HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292362Generated: October 31, 2026
1,2-Dichloroethane → HCID 18914177, compound
https://huagongshe.com/reaction/1292362
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(2-Ethylphenyl)piperazine | HCID 2736460 | — |
| Reactant | HCID 18914153 | HCID 18914153 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18914177 | HCID 18914177 | — |
Reaction Steps
To a stirred solution of 1-(2-ethylphenyl)piperazine (0.19 g; 1.0 mmol), 4-(5-benzimidazolylcarbonylamino)phenylacetic acid (0.329 g; 1.10 mmol), HOBT (0.14 g; 1.0 mmol), and EDC (0.230 g; 1.20 mmol) in DMF (30 mL) was added DIEA (0.23 mL; 1.3 mmol). The reaction was stirred at ambient temperature for 18 h and the solvent was evaporated under reduced pressure. The residue was partitioned between CH2Cl2 and saturated aqueous NaHCO3. The organic phase was separated and washed with saturated aqueous NaHCO3 and brine. The organic phase was dried (MgSO4), filtered, and the solvent was evaporated under reduced pressure. The residue was purified by pressurized silica gel column chromatography using 93:7:0.35 CH2Cl2 :MeOH:NH4OH as eluant. Evaporation of the product-containing fractions under reduced pressure gave the title compound as an amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05756504 |
|---|
| Source dataset | uspto-grants-1998_05 |
|---|
| ORD ID | ord-70322005fbb14f3392ca94d99752f3bb |
|---|
| Source note | uspto-grants-1998_05 |
|---|