HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128588Generated: October 26, 2026
1,2-Dichloroethane → 1-(2-Methoxy-4-(1-acetyl-4-piperidyloxy)phenylacetyl)-4-(2-methylphenyl)-piperazine-2-carboxamide
https://huagongshe.com/reaction/128588
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Carbamoyl-4-(2-methylphenyl)piperazine | HCID 15430568 | — |
| Reactant | 2-Methoxy-4-(1-acetyl-4-piperidyloxy)phenylacetic acid | HCID 53759817 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(2-Methoxy-4-(1-acetyl-4-piperidyloxy)phenylacetyl)-4-(2-methylphenyl)-piperazine-2-carboxamide | HCID 53658220 | — |
Reaction Steps
2-Methoxy-4-(1-acetyl-4-piperidyloxy)phenylacetic acid (35 mg, 0.11 mmol), 4-(2-methylphenyl)piperazine-2-carboxamide (25 mg, 0.11 mmol), EDC (28 mg, 0.15 mmol), and HBT (17 mg, 0.13 mmol) were combined in DMF (4 ml) under nitrogen. The mixture was rendered basic by addition of triethylamine (0.043 ml) and stirred at ambient temperature for 18 hours. The mixture was concentrated in vacuo and the residue was chromatographed on silica gel eluted with 2% methanol in methylene chloride. The combined product fractions were evaporated to dryness in vacuo and the residue was rechromatographed on silica gel eluted with 96:4:0.4 methylene chloride:methanol:concentrated ammonia. The combined product fractions were evaporated to dryness in vacuo and the residue was concentrated from methanol and ether to give 1-(2-methoxy-4-(1-acetyl-4-piperidyloxy)phenylacetyl)-4-(2-methylphenyl)-piperazine-2-carboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05464788 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-337256f47c4246ae986cc83b56554282 |
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| Source note | uspto-grants-1995_11 |
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