026

Aniline → Ethyl 6-(2-anilino-2-oxoethyl)-1-benzothiophene-2-carboxylate

https://huagongshe.com/reaction/1172881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant[2-(Ethoxycarbonyl)-1-benzothien-6-yl]acetic acidHCID 59424238—
SolventDimethylformamideHCID 6228—
ProductEthyl 6-(2-anilino-2-oxoethyl)-1-benzothiophene-2-carboxylateHCID 57443967—

Reaction Steps

[2-(ethoxycarbonyl)-1-benzothien-6-yl]acetic acid (0.2 g, 0.757 mmol), EDCI (0.22 g, 1.15 mmol) and HOBt (0.16 g, 1.18 μmmol) were stirred in DMF (6 mL) for 10 minutes before adding aniline (85 mg, 0.913 mmol). The solution was stirred at room temperature for 3 days. The solvent was removed in vacuo and the residue partitioned between H2O-EtOAc. The aqueous phase was extracted with further portions of EtOAc. The combined organic extracts were washed with brine, dried over MgSO4 and concentrated in vacuo. Et2O was added and the resulting beige solid collected by filtration to give the product. 1H NMR (DMSO-d6) δ 10.21 (s, 1H), 8.15 (s, 1H), 7.96 (s, 1H), 7.95 (d, J=8.4 Hz, 1H), 7.57 (d, J=7.8 Hz, 2H), 7.42 (dd, J=8.4, 1.2 Hz, 1H), 7.27 (t, J=7.2 Hz, 2H), 7.01 (t, J=7.2 Hz, 1H), 4.32 (q, J=7.2 Hz, 2H), 3.78 (s, 2H), 1.31 (t, J=7.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834034B2
Source datasetuspto-grants-2010_11
ORD IDord-78a61a6c6e3347f79cea910c489ab178
Source noteuspto-grants-2010_11