HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576161Generated: October 30, 2026
1,2-Dichloroethane → (4-Amino-2-(trifluoromethyl)phenyl)(4-ethylpiperazin-1-yl)methanone
https://huagongshe.com/reaction/576161
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1-Ethylpiperazine | HCID 79196 | — |
| Reactant | 4-amino-2-(trifluoromethyl)benzoic Acid | HCID 3836325 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-Amino-2-(trifluoromethyl)phenyl)(4-ethylpiperazin-1-yl)methanone | HCID 90417522 | 89.2% |
Reaction Steps
A mixture of 4-amino-2-trifluoromethyl-benzoic acid (15 g, 73.1 mmol), HOBT (14.56 g, 95 mmol), EDC (16.82 g, 88 mmol), Et3N (20.38 mL, 146 mmol), 1-ethyl-piperazine (8.35 g, 73.1 mmol) in DCM (200 mL) was stirred at 25° C. for 2 h. To the mixture was added DCM (200 mL) and then washed with H2O, 2 mol/L NaOH (2×150 mL) and brine. The organic layer was dried over Na2SO4 and concentrated to give a off white solid of (4-amino-2-trifluoromethyl-phenyl)-(4-ethyl-piperazin-1-yl)-methanone (20 g, 65.2 mmol, 89.0% yield): 1H NMR (400 MHz, CDCl3) δ: 7.07 (d, J=8.0 Hz, 1H), 6.92 (d, J=2.4 Hz, 1H), 6.79 (dd, J=2.0, 8.0 Hz, 1H), 3.99 (s, 2H), 3.84-3.76 (m, 2H), 3.25-3.23 (m, 2H), 2.50-2.39 (m, 4H), 2.33-2.31 (m, 2H), 1.08 (t, J=7.2 Hz, 3H); ES-LCMS m/z 302 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09035063B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-245a17f3a9404d0ca4bd63b93db1e26f |
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| Source note | uspto-grants-2015_05 |
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