HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500667Generated: October 26, 2026
Aniline → Ethyl 6-(2-anilino-2-oxoethyl)-1-benzothiophene-2-carboxylate
https://huagongshe.com/reaction/500667
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | [2-(Ethoxycarbonyl)-1-benzothien-6-yl]acetic acid | HCID 59424238 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 6-(2-anilino-2-oxoethyl)-1-benzothiophene-2-carboxylate | HCID 57443967 | 66.2% |
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 mmol) 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 0.17 g of product (66%). 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07772238B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-f0d0072c114348aa81ef211532132299 |
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| Source note | uspto-grants-2010_08 |
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